Shinaj

Photoinduced Excited State Processes in
Carbonylpyrenes: A Comparison between Solution

and Solid-State Properties
A thesis submitted for the degree of
Doctor of Philosophy
in the
School of Chemistry
by
Shinaj K. R.
Indian Institute of Science Education and Research

Thiruvananthapuram
Thiruvananthapuram – 695016
Kerala, India
September 2016
Declaration
I hereby declare that the work reported in this thesis is original and was carried out
by me during my tenure as a Ph. D. student at the School of Chemistry, Indian Institute
of Science Education and Research Thiruvananthapuram. Such material as has been
obtained from other sources has been duly acknowledged in the thesis.
Place: IISER Thiruvananthapuram Shinaj K. R.

Date: 30-09-2016
Certified that the work incorporated in this thesis “Photoinduced Excited State
Processes in Carbonylpyrenes: A Comparison between Solution and Solid-State
Properties” submitted by Shinaj K. R. was carried out by the candidate under my
supervision. This thesis has not formed the basis for the award of any degree, of any
university or institution.
Place: IISER Thiruvananthapuram Dr. Mahesh Hariharan

Date: 30-09-2016 (Thesis supervisor)
Dedicated To…
My Beloved family
ACKNOWLEDGEMENTS
The thesis dissertation marks the end of a long and eventful journey for which there are
many people that I would like to acknowledge for their support along the way.
First and foremost, I would like to express my special appreciation and thanks to my
advisor Dr. Mahesh Hariharan, for his constant guidance and support, and for providing
excellent research environment during the six years of my doctoral study. His advice on both
research as well as on my career have been invaluable. He gave me the freedom to pursue my
interests, simultaneously keeping me on the research track. I am extremely thankful to him for
his enormous help, discussions without any limit, constant guidance and support throughout
my Ph. D. work. He has constantly encouraged me to push my limits farther and farther. It is
indeed a rare privilege to work under his guidance.
My sincere thanks to Prof. V. Ramakrishnan and Prof. E. D. Jemmis, present and former
Directors of IISER-TVM, for allowing me to use the facilities of IISER to carry out my research
work. I am grateful to my doctoral committee members, Prof. K. George Thomas, Dr. Kana M.
Sureshan, Dr. Hema Somanathan and Dr. V. Sivaranjana Reddy for their support, guidance
and helpful suggestions. I extend my gratitude to all my Ph. D. course instructors. I thank all
the faculty members of IISER Thiruvananthapuram for all the support and motivation.
It is my pleasure to express my sincere thanks to Dr. Suresh Das, former director, NIIST
Trivandrum for allowing me to use the experimental facilities in his institute. I express my
sincere gratitude to Mr. Robert, Mr. Kiran and Mr. Chandran, NIIST Trivandrum for TEM
and SEM microscopic imaging at NIIST.
I am deeply indebted to all my present and past group members: Dr. Rijo T. C., Mr. Ajith
R. Mallia, Mr. Kalaivanan N., Mr. Abbey M. Philip, Ms. Somadrita, Dr. Salini, Dr. Nandita
G. Nair, Mr. Nagaraj, Ms. Gopika Gopan, Ms. Remya Ramakrishnan, Ms. Shubhasmin Rana,
Ms. Amalu Mohan, Mr. Ebin Sebastian and Ms. Anusha Thampi for their help and fruitful
discussions during my Ph. D. work. During the course of my Ph. D. work, I had the pleasure
of working with several project students. Their assistance during the presented work is
gratefully acknowledged.
I would like to thank several people who made this work possible, and who have made my
stay at IISER-TVM enjoyable. I remember the first Ph. D. batch students of IISER-TVM: Dr.
Manil, Dr. Atchuth Rao, Dr. Vidyasgar, Dr. Pratap Zalake, Dr. Priyakumari, Dr. Subila, Dr.
Deepthi, Dr. Jissy and Dr. Vidya for the harmony and support. Special thanks to Mr. Baiju P.
K., Mrs. Reshmi Thomas, Dr. Anoop Thomas and Dr. Gireesh K. K., who were always there
for any help and warm company. I am deeply grateful to Mr. Sandeep, Dr. Shymala, Ms. Shine
K. Albert, Ms. Sabnam Kar, Ms. Jiji, Ms. Rohini, Mr. Mohan, Mr. Soumik, Mr. Purnachandra
Rao, Ms. Hema, Ms. Hemna, Mr. Hari, Mr. Amol and Mr. Murali for their support and
affection. I thank all my friends in Techies’ park hostel especially Mr. Sankaran N., Mr.
Santhosh, Mr. Haris, Mr. Febin and Mr. Sujith for their support, love and care.
I take this opportunity to express my immense gratitude towards all my teachers in St.
Thomas College, Thrissur for the motivation to keep high standard in my life during my
graduation studies. I am thankful to all my teachers in CUSAT for helping me to pursue my
passion for research during my master’s graduation. I also thank them for the continuous
support and care that they have provided me since my M.Sc. days. Thanks to all my M.Sc.
colleagues for their support and care during my doctoral program.
I thank to Dr. V. Sivaranjana Reddy for the TDDFT calculations. My wholehearted

thanks goes to Mr. Alex Andrews for single crystal X-ray diffraction measurements and
helping me with various software. I express my sincere thanks to Prof. Babu Varghese, IIT-
Madras, who had helped with solving some of the crystal. I thank him for the fruitful
discussions and valuable suggestions we had with him. I extend my sincere thanks to Mr.
Adarsh for NMR experiments, Mr. Aneesh for SEM analysis and Mr. Nibith, Mr. Shiju, Mr.
Manoj for GC-mass, elemental and IR analysis. I thank Mr. Shebin George for the graphical
artworks.
I would like to thank my friends outside IISER: Dr. Jimil George, for standing by me
through the good and the bad times and eternally reminding me to believe in myself; Karthika,
for her immense belief in my abilities and for constantly reminding me of the greener sides of
life. Without her I would have struggled to find the inspiration and motivation needed to
complete this dissertation.
I am indebted to Council of Scientific and Industrial Research (CSIR) and Department

of Science and Technology (DST), Government of India, and IISER-TVM for the financial
assistance. I thank them for ensuring a continuous funding during my doctoral study.
Above all, I would like to acknowledge the tremendous sacrifices that my parents made
to ensure that I had an excellent education. For this and much more, I am forever in their debt.
It is to them that I dedicate this dissertation.
Shinaj K. R.
Preface
Understanding the electronic communication between chromophores in complex
molecular architectures is a key factor for designing and construction of functional
photonic devices. Such correlation is based on interchromophoric electronic coupling
which mediates electron and/or excitation energy transfer. In addition to
interchromophoric electron/energy transfer processes, there are intrachromophoric
radiationless transitions which compete with the former. Advanced spectroscopic
techniques can be employed to monitor the ultrafast molecular dynamics arising from
the interplay between electronic and vibronic relaxation mechanisms in
multichromophoric systems.
Investigating the influence of crystal packing on the device performance is
essential to design new promising materials. Despite the advancement in
experimental and theoretical methods, the structure-property correlation in molecular
solids is not well understood. The solid-state packing of the organic semiconductors
depends on the nature of substituents and electronic distribution in the aromatic core.
However, it is extremely difficult to predict the solid-state order of the crystal
engineered molecules since small chemical modifications can cause huge differences
in the solid-state organization. Investigation on the influence of solid-state packing on
charge transport properties should be carried out using molecules that are as similar
as possible in terms of molecular formula, type of intermolecular interactions and
electronic properties. Ideally, they should differ in crystal packing, in order to
understand the underlying aspects of charge mobility through the crystal system.
Pyrene is the fruit fly of photochemists. Its unique properties have inspired
researchers from many scientific areas, making pyrene the chromophore of choice in
fundamental and applied photophysical research. Since the discovery of excimer
formation by Förster and Kasper in 1954, pyrene has been used as a chromophore in
various charge and energy transfer systems. Despite the vast number of pyrene based
donor (D)-acceptor (A) systems reported, the study of excited state dynamics of
pyrene is still a burgeoning topic of interest.
The light-emitting behaviour of molecular solids differs from that of dilute
solutions because emission in the solid-state is dictated by the whole collective rather
than by individual molecules. Studying molecular crystals provides essential
information on how molecules are arranged with respect to their neighbours and
interactions that bind them together which is required to correlate the crystal packing
with emission characteristics. Polyaromatic hydrocarbons are generally characterized
by herringbone packing due to CHedge-to-face interactions. However, a
dramatic reduction in the edge to face interaction promotes for enhanced overlap
through face to face geometry generating slipped stack, brickwork and cofacial
packing. Various covalent and noncovalent routes have been employed to tune the
solid-state luminescent properties to obtain the desired emitting characteristics.
Covalent routes includes changing the number and position of alkoxy substituents
and alkyl chain length while noncovalent routes involve polymorphism, phase
transition, nano/microcrystal forms and multi-component systems.
A brief illustration of the i) unique photophysical properties of pyrene
chromophore ii) an overview on the structure-property correlation in molecular solids
and iii) investigating the influence of crystal packing on the device performance is
provided in Chapter 1.
Despite of the versatility and the simplicity of the molecular structure, pyrene
shows complex intramolecular photophysical properties. The intermolecular energy
redistribution after excitation to higher electronic states involves strong vibronic
couplings of the electronic states leading to an ultrafast internal conversion (Sn→S1)
that has been measured to be within 150 fs. All these processes, ultimately lead to a
fluorescence contribution originating from the excited singlet state. Hence a lot of
studies were focused to understand the ultrafast internal conversion processes within
first hundreds of femtoseconds after excitation. It is well-known that carbonyl
functional groups exhibit a degree of spin–orbit coupling at the carbonyl oxygen that
allows for intersystem crossing, generating triplet state (Tn). Albeit, widely
investigated, the understanding about the photophysics of carbonylpyrenes is greatly
limited to their characteristic singlet emission properties. Investigation of ultrafast
excited state dynamics of this family of chromophores is significant in understanding
fundamental energy/electron transfer phenomena. In Chapter 2, we present
quantitative studies of the excited-state dynamics of carbonyl-functionalized pyrene
derivatives by using broadband transient absorption spectroscopy.
Molecular crystal engineering of polyaromatic hydrocarbons to yield 1–2D
lamellar arrangement demonstrated a pivotal role in photonic and semiconductor
device applications. Extended orbital overlap through-columnar stacks compared to
a herringbone arrangement of arenes proved to be vital. Recent efforts in transforming
the herringbone to the columnar arrangement of arenes through various methods
such as chemical modifications, co- and solvent-crystallization, heat mode mechanical
stimulation and solid seeding have proven to be effective. Achieving a diverse degree
of orbital overlap between the neighbouring units in the crystalline state is still a
challenging task. We modulated the extent of  overlap between vicinal pyrene
units through successive acylation. Unprecedented heteropolar dihydrogen contacts
(sp2 C–HH–C sp3) in organic crystals are established using QTAIM. Hirshfeld
surface analysis is indicative of an increase in  interactions and a concomitant
decrease in the  interactions with an increase in the number of acetyl groups per
pyrene unit. A combination of C–HH–C, C– HO and  interactions facilitate
the transformation of sandwich herringbone packing of pyrene to the herringbone
arrangement and the brickwork arrangement and finally to columnar stacks. A
systematic decrease in the interplanar angle between the vicinal pyrene units could be
attributed to the dramatic shift in the emission spectra (ca. 42–174 nm) of crystalline
acetylpyrenes when compared to pyrene. J-like aggregation and/or aggregation
induced emission (AIE) in the crystal packing of acetylpyrenes corroborates the
moderately emissive blue–green–orange crystals. While in another context, the extent
of orbital overlap (π–π) between vicinal pyrene units in crystalline 1–4BP was
regulated by exploiting the steric hindrance offered via successive benzoylation.
Progressive increment in the steric hindrance causes an increase in the
transverse/longitudinal displacement of the vicinal pyrene units. As a result, a 48-fold
reduction in the π-stacking between pyrene units was observed in tetrabenzoylpyrene
with respect to monobenzoylpyrene. Moderating the molecular stacking along with
crystal induced emission (CIE) through arrested intramolecular rotations of pendent
benzoyl groups may give rise to green-yellow-orange solid-state emitters. In Chapter
3, we tuned the extent of  overlap between vicinal pyrene and achieved diverse
degree of orbital overlap between the neighbouring units in the crystalline state.
Molecular ordering in organic single crystals plays a substantial role in the
performance characteristics of electronic devices, such as organic field-effect
transistors (OFFTs) and organic light-emitting diodes (OLEDs). Systems that can
exhibit 1D and 2D conductivity are highly desirable for the fabrication of devices.
Chapter 4 explores the effects of packing on charge mobility in systematically
synthesized acetylpyrene derivatives. Single crystal FETs were fabricated using the
top-contact, bottom-gate geometry and at increasingly negative gate voltages, the
mobility was found to monotonously increase from 0.03 to 0.18 cm2 V-1 s-1.
Contents
List of Figures
List of Tables
List of Schemes
1. Solid-state organization and photophysics of pyrene
1.1. Introduction 19
1.2. Chemical modifications of pyrene 20
1.3. Introduction to the photophysics of pyrene 22
1.3.1. Molecular dynamics revealed by transient spectroscopy 23

1.4. Solid-state organization and optical properties 24
1.4.1.  interactions in polynuclear aromatic hydrocarbons 25
1.4.2. Tuning solid state luminescence: Structure  optical property 27
relationships
1.4.2.1 Covalent routes to tune the optical properties 28
1.4.2.2 Non-Covalent routes to tune the optical properties 29
1.4.2.2.1. Polymorphism 30
 Extent of -overlap and conformation differences 30
 Excited state intramolecular proton transfer 31
(ESIPT)
1.4.2.2.2. Stimuli responsive phase transition and 32
fluorescence switching
 Temperature-responsive materials 33
 Multiple-stimuli responsive materials 34
1.4.2.2.3. Crystal to amorphous transformation and emission 36
switching
 Amorphization by shear stress 36
1.4.2.2.4. Multicomponent systems to tune the emission 38
properties
1.5. Overview of optical behaviour of aggregate states 39
1.6. Electronic and optoelectronic organic devices 42
1.6.1. Organic Field Effect Transistors 43
1.7. Objective of the thesis 46
2. Vibronically accelerated intersystem crossing competes with internal
conversion in acetylpyrenes
2.2. Synthesis, characterization and crystallization of acetylpyrene 49
derivatives (1-4AP)
2.3. Results and Discussions 50
2.3.1. Frontier molecular analysis and steady state absorption and 50
emission measurements
2.3.2. Nanosecond transient studies 57
2.3.3. Femtosecond transient studies 60
2.3.4. TDDFT calculation and Jablonski diagram 65
2.4. Conclusion 67
2.5 Appendix 68
3. Engineering the solid-state packing of carbonylpyrenes via C–HH–C, C–
HO and – interactions for tuning opto-physical properties
3.2.1 Synthesis, crystallization and thermal analysis 79
2.3.2. QTAIM and Hirshfeld Analyses 82
2.3.3. Crystal structure analyses of 1-4AP 86
2.3.4. Steady-state absorption and emission measurements 92
3.2.5. Synthesis and crystallization 98
2.3.1. Frontier molecular analysis and steady state studies 99
2.3.2. Crystal packing of 1-4BP 107
2.3.8 Photophysical properties of crystalline 1-4BP 110
3.4. Conclusion 116
3.5 Appendix 117
4. Solid-state ordering of pyrene based single crystalline materials for high-
performance organic field-effect transistors
4.2.1. Synthesis, characterization and crystallization of bis-haloacetyl 132
pyrene derivatives (XPs)
4.2.2. Crystal structure analyses of XPs 133
4.2.3. Hirshfeld surface analysis 145
4.2.4. Morphological Analysis 149
4.2.5. Conductivity measurements and theoretical calculations 154
4.3. Conclusion 157
4.4. Appendix 159
6. Bibliography 168
7. List of publications 183
8. Presentations at conferences 184
9. Copyrights and permission 185
List of Figures
Figure Title Page
1.1. Depiction of pyrene (A) according to Clar’s sextet rule; (B) nomenclature 20
of positions; (C) K-region and non-K-region of pyrene; (D) functionalized
at the active positions (1, 3, 6, 8-positions) by single bond connection; (E)
fused at the K-region and (F) fused at the non-K-region.
1.2. Shows (A) mirror plane three chemically distinguishable sites; (B); (C) 21
and (D three main groups of chemically identical sites.
1.3. (A) Absorption and emission spectra of pyrene in methanol and (B) 22
Scheme showing the relaxation processes of pyrene after photoexcitation
to the S2 state. IC: internal conversion, IVR: internal vibrational relaxation
1.4. Pictorial representation of the A) herringbone; B) sandwichherringbone; 25
C) gamma () and D) beta () packing motifs.
1.5 Bar chart representation of the ratios of (%CH)/(%CC) interactions 26
and the corresponding packing motifs of PAHs.
1.6. Show (A) Molecules under investigation; (B) Normalized fluorescence 28
spectra of thin films of MBC12 (blue spectrum), DBC12 (yellow
spectrum), and TBC12 (green spectrum). ex = 360 nm. The corresponding
fluorescence as visualized on excitation with a 365 nm UV light is also
shown.
1.7. Shows (A) Tetramer and trimer assemblies in ANP polymorphs and 31
photographs of corresponding crystals, excited under UV light (ex = 365
nm); (B) Variations in extent of -overlap and corresponding crystal
emission colour in ANP derivatives.
1.8. ESIPT-induced emission switching in 2-(2’-hydroxyphenyl)-imidazo[1,2- 32
a]pyridine.
1.9. (A) Herringbone to brickstone structural transformation in BC8; (B) 34
Thermochromic transformations in AA1 and AA2.
1.10. Schematic representation of (A) mechanisms for fluorescence at the cost 35
of frustrated [2 + 2] cycloaddition in CN(L)-TrFMBE; (B) Different modes
of slip-stacking in DBDCS molecular sheets; thermo/piezochromic
switching between green and blue forms. SEM images show
corresponding changes on the crystal surface.
1.11. Stimuli-induced switching of solid-state emission by (A) TPE-Py; (B) 37
hemicyanin dye; and (C) DPATPAN.
1.12. The emission switching observed in (A) 1,4-bis-p-cyanostyrylbenzene by 39
means of co-crystallization; (B) Fluorescence switching in CDPA by
means of formation of multicomponent systems using acid–base
interactions.
1.13. Schematic diagram showing the formation of H- and J-aggregates with 40
their possible electronic transitions.
1.14. Definition of (A) pitch (P) and roll (R) angles and associated distances 41
and vectors. The labels x and y refer to the directions of the short and
long molecular axes, respectively. (B) View along the short molecular
axis of a “pitched” -stack and along the long molecular axis of a “rolled”
-stack. Schematic representation of “pitch” and “roll” angles/distances
(P/dP; R/dR) and the structural description of Herringbone as well as H-
and J-aggregates in terms of relative translation of molecules. Insets A
and B represent pitch and roll inclinations that lead to J-aggregate and
Herringbone
1.15. Common OFET configurations employed: (A) top contact and (B) bottom 44
contact.
1.16. Schematic representation of the (A) HOMO and LUMO of the organic 45
semiconductor with respect to the source-drain metal Fermi level; (B)
Theoretical transport properties from a p-type OFET.
2.1. Row I: Schematic molecular structure and Row II: ORTEP diagram of the 50
crystal structure of 1-4AP derivatives.
2.2. Illustrations of the frontier molecular orbitals of i) 1AP; ii) 2AP; iii) 2’AP; 51
iv) 2’’AP; vi) 3AP and vii) 4AP evaluated at the B3LYP/6-311G*++ from
crystal structure.
2.3. Shows A) Cyclic voltammograms of 1-4AP derivatives in CH3CN and B) 52
Energy level diagram for 1-4AP derivatives as calculated using TD-DFT
(B3LYP/6-311G*++)
2.4. Shows the normalised (A) absorption and (B) fluorescence spectra of 1- 53
4AP (0.1-1 M) derivatives in CHCl3.
2.5. Shows fluorescence decay profile of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 56
2”AP; (E) 3AP and (F) 4AP in CHCl3 at the respective emission maximum
(exc=375 nm).
2.6. nTA spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP 57
derivatives in CHCl3.
2.7. SVD of nanosecond transient spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 58
2”AP; (E) 3AP and (F) 4AP derivatives in CHCl3.
2.8. SVD of nanosecond transient spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 58
2”AP; (E) 3AP and (F) 4AP derivatives in CHCl3.
2.9. Show A) Variation of triplet lifetime and B) triplet quantum yield of 1- 59
4AP in CHCl3.
2.10. fTA spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP 60
2.11. Transient absorption spectra for 4AP as plotted in the early time delay 61
where at 3.5 ps a growth around 500 nm is observed.
2.12. SVD of fTA spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and 62
(F) 4AP in CHCl3.
2.13. Right singular vectors obtained from global analyses for (A) 1AP; (B) 62
2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP in CHCl3.
2.14. (A) Representative phosphorescence spectrum of 4AP in CHCl3 recorded 64
at 77 K (ex = 380 nm; dotted graph represents the fluorescence spectrum
of 4AP); (B) Phosphorescence decay of 1-4AP derivatives in CHCl3
recorded at 77 K (ex = 380 nm).
2.15. Overlay of nTA spectra (blue trace) and fTA spectra (red trace) of (A) 65
1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP in CHCl3.
2.16. Decay profile of S4 state of 2’’AP and 4AP; Potential energy cuts along 66
C=O symmetric stretch vibrational mode of singlet excited states and
triplet excited state of B) 2’’AP and C) 4AP.
2.17. Jablonski diagram depicting the photophysics of acetylpyrene. 66
3.1. Volume calculated for (A) pyrene and (B) benzoyl unit in 1BP from 78
Crystal Explorer 3.0.
3.2. Row I: molecular structure of 1–4AP; Row II: corresponding single 79
crystal X-ray structure. Photographic image of the crystals Row III: in
daylight; and row IV: under UV illumination. X-ray structure of P is
taken from the literature.
3.3. Shows (A) DSC melting temperature (Tm); (B) near-linear increment in 81
the melting temperature (Tm) and (C) linear increment in the ΔH values
of crystalline 1-4AP derivatives.
3.4. Shows QTAIM electron density map of (A) 2AP; (B) 3AP and (C) 4AP, 84
arrows indicate the existence of intermolecular C–HH–C contacts.
3.5. Hirshfeld 2D fingerprint plot of 4AP with the region of the plots 85
corresponding to (A) CC and (B) HH interactions; Hirshfeld surface
of 4AP mapped with dnorm depicting (C) CC and (D) HH
interactions; (E) percentage contribution of edge-to-face (CH) and
face-to-face (CC) interactions in 1–4AP.
3.6. Close packing arrangement in 1–4AP indicating the values of 87
[(%CH)/(%CC)]. Herringbone (> 4.5), sandwich herringbone
(3.2 < < 4.0), (1.2 < < 2.7),  (0.46 < < 1.0).
3.7. Shows (A) the gradual decrease in the interplanar angle between the 87
nearest molecules; (B) the decreasing angle and the consequent increase
in stacking of the pyrene units in the crystalline 1-4AP.
3.8. Shows the torsional angle between adjacent pyrene units in crystal 89
packing of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP.
3.9. Shows the aerial overlap between adjacent pyrene units in close packing 90
of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP.
3.10 Shows the C–HO interactions in the crystal packing of (A) 2AP; (B) 91
2’AP; (C) 2”AP; (D) 3AP and (E) 4AP.
3.11. Shows fluorescence decay profile of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 93
2”AP; (E) 3AP and (F) 4AP in CHCl3 solution on exciting at 375 nm and
collected at different wavelengths.
3.12. Shows the fluorescence excitation spectra of (A) 1AP; (B) 2AP; (C) 2’AP; 93
(D) 2”AP; (E) 3AP and (F) 4AP in CHCl3 as compared to absorption
spectrum.
3.13. Concentration dependent emission spectra of (A) 1AP; (B) 2AP; (C) 95
2’AP; (D) 2”AP; (E) 3AP and (F) 4AP in CHCl 3 solution on exciting
at 350 nm.
3.14. Concentration dependent excitation spectra of (A) 1AP; (B) 2AP; (C) 95
2’AP; (D) 2”AP; (E) 3AP and (F) 4AP in CHCl3 solution while monitoring
at 500 nm (for 1AP and 2”AP) and 550 nm (for 2AP, 2’AP, 3AP and 4AP).
3.15. Shows the normalised (A) Absorption and (B) fluorescence emission 96
spectra of crystalline 1-4AP derivatives; excitation wavelength is 350 nm;
(C) fluorescence decay profile of crystalline 2-4AP derivatives and the
corresponding inset shows fluorescence decay profile of crystalline 1AP,
excitation wavelength is 375 nm and emission monitored at 518 nm
(1AP); 602 nm (2AP); 567 nm (2’AP); 631 nm (2”AP); 645 nm (3AP) and
646 nm (4AP) and (D) CIE colour diagram of fluorescence emission for
crystalline 1-4AP derivatives.
3.16. Shows fluorescence excitation spectra of crystalline (A) 1AP; (B) 2AP; (C) 97
2’AP; (D) 2”AP; (E) 3AP and (F) 4AP as compared to absorption spectra.
Absorption spectra of crystalline 1-4AP derivative are reproduced for
comparison with excitation spectra. Emission maxima, where the
excitation spectra are monitored, are indicated in the bracket.
3.17. Row I: Molecular structure of 1–4BP; Row II: close packing arrangement 99
in the crystal (a) 1BP; (b) 2BP; (c) 2’BP; (d) 2’’BP; (e) 3BP and (f) 4BP; Row
III: photographic image of the crystals in daylight (above) and under UV
illumination (below).
3.18. (A) Frontier molecular orbital (FMO) analysis of 1–4BP calculated from 101
the B3LYP/6-311G**+ level of theory. Lower and upper plots represent
the HOMOs and LUMOs, respectively (B) Cyclic voltammograms of 1–
4BP in acetonitrile; (C) Absorption spectra of 1– 4BP; the area filled
spectrum (grey) represents the absorption spectrum of pyrene and (D)
Nanosecond transient absorption spectrum of 4BP in chloroform.
3.19. Shows the (A) fluorescence spectra; ex =380 nm, area filled graph (grey 106
colour) represent the emission spectrum of pyrene in CHCl3 (B)
fluorescence decay; ex = 375 nm and (C) phosphorescence spectra; ex =
380 nm of 1-4BP derivatives in ethanol.
3.20. Shows the gradual increase in the traverse/longitudinal shift between 108
nearest pyrene molecules in the crystalline 1-4BP derivatives.
3.21. Shows the aerial overlap between adjacent pyrene units in close packing 108
of (A) 1BP; (B) 2BP; (C) 2’BP; (D) 2”BP; (E) 3BP and (F) 4BP.
3.22. Shows the C–HO interactions in the crystal packing of (A) 1BP; (B) 110
2BP; (C) 2’BP; (D) 2’’BP; (E) 3BP and (F) 4BP.
3.23. (A) Absorption; (B) fluorescence spectra of crystalline 1–4BP derivatives; 111
λexc = 380 nm.; the area filled spectrum (grey) represents the absorption
and emission spectra of crystalline pyrene(C) fluorescence decay profile
of crystalline 1-4BP; exc =375 nm and emission wavelength monitored
(D) CIE colour diagram of fluorescence emission for crystalline 1-4BP
derivatives.
3.24. Shows fluorescence excitation spectra of crystalline (A) 1BP; (B) 2BP; (C) 113
2’BP; (D) 2”BP; (E) 3BP and (F) 4BP as compared to absorption spectra.
Emission maxima, where the excitation spectra are monitored, are
indicated in the bracket.
3.25. (A) Indicates F (major component; □); F (●) of 1-4BP in the crystalline 114
state; F (‫ )٭‬of 1-4BP in solution state and % CC interaction (; ∆)
obtained from Hirshfeld analysis (Table 3.13) and B) Jablonski diagram
depicting energy levels in solution (monomeric) and aggregated
(crystalline) state in 1BP.
3.26. Energy levels diagram of monomer and dimer of 1BP and 4BP calculated 115
from B3LYP/6-311G**++ level of theory.
4.1. Single crystal X-ray structure of XPs. 133
4.2. (A) Decrease in the intramolecular dihydrogen distance in 1,3-XP 135
compared to 1,3-AP and (B) QTAIM electron density map of 1,3-BP
indicating intramolecular dihydrogen and C-HO interactions.
4.3. Close packing arrangement in (A) 1,3-XPs and (B) 1,8-XPs indicating the 137
values of  [(%CH)/(%CC)]. Herringbone ( 4.5), sandwich
herringbone (3.2 4.0),  (1.2 2.7),  (0.46 1.0) and (C)
schematic representation showing the decrease in the interplanar
distance between pyrene units in 1, 3-XPs.
4.4. Shows the decrease in the interplanar distance between pyrene units in 137
1,3-XP.
4.5. Calculated ESP maps of representative monomers of A) 1,3-XP and B) 139
1,8-XP from crystal structure. All maps used consistent surface potential
ranges [−4.75e-2 au (red) to 4.75e-2 au (blue)] and an isovalue of 0.000400
au.
4.6. Intermolecular interactions in 1,3-XPs. (A) Intermolecular C-HF and 140
C-HO interactions in 1,3-FP; (B) C-HO and C-HCl interactions in
1,3-CP; (C) C-HBr and C-HO interactions in 1,3-BP and (D) C-HI,
C-Iπ C-HO and ππ interactions in 1,3-IP.
4.7. Shows QTAIM electron density map of 1,3-IP, arrows indicate the 141
existence of intermolecular I contacts.
4.8. Intermolecular interactions in 1,8-XPs. (A) Intermolecular C-FC, 142
C−Hπ and C-HF interactions in 1,8-FP; (B) C-HCl and C-HO
interactions in 1,8-CP; (C) C-HH-C, and C-HO interactions in 1,8-
CP and (D) C-HH-C and C-Brπ interactions in 1,8-BP.
4.9. Shows the decrease in the interplanar distance between pyrene units in 142
1,8-XP.
4.10. Shows QTAIM electron density map of 1,8-FP, arrows indicate the 143
existence of intermolecular CF interactions.
4.11. QTAIM electron density map of (A) 1,8-CP and (B) 1,8-BP indicating 144
intermolecular interactions.
4.12. Hirshfeld 2D fingerprint plot of 1,3 and 1,8-XPs. 145
4.13. Row I: chemical structure of 1–4 AP; Row II: stereo microscopic images 148
of corresponding single crystal Row III: schematic drawing that depicts
the possible crystal packing pattern and the range of =
(%CH)/(%CC) contact ratio for each packing.
4.14. SEM images of A) 1AP; B) 2AP; C) 2’AP; D) 2”AP; E) 3AP and F) 4AP, 149
drop casted in benzene.
4.15. Show the AFM images of A) 1AP; B) 2AP; C) 2’AP; D) 2”AP; E) 3AP and 151
F) 4AP, drop casted in benzene.
4.16. Show the laser confocal images of a) 1AP; b) 2AP; c) 2’AP; d) 2”AP; e) 152
3AP and f) 4AP, drop casted in benzene.
4.17. Show the TEM images of a) 1AP; b) 2AP; c) 2’AP; d) 2”AP; e) 3AP and f) 153
4AP, drop casted in benzene.
4.18. I-V profile determination by A) drop-casting the derivatives in benzene; 154
B) single crystal and C) single crystal organic field-effect transistor
(OFET) measurement on 4AP.
List of Tables
Table Title Page
2.1. Electrochemical experimental and calculated energy levels of 1-4AP 52
derivatives.
2.2. Photophysical properties of 1-4AP derivatives in CHCl3. 53
2.3. Excitation energy, oscillator strength, main transition orbital, and their 54
contribution calculated for 1-4AP derivatives using TD-DFT (B3LYP/6-
311G*++).
2.4. Lifetimes of 1-4AP obtained from global analyses of fTA spectra (exc=400 63
nm).
3.1. Shows crystallographic data and refinement parameters for crystalline 1- 80
4AP derivatives.
3.2. Shows melting temperature (Tm) and change in enthalpy (ΔH) values for 81
crystalline 1-4AP derivatives.
3.3. Shows intramolecular (CH3) HH (aryl) (Å) distance (d) in crystalline 1- 82
4AP derivatives that is less than the sum of van der Waals radii of two
hydrogen atoms (2.4 Å).
3.4. Shows calculated topological properties of the electron density for the intra- 83
and intermolecular interaction in 2, 3 and 4AP derivatives.
3.5. Percentage of intermolecular contacts of a molecule in crystalline 1-4AP. 86
3.6. Interplanar angle between nearest pyrene molecules in crystalline 1-4AP. 88
3.7. Shows the photophysical properties of 1-4AP derivatives. 94
3.8. Shows crystallographic data and refinement parameters for 100
crystalline 1-4BP derivatives.
3.9. Experimental (electrochemical) and calculated energy levels of 1-4BP. 102
3.10. Excitation energy, oscillator strength, main transition orbitals and their 103
contribution calculated for 1-4BP using TDDFT (B3LYP/6-311G**++).
3.11. Shows the photophysical properties of 1-4BP derivatives. 105
3.12. Geometries in the face-to-face -stacked arrangements in crystalline 1-4BP. 109
3.13. Percentage of intermolecular contacts of a molecule in crystalline 1-4AP. 114
4.1. Crystal data and structure refinement for 1,3 and 1,8-XP. 134
4.2. Shows the intramolecular interactions in 1,3-XP and 1,8-XP as visualised 136
through Mercury CSD 3.8.
4.3. Calculated topological properties of the electron density for the 141
intermolecular interaction in XPs.
4.4. Shows the percentage of intermolecular contacts of a molecule in crystalline 146
XPs.
List of Schemes
Scheme Title Page
2.1. Shows the synthesis of acetylpyrene (1-4AP) derivatives. 72
3.1. Shows the synthesis of benzoylpyrene (1-4BP) derivatives. 123
4.1. Synthesis of 1,3- and 1,8-Bis(chloroacetyl)pyrene (1,3-CP and 1,8-CP). 163
4.2. Synthesis of 1,3- and 1,8-Bis(bromoacetyl)pyrene (1,3-BP and 1,8-BP). 164
4.3. Synthesis of 1,3- and 1,8-Bis(fluroacetyl)pyrene (1,3-FP and 1,8-FP). 165
4.4. Synthesis of 1,3- and 1,8-Bis(iodoacetyl)pyrene (1,3- and 1,8-IP). 166
Chapter 1
Solid-state organization and photophysics of pyrene
1.1. Introduction
Pyrene has been discovered by the french chemist Auguste Laurent in 1837 by
extraction from coal tar[1] but the correct chemical formula has been determined later
by Gräbe (1871)[2] and the structure by Bamberger and Philip in 1887[3]. Withal, the
found molecular formula remains still valid whereupon pyrene consists of 16 carbon
atoms within four rings forming the polycyclic aromatic hydrocarbon (PAH). The
view offered through Clar’s model claims pyrene can be drawn with two circles that
are cylindrically localized and two double bonds (Figure 1.1 A). Arising from this
description, pyrene appears as biphenyl annulated with two further rings in the
armchairs. Indeed, these double bonds at the centre exhibit increased reactivity
towards oxidation due to less stabilization although still being aromatic. The position
1, 3, 6, and 8 (non K-region) have been heavily exploited for syntheses of new extended
π-systems (Figure 1.1C, D&F)[4]. Recently, a few pyrene derivatives fused at the K-
region were developed (Figure 1E), and they exhibited interesting properties.
Since its discovery pyrene has predominantly attracted attention for its
outstanding photophysical properties, which is why pyrene is called “the fruit fly of
photochemists”[5]. Pyrene is well known for its long lifetime of the excited state of the
monomer in solution, high fluorescence quantum yields and the concentration
dependent shift of the emission spectrum upon excimer formation[6]. Monomeric

Chapter 1 – Solid-state organization and photophysics of pyrene 24
Ar
A) B) 2 C) D) Ar E) F)
1 3
10 4 Ar Ar
9 5
8 6
Ar
7
Non-K Region
K Region
Figure 1.1. Depiction of pyrene (A) according to Clar’s sextet rule; (B) nomenclature of
positions; (C) K-region and non-K-region of pyrene; (D) functionalized at the active positions
(1, 3, 6, 8-positions) by single bond connection; (E) fused at the K-region and (F) fused at the
non-K-region (Adapted with permission from ref. 4. Copyright © 2013, American Chemical
Society).
pyrene emits between 370 nm and 400 nm whereas emission of the excimer appears
red-shifted[7, 8]. These properties make pyrene one of the most frequently applied
fluorescence markers to monitor dynamics of polymer chains and protein
structures[9-12]. After selective cysteine labelling of proteins with N-(l-
pyreny1)maleimide the appearance or absence of the excimer signal provides
information about the spatial distance of labelled residues. The latter example shows
that no sophisticated chemistry is required for this application and the introduction of
functional groups at position 1 is already known for more than 70 years. Nevertheless,
chemists have greatly extended the variety of available protocols in the meantime to
functionalize pyrene for respective applications. Especially in the last decade a large
number of novel methods have been reported for making new classes of pyrene
compounds accessible for material applications.
1.2. Chemical modifications of pyrene

Pyrene has two mirror planes (one lies in the plane of the molecule) which divide
the molecule into four quarters with three types of positions which exhibit strong
difference in chemical reactivity(Figure 1.2A). Therefore, the overview about reported
chemical methods to substitute pyrene is grouped into “1,3,6,8”, “2,7” and “4,5,9,10”
regions. Reactivity of pyrene at 1, 3, 6 and 8 positions toward electrophiles arise from
the large orbital coefficients at these carbon atoms (Figure 1.2C). First protocols are
reported in 1937 by Vollmann et al. for the synthesis of mono-, di-, tri and tetra-
substituted pyrene derivatives[13]. Additionally, chemists have invented multistep
syntheses starting from benzene derivatives to achieve otherwise impossible
substitution of pyrene. 1-substituted and 1,3,6,8-tetrasubstituted pyrenes can be easily
accessible by direct electrophilic substitution of pyrene. The ease of preparation of
mono- and tetrasubstituted pyrenes combined with the relatively simple purification
gives the possibility to straightforwardly introduce pyrene into different molecular
architectures. On the other hand, the selective preparation of pyrenes is challenging
but simultaneously
A) B) C) D)
Figure 1.2. Shows (A) mirror plane three chemically distinguishable sites; (B); (C) and (D
three main groups of chemically identical sites.

highly required. It is crucial to obtain well-defined disubstituted pyrene building
blocks for the controlled synthesis of linear or cyclic oligomers as well as polymers
(Figure 1.2B&D).
1.3. Introduction to the photophysics of pyrene
Pyrene is an important polycyclic aromatic hydrocarbon[14, 15]. In 1954 Förster
and Kasper reported the first observation of intermolecular excimers in a pyrene
solution[16]. This excimer formation, combined with long-lived excited states, high
fluorescence quantum yield[17], exceptional distinction of the fluorescence bands for
monomer and excimer, and the sensitivity of its excitation spectra to
microenvironmental changes (Ham effect)[18] brought pyrene to the most explored
and well-studied organic molecule in terms of its photophysical properties.
Pyrene has its absorption in the UV spectral domain and shows distinct
electronic absorption bands (Figure 1.3A). Each electronic absorption band consists of
A) B)
Figure 1.3. (A) Absorption and emission spectra of pyrene in methanol and (B) Scheme
showing the relaxation processes of pyrene after photoexcitation to the S2 state. IC: internal
conversion, IVR: internal vibrational relaxation (Adapted with permission from ref. 20.
Copyright © 2016 Elsevier).

a variety of vibrational modes that give rise to the structure in the absorption spectra
[19]. The S1 (1B3u) ← S0 (1Ag) absorption is weak compared to the absorption into
higher lying electronic states [e.g., S2 (1B2u) ← S0 (1Ag)] because this transition is
forbidden due to the symmetry of the states. When pyrene is excited to higher
electronic states (Sn, n>2) a fast (85 fs for the S2 state) internal conversion to the S1 state
occurs mediated by vibronic coupling of the electronic states (Figure 1.3B)[20].
Starting from the excited electronic S1 state multiple processes happen. They give rise
to signals detected in ultrafast spectroscopy. From the S 1 state intersystem crossing
(ISC), internal conversion (IC), and fluorescence are the pathways for the molecule to
relax to the ground state.
1.3.1. Molecular dynamics revealed by transient spectroscopy
The S1 excited state lifetime of pyrene dissolved in methanol for a concentration
of about 10-2 mM was measured to 339 ns and the fluorescence quantum yield to
0.75[21]. These values are observed to be concentration dependent. This means that
the non-radiative relaxation processes or intersystem crossing to the T 1 state are slow
compared to the fluorescence. All these processes are fairly slow compared to internal
conversion from the S2 state or vibrational relaxation in the S1 state and only give rise
to negligible constant contributions on the ps time scale of the measurements. Foggi
and co-workers [22]directly observed that the S2 to S1 internal conversion which occurs
within 150 fs measured by femtosecond transient spectroscopy in solution. They
found that the rate of formation of the S1 state is a function of the electronic state
excited. For excitation of higher electronic states, the formation of the S1 state had a
longer time constant (about 400 fs when excitation of the S 4 state). The time constant
of the internal vibrational excess energy redistribution after formation of the S1 state
was found to be about 4 ps for all measurements exciting different electronic states.
1.4. Solid-state organization and optical properties
Light-emitting molecular solids and their potential utility in optical devices,
sensors and biological imaging has catalysed its emergence as an area of topical
research with a spectrum of prolific activities. The light emitting behaviour molecular
solid differ from that of dilute solution because emission of the solid-state is dictated
by the whole collective rather than by individual molecules. Studying molecular
crystals provides essential information on a) how molecules are arranged with respect
to their neighbours in solid-state, b) weak interactions that bind them together and c)
conformational preferences required to correlate the structural facts with several
macroscopic properties, including their emission characteristics. Such systematic
knowledge pertaining to how complex properties emerge from collections of
molecules and how sensitive these properties are to specific molecular ordering in
solids, could be translated to deriving new strategies to control molecular
arrangement, to tune solid-state luminescent properties and also to obtain multi-
colour emission[23]. Noncovalent routes inclusive of polymorphism, phase transition,
nano/microcrystal forms and multi-component systems, have evolved as an efficient
method to draw such correlations with a minimum number of variables[24-26]. Also
it provides an opportunity to enhance the utility of a molecule of interest by

generating a wide range of solid forms and with added scope for tailoring the
emission characteristics.
1.4.1. – interactions in polynuclear aromatic hydrocarbons
Polynuclear aromatic hydrocarbons (PAHs) are well-known to crystallise in four
possible structural motifs: herringbone, sandwichherringbone, – and –structures
(Figure 1.4)[27-29]. Each motif is associated with a particular -interaction geometry.
The herringbone motif is constructed from edge-to-face interactions while offset
stacking, as well as edge-to-face interactions, are observed in the sandwich
herringbone motif where molecules stack in pairs. In the –motif, molecules form
infinite stacks (offset and/or face-to-face) along one axis and a form of herringbone
(edge-to-face) along another axis. The graphitic type layering assembly that arises in
the –motif is promoted primarily by face-to-face or offset stacking of the molecules.
Because PAHs consist exclusively of carbon and hydrogen atoms, there are only three
A) B)
C) D)
Figure 1.4. Pictorial representation of the A) herringbone; B) sandwichherringbone; C)
gamma () and D) beta () packing motifs.

possible types of interatomic interactions: CC, HH and CH. The CC
interactions are optimised between parallel molecules stacked at van der Waals
separation distances, whereas the CH interactions are more effective between
inclined molecules[28]. It therefore follows that the – and –structures are rich in
CC interactions, CH interactions are more prevalent in the herringbone motif,
and both types of interactions are observed to a similar extent in the sandwich
herringbone arrangement[28]. These observations prompted Desiraju and
Gavezzotti[27-29] to investigate the molecular free surfaces of such molecules and the
contributions of molecular areas to the final packing arrangement; atoms located at
the core of the molecule, as well as a few peripheral carbon atoms, promote stacking
(layering) while the remaining atoms facilitate glide (herringbone) packing.
In order to evaluate the packing motifs of aromatic molecules in crystals, Barbour
and co-workers[30] proposed a quantitative analysis to classify the crystal structure to
a particular packing motif. In order to assess the packing motif of the crystal structure,
the relative contribution of each intermolecular interaction were determined and
finally calculate ratios of these interactions (%CH /%CC). The herringbone
structures all have (%CH/%CC) ratios greater than 4.5, sandwich motifs are in the
  Sandwichherringbone Herringbone
0 1 2 3 4 5 6 7 8 9 10
Figure 1.5. Bar chart representation of the ratios of (%CH)/(%CC) interactions and the
corresponding packing motifs of PAHs.

range of 3.2–4.0; –motifs in the range 1.2–2.7 and –motifs fall in the range between
0.46–1.0 (Figure 1.5).
1.4.2. Tuning solid-state luminescence: Structure  optical property relationships
Several approaches are being sought to modify the fluorescence wavelength and
intensity in the solid-state (state in which compounds are intended to be used)
aggregate suspensions, thin films or crystalline materials. Though our molecular level
awareness on the structure–property relationship in terms of optical properties is
fairly well established, the perception on factors that precisely control bulk or
supramolecular properties is still hazy. In organic materials, modification or alteration
of chemical structures is a common approach to tune solid-state luminescence
properties. For example, number and position of alkoxy substituents and alkyl chain
length direct the molecular packing and consequently their fluorescence properties in
diphenylbutadienes[31]. However, several limitations inherent to covalent synthesis
and solid-state reactions make dynamic tuning or switching of solid-state
luminescence a formidable target. Also because solid-state luminescence depends
strongly on the intermolecular dipole coupling, resulting from the relative
arrangements of neighbouring molecules and orientations of their dipole moments, it
is difficult to expect similar properties in related molecules. Looking beyond the
covalent routes that involve chemical modifications (synthetic tailoring of fluorophore
cores), recent developments in the modulation of materials properties via non-
covalent routes such as polymorphism (through conformational/packing changes),
phase transition (structural changes while maintaining the molecular integrity),

amorphization (disrupting the long-range molecular ordering) and preparation of
multi-component systems (controlling fluorophore aggregation) look promising.
1.4.2.1. Covalent routes to tune the optical properties
Several design strategies have been developed to alter the packing of organic
molecules, such as extension of π conjugation to enhance the π−π interactions between
adjacent molecules through chemical modification which includes incorporation of
heteroatoms into the conjugated backbone to provide more non-covalent interactions
(e.g., SS and N−Hπ interactions), and substitution with bulky groups. A detailed
study on the photophysical properties of a series of alkoxy substituted
diphenylbutadienes in solution and in the solid-state providing a molecular level
understanding of the factors controlling their solid-state luminescence behaviour is
reported by Suresh Das and co-workers[31](Figure 1.6A). The role of the number of
A) B)
Figure 1.6. Shows (A) Molecules under investigation and (B) Normalized fluorescence spectra
of thin films of MBC12 (blue spectrum), DBC12 (yellow spectrum), and TBC12 (green
spectrum). ex = 360 nm. The corresponding fluorescence as visualized on excitation with a 365
nm UV light is also shown (Adapted with permission from ref. 31. Copyright © 2008,
American Chemical Society).

alkoxy substituents and the alkyl chain length in controlling the nature of the
molecular packing and consequently their fluorescence properties has been
elucidated. Whereas in the di- and tri-alkoxy substituted derivatives, the solid-state
fluorescence was independent of the length of the alkyl chains, in the monoalkoxy
substituted derivatives, increasing the length of the alkyl chain resulted in a visual
change in fluorescence from green to blue. On the basis of the analysis of the molecular
packing in the single crystals, this difference could be attributed to fluorescence
arising from aggregates with an edge-to-face alignment in the molecules possessing
short alkyl chains (methyl and butyl) to monomer fluorescence in the long alkyl chain
containing derivatives (Figure 1.6B).
1.4.2.2. Non-Covalent routes to tune the optical properties
The utility in attaining the desired compounds through covalent synthesis is a
tedious task which makes it as an inefficient technique to tune the solid-state
properties. The solid-state luminescence within the chemically related molecules will
vary depending on the intermolecular dipole coupling, resulting from the relative
arrangements of neighbouring molecules and orientations of their dipole moments
therefore it is difficult to expect similar properties. Looking beyond the synthetic
tailoring of fluorophore cores (covalent routes) that involve chemical modifications,
recent developments in the modulation of materials properties via non-covalent
routes such as polymorphism (through conformational/ packing changes), phase
transition (structural changes while maintaining the molecular integrity),

amorphization (disrupting the long-range molecular ordering) and preparation of
multi-component systems (controlling fluorophore aggregation) look promising.
1.4.2.2.1. Polymorphism
McCrone defined a polymorph as “a solid crystalline phase of a given compound
resulting from the possibility of at least two different arrangements of the molecules
of that compound in the solid-state”[32]. This indicates that there are many ways in
which molecules can arrange[33], while confining near-optimal packing. However,
regardless of the degree of unpredictability, polymorphism offers an incomparable
multitude of opportunities in material modifications and property modulations,
without changing the molecular integrity[34]. Polymorphs often differ in their
physico-chemical properties such as melting point, crystal shape, colour, chemical
reactivity, dissolution rate, and solubility[35].
 Extent of -overlap and conformation differences
In organic functional materials varied molecular arrangements based on the
collective interactions, -overlap geometries and co-planarity of adjacent -planes
could lead to different extent of electronic conjugation and solid-state emission
characteristics[36, 37]. For example, five luminescent polymorphic form of 3(5)-(9-
anthryl)pyrazole (ANP) exhibit distinct crystal packing by tuning the intermolecular
interactions and hence the molecular assembly in the crystal structure (Figure 1.7A)
[38]. Further to the hydrogen bond types, the emission colours of the crystal forms
were correlated with the extent of – interactions: that with no interaction i.e. anthryl
rings are well outside their van der Waals distance from each other (blue emission);
A)
B)
Figure 1.7. Shows (A) Tetramer and trimer assemblies in ANP polymorphs and photographs
of corresponding crystals, excited under UV light (ex = 365 nm) (Adapted with permission
from ref. 38. Copyright © 2006, John Wiley and Sons) and (B) Variations in extent of -overlap
and corresponding crystal emission colour in ANP derivatives (Adapted with permission from
ref. 39. Copyright © 2009, American Chemical Society).
with strong interaction i.e. close face-to-face contacts between anthryl rings exist in
their crystals (green emission), and with weak interaction i.e. characterized by weak
 interactions between anthryl rings (blue-green emission). A series of 9-
anthrylpyrazole derivatives were designed and synthesized and depending on the
varying -overlap of anthracene-arrangement, different emission colors were
produced (Figure 1.7B)[39]. The emission colors of crystalline samples are strictly
related to the intermolecular packing degree of the anthracene moieties: the larger
overlapping area, the greater red shift of emission peak.
 Excited state intramolecular proton transfer (ESIPT)
A novel and effective mechanism of switching organic solid-state luminescence

Figure 1.8. ESIPT-induced emission switching in 2-(2’-hydroxyphenyl)-imidazo[1,2-
a]pyridine (Adapted with permission from ref. 41. Copyright © 2008, John Wiley and Sons).
based on an excited-state intramolecular proton-transfer (ESIPT) process[40] with
resultant changes in dipole moment are a good route to achieve switchable emission
colour and intensity. Interconversion of the crystal forms of 2-(2’-
hydroxyphenyl)imidazo[1,2-a]pyridine by a thermal dry process realized switching
of ESIPT luminescence between blue-green and yellow emission and also leads to
differences in molecular conformations and modes of packing (Figure 1.8)[41].
Similarly, 2-(2-hydroxyphenyl)-4(3H)-quinazolinone (HPQ) exhibits emission by
ESIPT to form dimorphs with different conformational twist[42]. The conformational
twist between the phenyl and quinazolinone rings of HPQ leads to different molecular
packing in the solid-state, giving structures that show solid-state fluorescence at 497
and 511 nm.
1.4.2.2.2. Stimuli responsive phase transition and fluorescence switching
Stimuli responsive phase transition and the resultant changes in fluorophore
arrangements has been actively investigated and is saturated with opportunity to

obtain multi-colour emission by fluorescence switching[43]. However, the design and
synthesis of organic materials that display efficient and reversible switching between
two luminescent states in the solid-state still remain a challenge. This can be mainly
attributed to the fact that the conversion of molecular structures in the solid-state is
often very difficult, making the controlled and reversible switching of solid-state
luminescence between polymorphs rather exceptional[44]. Based on the type of
stimuli, the materials are broadly classified as mechanochromic or piezochromic
(mechanical shock)[45], thermochromic (temperature)[46], solvatochromic
(solvent)[47] and vapochromic (vapour) materials[48].
 Temperature-responsive materials
Phase transition induced by temperature modulation provides an excellent
method to switch the solid-state emission of molecular materials. Structural
modulation brought through thermally reversible transformation between two
polymorphic states of octyloxy cyano substituted diphenylbutadiene (BC8)
possessing visually distinguishable fluorescence (Figure 1.9A)[49]. Melting results in
disruption of the weak hydrogen bonds causing the molecule to move out of its
interdigitated array and form separate layers of unidirectionally oriented molecular
stacks. As a result, the -stacks move closer to each other resulting in the formation of
J-aggregates which exhibit green fluorescence. The slow recovery of the stable blue
fluorescing state can then be attributed to a movement of the molecules within the
crystal lattice to regain the original crystal structure, causing the interdigitation of the
alkyl chains possibly due to the reformation of the weak hydrogen bonds.
Diethyl-2,5-bis(4-(trifluoromethyl)phenylamino)terephthalate (AA1) and
diethyl-2,5-bis(3,5-bis(trifluoromethyl)phenylamino)terephthalate (AA2) exhibit
(Figure 1.9B) thermally induced reversible phase transformations accompanied by
emission switching[44]. When heated below the melting point at (144 °C), red emitting
crystals of AAI (Form-I; λmaxem = 581 nm) exhibit thermochromic transformation to a
yellow solid (Form-II; λmaxem = 545 nm); similarly AA2 crystals transform from red
(Form-I; λmaxem = 610 nm) to green emitting form (Form-II; λmaxem = 503 nm) at 124 °C.
In both cases the emission switching involves the change from the H-aggregation
state, which can lead to the red shifts of emissions spectra due to exciton
delocalization, to the J-aggregation state. The reverse transitions occur, however, only
after the compounds melt.
A) B)
Figure 1.9. (A) Herringbone to brickstone structural transformation in BC8 (Adapted with
permission from ref. 49. Copyright © 2004, Royal Chemical Society) and (B) Thermochromic
transformations in AA1 and AA2 (Adapted with permission from ref. 44. Copyright © 2009,
John Wiley and Sons)
 Multiple-stimuli responsive materials
Molecular compounds that undergo phase transition in response to multiple

stimuli with associated changes in emission characteristics are suitable for developing
stimuli-responsive light emitting materials that have potential for various
applications. The type of stimuli possible for ensuing emission switching are
temperature, pressure and solvent vapour induced transformations[50-52].
Non-fluorescent asymmetric crystalline cyanostilbene derivative (Z)-3-(3′,5′
bis(trifluoromethyl)biphenyl-4-yl)-2-((4′-trifluoromethyl)biphenyl-4-yl)acrylonitrile
[CN(L)-TrFMBE] produces tightly packed π-dimer systems exhibiting reversible [2 +
2] cycloaddition with characteristic fluorescence modulation (Figure 1.10A)[53]. The
CN(L)-TrFMBE π dimer crystals are not at all fluorescent initially but switch to a
highly fluorescent state (ΦPL=24%) when an external shear-strain and/or prolonged UV
A) B)
Figure 1.10. Schematic representation of (A) mechanisms for fluorescence at the cost of
frustrated [2 + 2] cycloaddition in CN(L)-TrFMBE (Adapted with permission from ref. 53.
Copyright © 2009, American Chemical Society) and (B) Different modes of slip-stacking in
DBDCS molecular sheets; thermo/piezochromic switching between green and blue forms. SEM
images show corresponding changes on the crystal surface (Adapted with permission from ref.
54. Copyright © 2010, American Chemical Society).

(365 nm) irradiation is applied. The close pairs of stilbenic (C=C) bonds (∼3.8 Å) due
to the antiparallel π dimers in the pristine crystal become perturbed under applied
stimuli hence fluoresce with strong sky-blue emission at the cost of frustrated [2+2]
cycloaddition. Similarly, cyanostilbene-based [(2Z,2’Z)-2,2’-(1,4-phenylene)bis(3-(4-
butoxyphenyl))acrylonitrile (DBDCS)] highly luminescent molecular sheets which
exhibit two-color fluorescence switching in response to pressure, temperature, and
solvent vapor were reported (Figure 1.10B)[54]. Thermal annealing at 125 C leads to
sliding of molecular sheets along the shorter axis of DBDCS to initiate a phase
transition with resulting shift in solid-state emission from green light (λmaxem = 533 nm)
to blue (λmaxem = 458 nm). Rough and sheet-like regular surface projections on the
transformed crystals further validates the layer-sliding mechanism. Form-II solid
reverts to Form-I under shear stress and this two-colour fluorescence switching allows
the fabrication of a poly(methyl methacrylate)–DBDCS blend film for rewritable
fluorescent optical recording.
1.4.2.2.3. Crystal to amorphous transformation and emission switching
Crystal to amorphous conversion involves the transformation of a stable phase
to one less stable. Amorphous phase being a high energy phase, amorphization
requires the free energy of the crystal to be raised above to that of the amorphous
phase and also involves destruction of the regular lattice arrangement by means of
mechanical energy input or quench melting[55-58].
 Amorphization by shear stress
A heteroatom-containing luminogen (TPE-Py) obtained by melding a pyridinium

unit with tetraphenylethene through vinyl functionality under the shear stress caused
transformation of crystalline phase to a non-ordered amorphous phase. The solid-
state emission of TPE-Py can be reversibly switched between green and red color by
grinding–fuming and grinding–heating processes with a high contrast due
to the transformation from the crystalline to the amorphous state and vice versa
(Figure 1.11A) [59]. Melding a benzothiazolium unit with tetraphenylethene generates
a new hemicyanine luminogen, exhibiting crystochromism and its solid-state
emission can be repeatedly tuned from yellow or orange to red by grinding–fuming
or grinding–heating processes due to the transformation from the crystalline to the
A)
B)
C)
Figure 1.11. Stimuli-induced switching of solid-state emission by (A) TPE-Py (Adapted with
permission from ref. 59. Copyright © 2013, Royal Society of Chemistry); (B) hemicyanin dye
(Adapted with permission from ref. 60. Copyright © 2012, Royal Society of Chemistry) and
(C) DPATPAN (Adapted with permission from ref. 61. Copyright © 2013, Royal Society of
Chemistry).
amorphous state and vice versa (Figure 1.11B)[60]. Switching of emission colour from
green (λmaxem = 500 nm) to yellow (λmaxem = 551 nm) with amorphization in DPATPAN,
is an illustrative example in the context of tuning the solid-state emission by
amorphization through shear stress (Figure 1.11C)[61].
1.4.2.2.4. Multicomponent systems to tune the emission properties
Supramolecular luminescent systems composed of two or more organic
components provides a versatile approach to tuning and switching solid-state
luminescence by controlling the molecular organization through weak
interactions[62]. When compared to the synthetic point of view, this supramolecular
approach is an easy method and highly desirable technique, and offers a wealth of
opportunity for simple variation (by modifying one of the co-crystallization
components) and excellent scope for tuning the solid-state luminescence by control of
the solid-state structure[63].
The optical properties (such as UV-Vis absorption, luminescence emission, color,
lifetime, quantum yield) in an organic solid chromophore, stilbene derivative, 1,4-bis-
p-cyanostyrylbenzene (A) can be finely modified by supramolecular cocrystal
formation (Figure 1.12A)[64]. By selecting the co-formers with different potential
halogen or hydrogen bond interaction modes with the cyano group in A, six cocrystal
systems have been synthesized, providing multi-color fluorescent organic materials.
Effect of the nature of interactions and the molecular reorganization in the crystal
lattice by cocrystallization is further evident from the large solid-state emission

A)
B)
Figure 1.12. The emission switching observed in (A) 1,4-bis-p-cyanostyrylbenzene by means
of co-crystallization (adapted with permission from ref. 64. Copyright © 2011, John Wiley and
Sons) and (B) Fluorescence switching in CDPA by means of formation of multicomponent
systems using acid–base interactions (adapted with permission from ref. 65. Royal Society of
Chemistry).
switching observed in the molecular complexes of 2-cyano-3(4-
(diphenylamino)phenyl)acrylic acid (CDPA) with organic amines (Figure 1.12B)[65].
Tuning and switching of the luminescence is demonstrated by exposing powdered
CDPA to amine vapor (pyrrolidine, morpholine) and HCl solution.
1.5. Overview of optical behaviour of aggregate states
The π-conjugated molecules in solution or amorphous or crystalline solid-state
exhibit two distinct types of aggregate namely J- and H-aggregates. The J-aggregates
(J for Jelly who discovered the phenomenon of J-aggregates) show bathochromic shift
(red shift) and H-aggregate show hypochromic shift (blue shift) in absorption spectra
in comparison to the monomer spectra. The exciton theory is developed by Micheal
Kasha[66], describes the correlation between structure of aggregates and their
absorption spectra. According to exciton theory, dye molecules are considered as
point dipoles and upon aggregation the excited state split into two levels one being
higher in energy and the other being lower in energy compared to the monomeric
excited state (Figure 1.13). The allowed and forbidden transitions of the electron are
governed by the tilt or slip angle (α) which is the angle between the transition dipole
moments and the line joining the centres of the molecule. In the case of J-aggregates
having head to tail arrangement of molecules (α < 54°), the allowed transition is to the
lowest excited state which results narrow red shifted emission (Figure 1.13). But in the
case of H-aggregate having face to face or sandwich type of molecular arrangement
(α > 54°), the allowed transition is to the upper excited state level which results blue
shifted emission (Figure 1.13)[67].
M2
M1 M1 M2
m>0 m=0
S1
Energy
m=0 m>0
S0
H-aggregate Monomer J-aggregate
Figure 1.13. Schematic diagram showing the formation of H- and J-aggregates with their
possible electronic transitions.

Curtis and co-workers[68] analyzed solid-state packing through the inclinations
in given -stack describing the inclination by two angles, called “pitch (P) and roll
(R)” from an “ideal” cofacial -stack (H-aggregate). The “pitch” inclinations describe
translation of adjacent molecules relative to one another in the direction of the long
molecular axis, while the “roll” inclinations that along the short molecular axis. Figure
A) B)
C)
Figure 1.14. Definition of (A) pitch (P) and roll (R) angles and associated distances and
vectors. The labels x and y refer to the directions of the short and long molecular axes,
respectively; (B) View along the short molecular axis of a “pitched” -stack and along the long
molecular axis of a “rolled” -stack and (C) Schematic representation of “pitch” and “roll”
angles/distances (P/dP; R/dR) and the structural description of Herringbone as well as H- and
J-aggregates in terms of relative translation of molecules. Insets A and B represent pitch and
roll inclinations that lead to J-aggregate and Herringbone (Adapted with permission from ref.
68. Copyright © 2004, American Chemical Society).

1.14A shows the definitions of the pitch and roll angles. Let the x-y plane be parallel
to the molecular plane of a molecule in a -stack. The vectors, x and y, represent the
short and long axes of the molecule, respectively, and they are perpendicular to each
other. The shortest distance between the planes of the two adjacent molecules in the
-stack is defined by a vector, d, which is perpendicular to the molecular plane (Figure
1.14B). Moderately large pitch distortions preserve - interactions between adjacent
molecules (J-aggregation), whereas roll translations greater than 2.5 Å lead to
minimum -overlap (Herringbone-type) (Figure 1.14C). Compared to the cofacial -
stacked structure in H-aggregates, translation of molecules along the long molecular
axis leads to a head-to-tail arrangement with an enhanced delocalization of electronic
excitation over several molecules due to a significant retention of -overlap between
neighbouring molecules. Such structural variations in molecular aggregates have
profound influence on their fluorescence properties such as emission wavelength and
efficiency.
1.6. Electronic and optoelectronic organic devices
The study of the influence of the crystal packing on the device performance is
essential to design new promising materials. The structure-property correlation is still
not well understood, although currently great efforts are being devoted in this
direction, both theoretically and with experiments. The solid-state packing of the
organic semiconductors depends on the nature of their conjugated electronically
delocalized core together with the substituents that they might bear. However, it is
extremely difficult to predict the solid-state order of the crystal engineered molecules
since small chemical modifications can cause a huge difference in the solid-state
organization. Ideally, the investigation of the influence of the solid-state packing on
the transport should be carried out in materials that are as similar as possible (i.e.,
molecular formula, type of intermolecular interactions, and electronic properties) and
that only differ in crystal structure.
1.6.1. Organic field effect transistors
The first germanium based device, the transistor invented by John Bardeen,
William Shockley and Walter Brattain (1947) is regarded as one of the greatest
discoveries of the 20th century since it is the basic component in modern electronics.
However, due to the fact that inorganic electronics have some technological
limitations associated with them, organic-based devices have recently emerged in the
market, beginning to replace amorphous silicon in some applications, and also have
great possibility to find their place in a wide range of new applications. One of their
main advantages is solution-processability, and thus, organic materials offer the
possibility to fabricate low-cost and flexible devices and are also suitable for large area
applications. This has been the motivation for why this field has been labeled “organic
and large area electronics (OLAE)”. In addition, the versatility of organic synthesis
allows for the preparation of materials according to promising properties. That is,
since by chemically modifying their molecular structure and functionality the solid-
state structure and the resulting macroscopic properties are altered, it is feasible to
synthesize tailored materials for specific uses.

The operation principle of an organic field-effect transistor (OFET) relies on the
application of an electric field that causes the formation of a conducting channel in the
dielectric/semiconductor interface. The two main configurations employed in OFETs
are depicted in Figure 1.15 and are known as top contact and bottom contact. In both
cases, the organic semiconductor deposited on a dielectric is contacted with two metal
contacts, namely, the source and drain, and on the other side of the dielectric a third
contact, the gate, is placed. Thus, the source-drain current (ISD) flowing along the
Figure 1.15. Common OFET configurations employed: (A) top contact and (B) bottom
contact.
organic material can be modulated by application of a gate voltage (VG) between the
source and the gate, which creates an electric field responsible for the formation of an
accumulation layer of charges at the semiconductor/dielectric interface. Also,
depending on the VG applied, the nature of the charge carriers accumulated at the
interface can be controlled, that is, holes (in p-type semiconductors) or electrons (in n-
type semiconductors). The voltage applied to the gate shifts the highest occupied
molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy
levels with respect to the metal Fermi level (EF) of the source-drain contacts, which
A) B)
LUMO
source HOMO drain
VG<0 VG>0
++++
----
source drain source drain
Figure 1.16. (A) Schematic representation of the HOMO and LUMO of the organic
semiconductor with respect to the source-drain metal Fermi level and (B) theoretical transport
properties from a p-type OFET.
allows for the formation of the conducting channel (Figure 1.16A). Hence, a negative
gate voltage shifts the orbitals up and might result in the alignment of the HOMO
with EF, making it possible to have hole conduction. Otherwise, if a positive gate
voltage is applied, the HOMO and LUMO will shift down, and if the LUMO becomes
resonant with EF, electrons will flow from the metal to the LUMO. However, one
should bear in mind that the orbital shifting induces bending of the bands near the
source-drain electrodes and, thus, there is an energy barrier at these contacts. The
calculated electrical characteristics obtained in an OFET are shown in Figure 1.16B. In
general, the OFET transport properties are described with two types of graphs. The
output characteristics correspond to the representation of the ISD versus the VSD at fixed
VG. In this plot, it is clearly observable that there are two regimes, the linear regime,
where the current is described by a parabola, and the saturation regime, where the
source-drain current is independent of the source-drain voltage. Additional
information can be extracted from the transfer characteristics, which plots the ISD with
the VG at fixed VSD. Here, the on/off ratio, which is the ratio of current in the
accumulation mode to the current in the depletion mode, and the threshold voltage
(VT), that is, the gate voltage from which the conduction channel starts to form, can be
easily visualized.
1.7. Objective of the thesis
Pyrene is considered to be the most intriguing polyaromatic hydrocarbons
(PAHs), due to its diverse photophysical properties. Upon photoexcitation, the energy
redistribution to lower electronic states involves strong vibronic couplings leading to
an ultrafast internal conversion (< 150 fs). All these processes, ultimately lead to
fluorescence originating from the lowest excited singlet state. As a result, most of the
studies were focused to understand the ultrafast internal conversion process in the
first hundreds of femtoseconds after excitation. The photoexcited ultrafast properties
in aromatic carbonyl compounds is generally rationalized by intersystem crossing,
internal conversion, and charge transfer processes. However, much less is known,
regarding the excited-state dynamics and relaxation mechanisms of carbonylpyrenes.
In Chapter 2, we try to decipher the excited state dynamics of a series of
carbonylpyrenes using ultrafast transient absorption studies. In Chapter 3, we
emphasize on the peripheral substitution of pyrene core through successive
acylation/benzoylation which cause a structure driven ordering in the crystalline state.
Such structurally driven approach hold promise for a detail understanding of the
intermolecular interactions which helps to regulate the arene-arene interactions in
fluorescent pyrene crystals. The recent interests in pyrene based semiconductors is
due to control over molecular architecture that can be achieved by modifying the
structure by varying the position of substitution on the pyrene ring. Conductivity

measurements in acetylpyrene crystals reveal that stacked packing (brickwork and
columnar) is better than herringbone packing for enhanced conductance. In Chapter
4, emphasis the control over morphology that can be achieved in acetylpyrene to form
microscale conducting materials and their potential application in optoelectronic
devices.
Chapter 2
Vibronically accelerated intersystem crossing competes with
internal conversion in acetylpyrenes
Abstract
Amongst polyaromatic hydrocarbons (PAHs), pyrene (P) is considered to be most
intriguing molecule, due to its diverse photophysical properties. The pyrenyl class of
chromophores has gained widespread attention from long-time owing to their robust nature,
high molar absorptivity, extensive derivatization possibilities and their applications as long-
lasting laser dyes, biological sensors and light harvesters for solar energy conversion. Despite
this versatility and the simplicity of the molecular structure, pyrene shows complex
intramolecular photophysical properties. The intermolecular energy redistribution after
excitation to higher electronic states involves strong vibronic couplings of the electronic states
leading to an ultrafast internal conversion (S1Sn) that has been measured to be within 150
fs. All these processes, ultimately lead to a fluorescence contribution originating from the
excited singlet state. Hence a lot of studies were focused to understand the ultrafast internal
conversion processes within first hundreds of femtoseconds after excitation. It is well-known
that carbonyl functional groups exhibit a degree of spin–orbit coupling at the carbonyl oxygen
that allows for intersystem crossing, generating triplet state (Tn). Albiet, widely investigated,
the understanding about the photophysics of carbonylpyrenes is greatly limited to their
characteristic singlet emission properties. Investigation of ultrafast excited state dynamics of
this family of chromophores is trivial in understanding fundamental energy/electron transfer
phenomena similar to that associated with excited state structural changes. In this chapter, we
present quantitative studies of the excited-state dynamics of carbonyl-functionalized pyrene
derivatives by using broadband transient absorption spectroscopy.
T 97%
ISC
Sn
Tn
T 38%
ISC S0
Sn Tn
S0
Chapter 2 – Vibronically accelerated intersystem crossing competes with internal conversion in acetylpyrenes 54
2.1. Introduction
Amongst polyaromatic hydrocarbons (PAHs), pyrene (P) is considered to be most
intriguing molecule, due to diverse photophysical properties[69, 70]. The pyrenyl
class of chromophores has gained widespread attention from the long-time owing to
their robust nature[71], high molar absorptivities, extensive derivatization
possibilities[4, 5, 72] and their applications as long-lasting laser dyes[73], biological
sensors[74, 75] and light harvesters for solar energy conversion[76]. Despite this
versatility and the simplicity of the molecular structure, pyrene shows a complex
intramolecular photophysical properties. The intermolecular energy redistribution
after excitation to higher electronic states involves strong vibronic couplings of the
electronics states leading to an ultrafast internal conversion (S nS1) that has been
measured to be 150 fs. All these processes, leading ultimately leads to a fluorescence
contribution originating from the excited singlet state (S2). Hence a lot of studies were
focused to understand the ultrafast internal conversion process in the first hundreds
of femtoseconds after excitation. The photophysical properties of most aromatic
carbonyl compounds have been generally rationalized by intersystem crossing[77],
internal conversion[78] and charge transfer[79]. However, much less is known,
regarding the excited-state dynamics and relaxation mechanisms of pyrene
chromophores functionalized with carbonyl groups.
It is well-known that carbonyls functional groups exhibit a degree of spin–orbit
coupling at the carbonyl oxygen that allows for intersystem crossing generating triplet
state (Tn). In particular, pyrene chromophore is associated with singlet state
photophysics. However, through the establishment of a gold(I)−carbon σ bond in
(phosphine)gold(I) pyrene derivatives, the singlet state photophysics normally
associated with the pyrene has been transformed to triplet state[80]. Similarly,
substitution of pyrene with a nitro group similarly leads to remarkable ISC rates[81].
Though pyrene carbonyls are widely investigated, but limits in understanding the
characteristic singlet emission properties (SnS1). Konishi and co-workers have
reviewed the photophysical properties of carbonyl-functionalized pyrene derivatives
[i.e., pyrene with aldehyde (1-formylpyrene), ketone (1-acetylpyrene), carboxylic acid
(1-pyrenecarboxylic acid), and ester groups (1-methoxycarbonylpyrene)] using a
measurement of absolute fluorescence quantum yield in various solvents and time-
dependent density functional theory (TD-DFT) calculations[82-84]. Investigation of
ultrafast excited state dynamics of this family of chromophores is trivial in
understanding fundamental energy/electron transfer phenomena like associated with
involving excited state structural changes. Here, we try to decipher the ultrafast
excited state dynamics of carbonylated pyrene derivatives. In this letter, we present
quantitative studies of the excited-state dynamics of carbonyl-functionalized pyrene
derivatives by using broadband transient absorption spectroscopy and an in-depth
global analysis of the observed kinetics. The observed ultrafast dynamics are
rationalize with time-dependent density functional theory calculations.
2.2. Synthesis, characterization and crystallization of acetylpyrene

derivatives (1-4AP)
Lewis acid-catalyzed (AlCl3) electrophilic aromatic substitution of acetyl group
on pyrene (P) in carbon disulfide (CS2) affords acetylpyrene derivatives (14AP) in
low to moderate yields (Scheme 1a, Row I)[13]. Adding a stoichiometric quantity of
acetyl chloride to a solution of pyrene and AlCl3 in CS2 at ambient temperature
rendered the desired acetylpyrene derivatives (14AP) (Figure 2.1, Row I)[85]. The
molecular structures were further confirmed through single crystal X-ray analysis
(Figure 2.1, Row II). Single crystals 1-3AP suitable for X-ray analysis were obtained by
slow evaporation from varying composition of chloroform:hexane mixture while 4AP
was obtained by temperature gradient cooling in chloroform.
I)
1AP 2AP 2’AP 2”AP 3AP 4AP
II)
Figure 2.1. Row I: Schematic molecular structure and Row II: ORTEP diagram of the crystal
structure of 1-4AP derivatives.
2.3. Results and Discussions
2.3.1. Frontier molecular analysis and steady-state absorption and emission
measurements
Frontier molecular orbital (FMO) analysis, cyclic voltammetric, UV-Vis
absorption and emission measurements were employed to investigate the extent of

electronic perturbations in P imparted by incremental acetyl groups. FMO analyses of
14AP shows that the electron density of HOMO is distributed in the P unit while the
electron density of LUMO is more delocalized with a considerable extension to the
carbonyl group(s) (Figure 2.2). Cyclic voltammetry was performed to investigate the
variations in the HOMO-LUMO gap due to incremental carbonyl groups on the
pyrene unit (Figure 2.3A). 1AP [0.1 M nBu4NPF6 in acetonitrile (ACN)], shows a
reversible reduction peak (Ered) at -1.562 V vs. SCE corresponding to one electron
reduction while oxidation peak appears at 1.483 V. The AP derivatives in ACN
displayed a systematic decrease in the reduction potential, from Ered = -1.562 V vs. SCE
for 1AP to Ered = -1.0 vs. SCE for 4AP. Decrease in the electrochemical gap (HOMO -
LUMO) of AP (3.045 eV for 1AP; 2.80 eV for 4AP; Table 2.1) in comparison to P (3.37
eV)[86] is in good agreement with the trend observed in the FMO analysis(Table 2.1).
i) ii) iii) iv) v) vi) vii)
LUMO+1
LUMO
Energy (eV)
HUMO
HUMO-1
Figure 2.2. Illustrations of the frontier molecular orbitals of i) 1AP; ii) 2AP; iii) 2’AP; iv)
2’’AP; vi) 3AP and vii) 4AP evaluated at the B3LYP/6-311G*++ from crystal structure.
A) B)
Figure 2.3. Shows A) cyclic voltammograms of 1-4AP derivatives in CH3CN and B) energy
level diagram for 1-4AP derivatives as calculated using TD-DFT (B3LYP/6-311G*++)
UV-Vis absorption spectra of spectra of 14AP in chloroform exhibit bands centered
around 286-298 and 359-407 nm respectively (Figure 2.4, Table 2.2)[85]. Successive
addition of acetyl groups on P core afforded a systematic spectral change with a
progressive red-shift (ca. 70 nm) in the absorption maximum of 4AP when compared
to P. Time-dependent density functional theory (TDDFT)[87, 88] calculations were
performed to examine the electronic transitions in 14AP derivatives (Table 2.3).
Table 2.1. Electrochemical experimental and calculated energy levels of 1-4AP derivatives.
Energy levels (eV) Energy levels (eV)

ox red
Eon Eon EHOMO ELUMO E EHOMO ELUMO E
(eV) a (eV) a (eV) a (eV) a (eV)a (eV)b (eV)b (eV)b
1AP 1.483 -1.562 -6.283 -3.238 3.045 -5.834 -2.278 3.555

2AP 1.579 -1.306 -6.379 -3.494 2.885 -6.044 -2.611 3.432
2’AP 1.578 -1.290 -6.378 -3.51 2.868 -6.064 -2.676 3.387
2’’AP 1.612 -1.344 -6.412 -3.456 2.956 -6.076 -2.704 3.372
3AP 1.724 -1.107 -6.524 -3.693 2.831 -6.260 -2.977 3.283
4AP 1.8 -1.0 -6.60 -3.80 2.80 -6.436 -3.241 3.194
a
experimental data; bcomputational data
A) B)
Figure 2.4. Shows the normalised (A) absorption and (B) fluorescence spectra of 1-4AP (0.1-
1 M) derivatives in CHCl3.
Low-lying excited electronic states mainly result from well- described*
transitions with a significant contribution from n* character. Figure 2.3B illustrates
the plot of the vertical excitation energies where the energy level ordering in the
singlet (S) and triplet (T) manifolds is shown. When compared to P, more
delocalization of the excited singlet (S2) is observed in 14AP with a decrease in the
Table 2.2. Photophysical properties of 1-4AP derivatives in CHCl3.

a abs 
a f 
a P  (ns)
a f 
a P 
a T 
a T
af aT
(nm) (nm) (nm) [Amplitude] (%) (nm) (nm) (s)
P 337 393 - 0.75 150.1 [100] - 415 11.0 38.0
1.39 [93]
1AP 359 412 520 0.004 12.7 450 4.85 52.30
0.98 [7]
1.39 [93]
2AP 373 426 520 0.008 9.8 450 5.76 90.09
0.65 [7]
1.3 [80]
2’AP 369 420 515 0.002 9.5 450 7.04 96.06
1.62 [20]
1.4 [97]
2”AP 375 413 520 0.008 11.3 490 10.13 94.53
0.6 [3]
3AP 388 431 525 0.003 1.2 9.4 490 11.08 96.45
4AP 407 435 520 0.002 0.98 11.4 500 12.16 97.03
achloroform solution; abs – absorption; f – fluorescence; - quantum yield; T- triplet
energy gap between S2-T4, bringing T4 triplet state nearly isoenergetic to S2 in 4AP.
Upon excitation at 350 nm, 14AP in chloroform shows bathochromic shift in the
emission maximum which is in accordance with observed redshift in the absorption
Table 2.3. Excitation energy, oscillator strength, main transition orbital, and their
contribution calculated for 1-4AP derivatives using TD-DFT (B3LYP/6-311G*++).
AP Excitation Oscillator Main

State Contribution
derivatives Energy (eV) strength (f) transition orbital
T4 3.5953 HOMO-1→LUMO 0.57309
T3 3.5686 HOMO→LUMO+2 0.51608
T2 3.4472 HOMO→LUMO+1 0.57142
T1 2.1566 HOMO→LUMO 0.68533

P
S4 4.6312 0.0000 HOMO-2→LUMO 0.68233
S3 4.3758 0.0000 HOMO→LUMO+2 0.68393
S2 3.7618 0.0003 HOMO→LUMO+1 0.52179
S1 3.6976 0.2523 HOMO→LUMO 0.66986
T4 HOMO→LUMO+1 0.50967
T3 HOMO-2→LUMO 0.47969
T2 HOMO-1→LUMO 0.50416
T1 HOMO→LUMO 0.68261
1AP
S4 4.2526 0.0189 HOMO-3→LUMO 0.53272
S3 3.6842 0.0250 HOMO-2→LUMO 0.47754
S2 3.5368 0.0042 HOMO-1→LUMO 0.48744
S1 3.3811 0.3305 HOMO→LUMO 0.66907
T4 3.2322 HOMO-2→LUMO 0.61257
T3 3.1466 HOMO-3→LUMO 0.55422
T2 2.9366 HOMO-1→LUMO 0.62909
T1 1.9407 HOMO→LUMO 0.68630

2AP
S4 3.5789 0.0014 HOMO-2→LUMO 0.55139
S3 3.5775 0.0175 HOMO-3→LUMO 0.63612
S2 3.3534 0.0103 HOMO-1→LUMO 0.60578
S1 3.2621 0.3659 HOMO→LUMO 0.67578

T4 3.2122 HOMO-3→LUMO 0.58217
T3 3.0649 HOMO-2→LUMO 0.56224
T2 2.9569 HOMO-1→LUMO 0.63426
T1 1.9112 HOMO→LUMO 0.68667

2’AP
S4 3.6180 0.0440 HOMO-3→LUMO 0.55533
S3 3.5039 0.0000 HOMO-2→LUMO 0.64427
S2 3.3982 0.0121 HOMO-1→LUMO 0.58073
S1 3.2178 0.4263 HOMO→LUMO 0.67433
T4 3.1900 HOMO-3→LUMO 0.57896
T3 3.0655 HOMO-2→LUMO 0.58915
T2 2.9120 HOMO-1→LUMO 0.61645
T1 1.9024 HOMO→LUMO 0.68751

2”AP
S4 3.5600 0.0023 HOMO-3→LUMO 0.64141
S3 3.4762 0.0186 HOMO-2→LUMO 0.54376
S2 3.3842 0.0122 HOMO-1→LUMO 0.56911
S1 3.2101 0.4039 HOMO→LUMO 0.67743
T4 3.0768 HOMO-3→LUMO 0.53675
T3 2.9932 HOMO-2→LUMO 0.53079
T2 2.8060 HOMO-1→LUMO 0.65503
T1 1.8452 HOMO→LUMO 0.68923

3AP
S4 3.4711 0.0127 HOMO-3→LUMO 0.58851
S3 3.3850 0.0091 HOMO-2→LUMO 0.58001
S2 3.2210 0.0174 HOMO-1→LUMO 0.62544
S1 3.1141 0.4384 HOMO→LUMO 0.67619
T4 3.0880 HOMO-3→LUMO 0.64605
T3 2.8940 HOMO-2→LUMO 0.60853
T2 2.6939 HOMO-1→LUMO 0.66586
T1 1.7869 HOMO→LUMO 0.69059

4AP
S4 3.3928 0.0000 HOMO-5→LUMO 0.65801
S3 3.2238 0.0000 HOMO-2→LUMO 0.67264
S2 3.0911 0.0234 HOMO-1→LUMO 0.65083
S1 3.0184 0.4624 HOMO→LUMO 0.67757

spectrum (Figures 2.4B). Low fluorescence quantum yield was observed for 14AP (f
 0.9%, Table S3; SI) in chloroform when compared with P (f = 75%)[89]. Pioneering
work by Foggi et al [22]on P have established that the excitation at 340 nm populates
the S2 state which undergoes ultrafast internal conversion (IC) to S1 state at a rate
constant of 150±50 fs. Subsequently, fluorescence is observed from S1 which forms the
primary decay pathway of the S2 with the remnants of excited singlet state (S1)
undergoing intersystem crossing to a triplet state. However in 14AP, strong mixing
of nearly-degenerate singlet and triplet states as elucidated from the relative energies
obtained from TDDFT calculations, brings efficient intersystem crossing (ISC) thereby
forming a competitive pathway for internal conversion (IC). Picosecond time-resolved
fluorescence measurement of 14AP in chloroform exhibits short singlet excited state
lifetime (f) in the range of 1–2 ns. (Figure 2.5, Table 2.2).
A) 10
5 B) 5
C) 10 5
10
4
Prompt Prompt Prompt
4
10 10
4
10
412 nm 426 nm 420 nm
3 3
10 10
3
10
Counts
Counts
Counts
2 2
10 10
2
10
1 1
10 10
1
10
0 0
0
10 10 10
0 10 20 0 10 20 0 10 20 30
Time (ns) Time (ns) Time (ns)
D) 5
10 E) 10 5
F) 5
10
Prompt Prompt
Prompt 4
4
10 10
4
430 nm 10 435 nm
413 nm
3
3
10 10
3
10
Counts
Counts
Counts
2
2
10 10
2
10
1
1
10 10
1
10
0
0
10 10
0
10
0 10 20 30 0 10 20 0 10 20
Time (ns) Time (ns) Time (ns)
Figure 2.5. Shows fluorescence decay profile of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E)
3AP and (F) 4AP in CHCl3 at the respective emission maximum (exc=375 nm).
2.3.2. Nanosecond transient studies
In order to explore the excited-state dynamics, nanosecond and femtosecond
transient absorption (nTA and fTA) techniques were employed to probe the events
after the photoexcitation of 14AP in chloroform. Figure 2.6 shows the nTA spectra of
1-4AP after laser excitation (355 nm, 40 mJ per pulse). Upon excitation at 355 nm, nTA
spectra for 1, 2 and 2’AP exhibit a transient absorption band centered at 450 nm with
a bleach in the region that corresponds to the ground state absorption. 2’’ and 3AP
features a transient absorption band centered at 490 nm whereas 4AP shows transient
absorption band at 500 nm. The transient absorption peak observed for 14AP
derivatives in chloroform were readily quenched by the dissolved oxygen which
strongly suggest that the transient species so formed after the nanosecond flash are
due to the triplet excited state of P (3P*; Figure S5; SI)[90]. Singular value
decomposition (SVD) of three dimensionalA versus time and wavelength spectral
A) 0 ns B) 0 ns
C) 0 ns
5 s 5 s 5 s
D) 0 ns E) F)
0 ns 0 ns
5 s
5 s 5 s
Figure 2.6. nTA spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP
data followed by global analyses were carried out to understand the principle
components responsible for the respective transient absorption spectra for 14AP
derivatives (Figure 2.7 and 2.8, Table S4; SI). SVD analyses of 1-4AP show only one
A) B) C)
0.4 0.4
V1 V1 0.30 V1
0.2 0.2 0.15
 O. D.
 O. D.
 O. D.
0.0 0.00
0.0
-0.15
-0.2 -0.2
-0.30
-0.4 -0.4
-0.45
360 420 480 540 600 660 360 420 480 540 600 660 360 420 480 540 600 660
Wavelength, (nm)
nm Wavelength, nm
D) Wavelength Wavelength (nm) F) Wavelength, nm
Wavelength (nm)
0.08
0.30 V1 V1 V1
0.30
0.06
0.15
0.15
 O. D.
0.04
 O. D.
 O. D.
0.00
0.00 0.02
-0.15
0.00
-0.30 -0.15
-0.02
360 420 480 540 600 660 360 420 480 540 600 660 360 420 480 540 600 660
Wavelength,(nm)
Wavelength nm Wavelength, (nm)
Wavelength nm Wavelength (nm)
Wavelength, nm
Figure 2.7. SVD of nanosecond transient spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP;
(E) 3AP and (F) 4AP derivatives in CHCl3.
A) B) C)
0.15 V1 V1
V1
0.15
0.12
0.10
 O. D.
0.10
 O. D.
 O. D.
0.06
0.05
0.05
0.00 0.00 0.00
0 1 2 3 4 0 1 2 3 4 0 1 2 3 4
Time (s Time Time
Time,(s)
s
Time, s ) Time,(s)
s
D) V1 E) V1 F) 0.10
V1
0.09 0.12
0.08
 O. D.
0.09 0.06
0.06
 O. D.
 O. D.
0.06 0.04
0.03
0.03 0.02
0.00 0.00
0.00
0 1 2 3 4 0 1 2 3 4 0 1 2 3 4
Time
Time,(s) Time Time
Time,(s)
s
s Time,(s)
s
Figure 2.8. SVD of nanosecond transient spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP;
(E) 3AP and (F) 4AP derivatives in CHCl3.

component with the right singular vector at the respective transient absorption
spectrum, corresponding to Tn←T1 transition. Right singular vector at 450 nm for 1, 2
and 2’’AP, exhibits triplet lifetime (T) of 4.85, 5.76 and 7.04 s, respectively, while
right singular vector at 490 nm for 2’’ and 3AP decay with a T of 10.13 and 11.8 s,
respectively. A 2.5-fold increase in the T was observed for 4AP in comparison with
1AP, which shows a triplet lifetime of 12.16 s for the observed transient peak at 500
nm. Thus, a linear dependence on the rate of decay of the triplet excited state is
observed on increasing the number of carbonyl substitution in the pyrene unit (Figure
2.9A, Table 2.2). Triplet quantum yield (T) of 14AP derivatives were determined by
using triplet–triplet energy transfer to -carotene with a tris(bipyridyl)ruthenium(II)
complex ([Ru(bpy)3]2+) as a reference[91]. T was determined by initially preparing
optically matched (355 nm) solutions of [Ru(bpy)3]2+ or 14AP derivatives in methanol
and chloroform respectively, and were mixed with a known volume of - carotene
solution. The transient absorbance (A) of the -carotene triplet, which was formed
A) B)
Figure 2.9. Shows A) Variation of triplet lifetime and B) triplet quantum yield of 1-4AP in
CHCl3.
by energy transfer from [Ru(bpy)3]2+ or 14AP triplet to -carotene was monitored at
510 nm. T of AP derivatives are calculated to be 52.30% (1AP), 90.09% (2AP), 96.06%
(2’AP), 94.53% (2’’AP), 96.43% (3AP) and 97.03% (4AP). An remarkable enhancement
in the ΦT of AP derivatives with increase in the number of acetyl group(s) when
compared to P (38.0%)[92] suggest the dominant role of carbonyl group in facilitating
efficient ISC for triplet generation (Figure 2.9B, Table 2.2).
2.3.3. Femtosecond transient studies
fTA measurements were performed on 14AP in chloroform to investigate the
photo-processes that occur in subnano/pico seconds (Figure 2.10). Upon excitation at
400 nm, using 110 fs laser pulse, 14AP exhibits transient absorption band initially
evolved at 534 nm (1AP), 570 nm (2AP), 520 nm (2’AP), 520 nm (2’’AP), 580 nm (3AP)
and 595 nm (4AP). Foggi and co-workers have observed a similar spectral feature in
the transient absorption spectra of P, after 340 nm excitation, populating higher
A) B) 0.44 ps
C) 0.49 ps
0.50 ps
13 ps 12 ps
27 ps 27 ps
35 ps 27 ps
1.2 ns
1.2 ns 1.8 ns
D) E) F)
0.64 ps 0.7 ps 0.94 ps
27 ps
13 ps 27 ps 12 ps 27 ps 11 ps
1.5 ns 1.8 ns
1.5 ns
Figure 2.10. fTA spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP
energy singlet (Sp) state (SnSp transitions, where p > n). The singlet excited state (Sp)
with an absorption maximum at 580 nm undergoes an ultrafast internal conversion
within the singlet manifolds with a rate constant of 150 fs. This result supports the
observed transient peak for 14AP monitored around 534-595 nm which undergoes
ultrafast decay in subpicosecond time scale. It is pertinent to note that while the peak
around 534-595 nm decays, concomitant appearance of another peak at 450 nm (1AP),
450 nm (2AP), 480 nm (2’AP), 480 nm (2’’AP), 490 nm (3AP) and 500 nm (4AP) is
observed within a time scale less than 10 ps (Figure 2.11). The observed peak at 450-
500 nm, then decays within a time delay of 2 ns creating a long-lived absorption band.
SVD followed by global analysis was employed to extract the lifetimes and decay
associated spectra (DAS) from the multidimensional time-resolved absorption data.
Data analysis offered two principle components around 534-595 nm and 450- 500 nm
Figure 2.11. Transient absorption spectra for 4AP as plotted in the early time delay where at
3.5 ps a growth around 500 nm is observed.

respectively (Figure 2.12&2.13; Table 2.4). Two lifetimes are needed to fit the kinetic
profile of the first principle component (V1), whereas V2 decays mono exponentially.
A) B) C)
V1 0.018 V1
0.003
V2 V1 0.012 V2
0.015
V2
0.002 0.012 0.009
 O. D.
 O. D.
 O. D.
0.001 0.009 0.006
0.006 0.003
0.000
0.003
0.000
-0.001 0.000
-0.003
450 500 550 600 -0.003
Wavelength (nm) 450 500 550 600 450 500 550 600
Wavelength (nm) Wavelength (nm)
D) E) F)
V1 0.0175 V1
0.008 0.024 V1
V2 V2 0.0140 V2
0.006 0.018
0.012 0.0105
 O. D.
 O. D.
0.004
 O. D.
0.006 0.0070
0.002
0.000 0.0035
0.000 -0.006 0.0000
-0.002 -0.012 -0.0035
450 500 550 600 450 500 550 600
450 500 550 600
Wavelength (nm)
Figure 2.12. SVD of fTA spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F)
4AP in CHCl3.
A) B) C)
0.4 V1 0.15 V1 V1
0.015
V2 V2 V2
0.10 0.012
0.2
0.009
 O. D.
0.05
 O. D.
 O. D.
0.0 0.006
0.00 0.003
-0.2 -0.05 0.000
-0.003
-0.10
-0.4
0.0 0.2 0.4 0.6 0.8 1.0 1.2 0.0 0.3 0.6 0.9 1.2 1.5 1.8 0.0 0.3 0.6 0.9 1.2 1.5 1.8
Time Time (s)
D) Time (s)
Time, ns E) 0.20 Time,(s)
ns F) Time, ns
V1 V1 V1
0.15
0.075 V2 0.15 V2 V2
0.10
0.10
0.050
0.05
 O. D.
 O. D.
0.05
 O. D.
0.025 0.00
0.00
-0.05 -0.05
0.000
-0.10 -0.10
-0.025 -0.15
0.0 0.3 0.6 0.9 1.2 1.5 1.8 0.0 0.3 0.6 0.9 1.2 1.5 1.8 0.0 0.3 0.6 0.9 1.2 1.5 1.8
Time (s) Time (s) Time (s)
Time, ns Time, ns Time, ns
Figure 2.13. Right singular vectors obtained from global analyses for (A) 1AP; (B) 2AP; (C)
2’AP; (D) 2”AP; (E) 3AP and (F) 4AP in CHCl3.

Table 2.4. Lifetimes of 1-4AP obtained from global analyses of fTA spectra (exc=400 nm).
V1 (ps) V2 (ns)
1 (Sp→Sn)* 2 (Sn→Tm)* (Tm→Tn)*
1 AP 0.54 (76%) 9.08 (24%) 0.12
2 AP 0.70 (65%) 7.45 (35%) 0.27
2’ AP 0.92 (54%) 10.28 (46%) 0.42
2” AP 0.43 (80%) 5.42 (12%) 0.48
3 AP 0.58 (78%) 11.27 (22%) 0.54
4 AP 1.40 (61%) 7.9 (39%) 1.96
*p>n; *m>n
The DAS are shown in Figure 2.12 and the lifetime corresponding to the kinetic
profiles are tabulated in Table 2.4. The short-lifetime component (150 fs) affiliated
with the DAS centered around 534-595 nm attributes to the relaxation pathway from
a higher excited state (Sp) state to a lower singlet excited state (Sn) through internal
conversion (Table 2.4). The second lifetime (2) is assigned to intersystem crossing
(ISC) from the singlet excited state to a receiving triplet state (Tn) (Table 2.4). This
assignment is supported by an isobestic point in the transient absorption spectra of 1-
4AP which suggests the state-to-state relaxation dynamics (Figure 2.11). Crespo-
Hernández and co-workers have observed a similar characteristics in the femtosecond
broadband transient absorption of excited dynamics of
(tricyclohexylphosphine)gold(I) pyrenyl complexes that showed IC in the singlet
manifold followed by 11-100 ps ISC to a receiver triplet state. Consequently, time-
gated emission measurements of 14AP in chloroform at 77 K show phosphorescence
in the spectral 480-650 nm when excited at 350 nm (Figure 2.14A&B Table 2.2). Thus,
A) B)
1.0 Fl
Ph
0.8
0.6
Intensity
0.4
0.2
0.0
400 450 500 550 600 650
Wavelength,(nm)
Wavelength nm
Figure 2.14. (A) Representative phosphorescence spectrum of 4AP in CHCl3 recorded at 77 K
(ex = 380 nm; dotted graph represents the fluorescence spectrum of 4AP) and (B)
phosphorescence decay of 1-4AP derivatives in CHCl3 recorded at 77 K (ex = 380 nm).
photoexcitation of 14AP creates a higher singlet excited state that undergo rapid
intersystem crossing to a triplet state (Tn), effectively competing with the internal
conversion to S1. The long-lived component (3) exhibited a lifetime of 0.12 ns (1AP),
0.27 ns (2AP), 0.42 ns (2’AP) 0.48 ns (2’’AP), 0.54 ns (3AP) and 1.96 ns (4AP) (Table 2.4)
which can be assigned as relaxation within the triplet manifold resulting in the Tn state
(Tn←Tm transition, m > n). The transient peak observed from fTA measurements
around 450-500 nm decays within 2 ns and is in good agreement with the triplet-triplet
(T-T) absorption spectrum obtained from the nanosecond laser experiments (Figure
2.15). Considering the exceedingly high quantum yield (ΦT~100%) for ISC to the
triplet manifold of 14AP in chloroform, suggests plausible small energy gap resulting
in significant spin-orbit coupling between the singlet (ππ*) and triplet (nπ*) excited
states, which explains the ultrafast ISC.

A) B) C)
D) E) F)
Figure 2.15. Overlay of nTA spectra (blue trace) and fTA spectra (red trace) of (A) 1AP; (B)
2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP in CHCl3.
2.3.4. TDDFT calculation and Jablonski diagram
Quantum nuclear dynamics simulations within the linear vibronic coupling
theory were carried out for 2''AP and 4AP to elucidate the experimental Sn←Sp decay.
A vibronic Hamiltonian consisting four low-lying singlet excited states (S4-S1) and
relevant vibrational modes corresponding to intrastate and interstate coupling
parameters has been employed. Although the observed IC decay is difficult to assign
for a particular excited singlet state, it is assumed that the S 4 state is populated upon
electronic excitation in the pump-probe spectroscopy. And, hence the quantum wave
packet dynamics simulations on S4 state are carried out for a meaningful comparison
with the experiment. Figure 2.16A depicts the S4 population decay of 2''AP and 4 AP.
Upon vertical excitation to S4, ~90 % of the population was transferred to lower singlet
states within 20 fs in 2”AP. The decay of S4 is slower in 4 AP compared to 2''AP. For

B)
A)
1.0
2''AP
4AP
Electronic population
0.5 C)
0.0
0 50 100 150 200
Time (fs)
Figure 2.16. A) Decay profile of S4 state of 2’’AP and 4AP; Potential energy cuts along C=O
symmetric stretch vibrational mode of singlet excited states and triplet excited state of B) 2’’AP
and C) 4AP.
further insight on IC and ISC lifetimes and quantum yields, potential energy cuts of
singlet and triplet excited electronic states along the C=O symmetric stretching
vibrations are plotted in Figure 2.16B&C. Based on the near-degenerate energy levels
Figure 2.17. Jablonski diagram depicting the photophysics of acetylpyrene.

of singlet-triplet manifold and quantum dynamics simulations, it is proposed that the
ISC occurring via two pathways, i) Sp→Sn→Tn and ii) Sp→Tm without involvement of
lower singlet excited states, responsible for the observed higher triplet quantum yields
of acetylpyrenes (Figure 2.17).
2.5. Conclusion
In conclusion, we present a comprehensive excited-state dynamical study of
acetylpyrene derivatives using pump-probe transient absorption. Photo-excitation of
acetylpyrene at 400 nm, populates the excited singlet state (Sp) which undergoes rapid
ISC efficiently competing with IC to the lowest excited singlet state (S n). A near unity
ΦT for tetraacetylpyrene (4AP; ΦT~100%) suggest the dominant role of carbonyl group
in facilitating efficient ISC for triplet generation. Ultrafast internal conversion in the
triplet manifold leads to the emitting triplet Tn, which decays radiatively by
phosphorescence with a time scale of 12 s. Our observation will also give further
insight into the utilization of acetylpyrene based molecular systems in molecular
electronics since characterization of triplet excited states is essential for research on
organic photovoltaics and singlet fission.

2.6. Appendix
Experimental section
 Materials and Methods
Pyrene (98%), acetyl chloride (98%) and aluminum chloride (99.99%) were purchased
from Sigma Aldrich and used as such without further purification. Carbon disulfide
used as a solvent for the reaction was dried and distilled by standard procedure. TLC
analysis were performed on precoated aluminum plates of silica gel 60 F254 plates
(0.25 mm, Merck) and developed TLC plates were visualized under short and long
wavelength UV lamps. Flash column chromatography was performed using silica gel
of 200-400 mesh employing a solvent polarity correlated with the TLC mobility
observed for the substance of interest. Yields refer to chromatographically and
spectroscopically homogenous substances.
Melting points (mp) were obtained using a capillary melting point apparatus
and are reported without correction. IR spectra were recorded on a Shimadzu
IRPrestige-21 FT-IR spectrometer as neat KBr pellets for all the derivatives. 1H and 13C
NMR spectra were measured on a 500 MHz and 125 MHz Bruker advanced DPX
spectrometer respectively and 1,1,1,1-tetramethylsilane (TMS) is used as the internal
standard for 1H and 13C NMR measurements. CHN analyses were carried out on an
Elementar vario MICRO cube Elemental Analyzer. All values recorded in elemental
analyses are given in percentages. High Resolution Mass Spectra (HRMS) were
recorded on Agilent 6538 Ultra High Definition (UHD) Accurate-Mass Q-TOF-LC/MS
system using either atmospheric pressure chemical ionization (APCI) or electrospray
ionization (ESI) mode.
Spectral Measurements:
Absorption spectra were recorded on Shimadzu UV-3600 UV-VIS-NIR while
fluorescence and excitation spectra were performed on Horiba Jobin Yvon Fluorolog
spectrometers respectively. The excitation wavelength used is 350 nm unless
otherwise mentioned. Fluorescence lifetime measurements were carried out in an IBH

picosecond single photon counting system. The fluorescence decay profiles were de-
convoluted using IBH data station software version 2.1, and fitted with exponential
decay, minimizing the χ2 values of the fit to 1 ± 0.05. All spectroscopic experiments
were performed by using standard quartz cuvettes of path length 1cm for solution in
dried and distilled solvents. The excitation laser used is 375 nm with a pulse width of
less than 100 ps. 1-4AP derivatives in chloroform were found to have lifetime
significantly shorter than the excitation pulse width. The solution state fluorescence
quantum yields were determined by using optically matched solutions. Quinine
sulfate dissolved in 0.5 M H2SO4 (Φf = 0.546) is used as the standard for 1-4AP
derivatives.
Nanosecond transient absorption measurements. Nanosecond laser flash photolysis
experiments of the argon purged solutions were carried out in an Applied
Photophysics Model LKS-60 laser kinetic spectrometer using the third harmonic (355
nm, pulse duration ≈10 ns) of a Quanta Ray INDI-40-10 series pulsed Nd:YAG laser
as the excitation source. Triplet states of 1-4AP in CHCl3 were confirmed performing
the experiments with oxygen purged solutions.
Femtosecond pump-probe transient absorption technique. Spectra-physics Tsunami
Oscillator (80 MHz, 800 nm) was used as seed for a Spectra-Physics Spitfire
Regenerative amplifier (1 KHz, 4 mJ). A fraction of the amplified output was used to
generate 400 nm pump pulse. Residual 800 nm pulse was sent through a delay line
inside an Excipro pump-probe spectrometer from CDP Systems. A rotating CaF2 plate
(2 mm thickness) was used to generate continuum of white light from the delayed 800
nm pulses. The continuum of white light was split into two and the streams were used
as probe and pump pulses. Transient absorption spectra were recorded using a dual
diode array detector with a 200 nm detection window with an optical delay of 1.6 fs.
Near infrared measurements were performed using a multichannel infrared detector
that scans from 900 to 1600 nm. Sample solutions were prepared in a rotating sample
cell with 4 mm path length. IRF was determined by solvent (10% benzene in methanol)
two photon absorption and was found to be approximately 110 fs at about 530 nm.
Energy per pulse incident on the sample is attenuated employing 80% neutral density
filter when required.
fTA measurements of 1-4AP derivatives in CHCl3 were carried out by exciting the
respective sample at 400 nm, 200 nJ, ~110 fs pulses, allowing excitation of pyrene unit.
Cyclic Voltammetry (CV): Electrochemical measurements were performed on a BASi
(Bioanalytical Systems, Inc.) C-3 cell stand controlled by Epsilon electrochemical
workstation. A three electrode system is then constructed constituting a glassy carbon
as the working electrode, a platinum-wire as the counter electrode, and an Ag/Ag+ (3
M NaCl) as the reference electrode. The electrochemical measurements were
conducted under nitrogen atmosphere (5 psi, 10 minutes) in a deoxygenated
anhydrous acetonitrile of tetra-n-butylammonium hexafluorophosphate (supporting
electrolyte, 0.1 M) for AP derivatves, in CHCl3 with a scan rate of 50–100 mVs−1.
Calibration of the instrument was performed using the ferrocene/ferrocenium (Fc/Fc+)
redox couple as an internal standard and measured under same condition before and
after the measurement of samples. The energy level of Fc/Fc+ was assumed to be -4.8
eV with respect to vacuum. The half-wave potential of Fc/Fc+ was estimated to be 0.5
V with reference to the Ag/Ag+ electrode.
HOMO and LUMO energy levels were calculated from the following equations:
onset
EHOMO = −(Eox + 4.8) eV and (1)
onset
ELUMO = −(Ered + 4.8) eV (2)
onset onset
respectively, where Eox and Ered are the onset oxidation and reduction potentials
relative to the Ag/Ag+ reference electrode.
The electrochemical energy gap (Eg) is estimated as follows:

Eg = (ELUMO − EHOMO ) eV (3)
where ELUMO and EHOMO are the corresponding to HOMO and LUMO energy levels
calculated after converting the values in Ag/Ag+ with respect to the standard calomel
electrode (SCE) convention.
Determination of fluorescence quantum yield and radiative and non-radiative rate
constants: Solution state fluorescence quantum yields of AP derivatives were

calculated by relative quantum yield method as follows,

I OD n
⏀s = ⏀ref (I s )( ODref )(n s )2 (4)
ref s ref
wherein, ⏀s and ⏀ref are the quantum yields of sample and reference respectively,
Is and Iref are the area under the emission spectrum for sample and reference
respectively. ODs and ODref are the absorbances of sample and reference respectively
at the excitation wavelength. ns and nref are the refractive index of the solvent in
which sample and reference are taken.
Radiative (k r ) and non-radiative (k nr ) rate constants from the singlet excited states are
calculated from the fluorescence quantum yields, ⏀f.

kr
⏀f = k (5)
r +knr
The rate constants k r and k nr can be evaluated by measuring fluorescence lifetimes (f)
from TCSPC measurements. The following equations depict relation between⏀f , f,
k r and k nr .
⏀f
kr = and (6)
τf
1−⏀f
k nr = (7)
τf
a change in ⏀f could be attributed to the changes in either k r /k nr . The enhancement
in the quantum yield (⏀f ) with increased solvent polarity is due to the stabilization of
the excited states by virtue of interaction with the solvent dipoles and decrease in the
non-radiative (k nr ) rate constant.
X-ray Crystallography
X-ray Crystallography: High-quality specimens of appropriate dimensions were
selected for the Xray diffraction experiments. Crystallographic data collected are
presented in the supplementary information. Single crystals were mounted using oil
(Infineum V8512) on a glass fibre. All measurements were made on a CCD area
detector with graphite monochromated Mo Kα radiation. The data was collected
using Bruker APEXII detector and processed using APEX2 from Bruker. All structures
were solved by direct methods and expanded using Fourier techniques. The non-
hydrogen atoms were refined anisotropically. Hydrogen atoms were included in

idealized positions, but not refined. Their positions were constrained relative to their
parent atom using the appropriate HFIX command in SHELXL-97. The full validation
of CIFs and structure factors of 1-4AP derivatives were performed using the CheckCIF
utility and found to be free of major alert level. 3D structure visualization and the
exploration of the crystal packing of 14AP were carried out using Mercury 3.1.
Computational Methods
Geometry optimization and single point energy calculations for 1-4AP performed at
B3LYP/6-311G**++ level of theory using the crystal structure data, for Frontier
molecular orbital (FMO) analyses. Energy gap is determined as the difference between
energies of LUMO and HOMO as described in equation 3. Energy level diagram is
plotted using the energies obtained from FMO analyses. All computations were
performed with the Gaussian 09 program suite.
Synthesis Details
Scheme 2.1. Shows the synthesis of acetylpyrene (1-4AP) derivatives.
Preparation of acetylpyrene (1-4AP) derivatives: Pyrene dissolved in CS2 (yellow
solution) was maintained at ambient temperature and subsequently anhydrous AlCl3
was added. Acetyl chloride was then slowly syringed to the suspension.
Subsequently, hydrogen chloride was liberated. After 3 hrs the mixture was added
slowly to a vigorously stirred mixture of ice and concentrated HCl. The resulting
suspension was filtered and vacuum dried and purified through column
chromatography (silica gel) to give acetylpyrene (1-4AP) derivatives.
1AP (yield= 5.1%). M.p. 90.4-91.8°C. 1H NMR [500 MHz, C2D2Cl4, δ]: 9.09 (d, J= 9.35
Hz, 1H), 8.43 (d, J = 8.05 Hz, 1H), 8.33 (d, J = 2.9 Hz, 1H), 8.32 (d, J = 2.9 Hz, 1H), 8.29
(d, J = 9.4 Hz, 1H), 8.24 (d, J = 1.35 Hz, 1H), 8.22 (s, 1H), 8.13 (m, 2H), 2.96 (s, 3H). 13C
NMR [125 MHz, C2D2Cl4, δ]: 202.57, 134.08, 131.96, 131.11, 130.47, 129.91, 129.86,
129.40, 127.37, 127.31, 126.72, 126.67, 126.34, 125.06, 124.97, 124.30, 124.26, 30.74. IR
(KBr, cm-1): 3041, 1675, 1249. Elemental analysis: calcd. value for C18H12O: 88.50% C,
4.95% H; found: 88.78% C, 4.88% H. HRMS (EI) m/z calculated for C18H12O [M]+:
244.0888, found: 244.0872.
2AP (yield= 9.4%). M.p. 179.0-181.1°C. 1H NMR [500 MHz, DMSO (d6), δ]: 8.87 (s, 1H),
8.78 (d, J = 9.30 Hz, 2H), 8.38 (d, J =7.65 Hz, 2H), 8.35 (d, J = 9.35 Hz, 2H), 8.13 (t, J =
7.60 Hz, 1H), 2.88 (s, 6H). 13C NMR [125 MHz, DMSO (d6), δ]: 201.94, 131.41, 131.21,
130.37, 129.87, 128.03, 127.43, 127.20, 124.39, 124.18, 123.19, 30.71. IR (KBr, cm-1): 3048,
1681, 1249. Elemental analysis: calcd. value for C20H14O2: 83.90% C, 4.93% H; found:
84.07% C, 4.93% H. HRMS (EI) m/z calculated for C20H14O2 [M]+: 286.0994, found:
286.0991.
2’AP (yield= 9.6%) M.p. 205.7-206.9°C. 1H NMR [500 MHz, DMSO (d6), δ]: 8.86 (d, J =
9.35 Hz, 2H), 8.55 (d, J = 8.05 Hz, 2H), 8.35 (d, J = 8.05 Hz, 2H), 8.28 (d, J = 9.40 Hz, 2H),
2.83 (s, 6H). 13C NMR [125 MHz, DMSO (d6), δ]: 202.20, 133.33, 132.31, 129.07, 128.20,
127.73, 126.39, 125.35, 123.73, 30.64. IR (KBr, cm-1): 3028, 1676, 1251. Elemental analysis:
calcd. value for C20H14O2: 83.90% C, 4.93% H; found: 83.96% C, 4.90 % H. HRMS (EI)
m/z calculated for C20H14O2 [M]+: 286.0994, found: 286.0986.
2”AP (yield= 37.5%) M.p. 161.6-163°C. 1H NMR [500 MHz, DMSO (d6), δ]: 8.87 (s, 2H),
8.55 (d, J = 8.0 Hz, 2H), 8.37 (d, J = 8.0 Hz, 2H), 8.27 (s, 2H), 2.82 (s, 6H). 13C NMR [125
MHz, DMSO (d6), δ]: 202.02, 133.21, 132.81, 129.14, 127.83, 127.43, 126.40, 125.78,
123.75, 30.58. IR (KBr, cm-1) 3000, 1659, 1231. Elemental analysis: calcd. value for
C20H14O2: 83.90% C, 4.93% H; found: 83.96% C, 4.89% H. HRMS (EI) m/z calculated for
C20H14O2 [M]+: 286.0994, found: 286.0981.
3AP (yield= 18.9%) M.p. 178.8-179.3°C. 1H NMR [500 MHz, CDCl3, δ]:9.13 (d, J = 9.5
Hz, 1H), 9.02 (d, J = 9.0 Hz, 1H), 9.0 (d, J = 9.5 Hz, 1H), 8.70 (s, 1H), 8.47 (d, J = 8.0 Hz,
1H), 8.34 (d, J = 8.0 Hz, 1H), 8.29 (d, J = 9.5 Hz, 1H), 2.97 (s, 6H), 2.95 (s, 3H). 13C NMR
[125 MHz, CDCl3, δ]: 201.72, 201.19, 201.15, 133.87,132.46, 131.96, 131.91, 131.18, 130.66,
130.32, 128.51, 128.09, 127.66, 127.31, 126.17, 126.08, 126.04, 124.67, 123.90, 30.52, 30.51,
30.46. IR (KBr, cm-1): 3020, 1664, 1255. Elemental analysis: calcd. value for C22H16O3:
80.47% C, 4.91% H; found: 80.63% C, 4.87% H. HRMS (EI) m/z calculated for C22H16O3
[M]+: 328.1099, found: 328.1086.
4AP (yield= 4.6%) M.p. 295.6-297.0°C. 1H NMR [500 MHz, C2D2Cl4, δ]: 9.04 (s, 4H), 8.70
(s, 2H), 2.99 (s, 12H). 13C NMR [125 MHz, C2D2Cl4, δ]: 201.80, 134.01, 133.96, 130.47,
128.21, 127.25, 125.25, 30.97. IR (KBr, cm-1): 3004, 1685, 1270. Elemental analysis: calcd.
value for C24H18O4: 77.82% C, 4.90% H; found: 77.61% C, 4.85% H. HRMS (EI) m/z
calculated for C24H18O4 [M]+: 370.1205, found: 370.1210.

Chapter 3
Engineering the solid-state packing of carbonylpyrenes via C–
HH–C, C–HO and – interactions for tuning opto-
physical properties
Abstract
Molecular crystal engineering of polyaromatic hydrocarbons to yield 1–2D lamellar
arrangement demonstrated a pivotal role in photonic and semiconductor device applications.
In this report, we modulated the extent of – overlap between vicinal pyrene units through
successive acylation. Quantum theory of atoms in molecules (QTAIM) and Hirshfeld surface
analyses were employed to understand the close packing interactions which indicates an
increase in  interactions and a concomitant decrease in the  interactions with an
increase in the number of acetyl groups per pyrene unit. A combination of C–HH–C, C–
HO and  interactions facilitate the transformation of sandwich herringbone packing of
P to the herringbone arrangement in 1 and 2’AP, the brickwork arrangement in 2 and 2’’AP
and columnar stacks in 3–4AP. A systematic decrease in the interplanar angle between the
vicinal pyrene units could be attributed to the dramatic shift in the emission spectra (ca. 42–
174 nm) of crystalline 1–4AP when compared to pyrene. J-like aggregation and/or aggregation
induced emission (AIE) in the crystal packing of 1–4AP corroborates the moderately emissive
blue–green–orange crystals.
While in another context, the extent of orbital overlap (π–π) between vicinal pyrene units
in crystalline 1–4BP was regulated by exploiting the steric hindrance offered via successive
benzoylation. Steric hindrance due to incremental benzoyl groups causes a systematic
reduction in the orbital overlap (π–π) between vicinal pyrene units affording green-yellow-
orange solid-state emitters. Crystallization induced emission could arise from: i) electronic
(dipolar/excitonic) interactions, ii) arrested bond rotations, and/or iii) lack of solvation in
crystalline 1–4BP (ΦFl ∼ 2–26%) when compared to that in solution (ΦFl ≤ 1%).
Acylation of pyrene Benzoylation of pyrene
P 1AP 2’AP 2AP 2’’AP 3AP 4AP

Design & Synthesis
Future Applications
1.0 P
Fluorescence Intensity (a. u.)
1AP
2AP
2'AP
2"AP
3AP
4AP
0.5
0.0
400 500 600
Wavelength (nm)
1) Rajagopal, S. K.; Philip, A. M.; Nagarajan, K.; Hariharan, M. Chem. Commun. 2014, 50, 8644-
8647. 2) Rajagopal, S. K.;Reddy, V. S. Hariharan, M. CrystEngComm 2016, 18, 5089-5094.
Chapter 3-Engineering the solid-state packing of carbonylpyrene via C-HH-C, C-HO and - interactions for 82
tuning opto-physical properties
3.1. Introduction
Molecular crystal engineering[93] of polyaromatic hydrocarbons to yield 1–2D
lamellar arrangement demonstrated a pivotal role in photonic[94-96] and
semiconductor device applications[97-100]. Extended orbital overlap through
columnar stacks compared to a herringbone arrangement of arenes proved to be
vital[101-103]. Recent efforts in transforming the herringbone to the columnar
arrangement of arenes through various methods such as chemical modifications[104],
co-[105, 106] and solvent-crystallization[107], heat-mode[108], mechanical
stimulation[109, 110] and solid seeding[111] have proven to be effective. Achieving a
diverse degree of orbital overlap between the neighboring units in the crystalline state
is still a challenging task. Monitoring the effect of subtle orientation differences and
thereby the orbital overlap between the neighboring units in arenes is even more
challenging. The extent of orbital overlap through  interactions between the vicinal
arenes could be reflected in the optical properties of the crystals[23]. Extremely high
sensitivity of pyrene fluorescence towards environmental effects can amplify the
consequence of orientation factor/orbital overlap between the adjacent units[112].
Our ongoing interest to regulate the arene–arene interactions in fluorescent
crystals[113, 114], vesicular gels[115] and thin films prompted us to explore the
correlation between optical properties vs. peripheral substitution of pyrene. We
employed a simple and convenient Friedel–Crafts reaction, invented 137 years
ago[116], to increase the number of carbonyl groups in pyrene. Carbonyl conjugated

arenes in solution exhibit diverse excited state processes[82] depending on the
adjacent functionality such as (i) low fluorescent (f  0.002) aryl aldehydes/ketones
dominated by intersystem crossing (ISC); (ii) moderate fluorescent secondary/tertiary
carboxamides[117] dominated by internal conversion and (iii) high fluorescent aryl
acids/esters[118] dominated by radiative processes. Extremely low f in solution
hampered the efforts to explore the optical properties of aryl ketones/aldehydes in the
crystalline state though a plethora of pyrene derivatives have been explored for
optoelectronic applications[5, 119].
Furthermore, heteropolar C–HH–C interactions are rarely found to be an
integral force in organic crystals when compared to C–HO[120], C–H,
homopolar C–HH–C[122] interactions, etc. Heteropolar C–HH–C interactions
could arise from the dipolar/quadrupolar nature of sp2 C–H bond that could induce a
dipole on the vicinal sp3 C–H unit. Highly electronegative substituents/groups
adjacent, either geminal or vicinal, to a sp2 C–H unit may polarize the bond allowing
for extended interactions[123]. We herein report for the first time a systematic control
on the organization of adjacent pyrene units through the progressive addition of
acetyl groups that transform the sandwich herringbone structure of pyrene to a
columnar arrangement in tri/tetraacetylpyrene. Distinct packing arrangements,
through C–HH–C, C–HO and – interactions, in acetylpyrene derivatives offer
diverse solid-state colouring and fluorescent properties.
Crystalline pyrene based blue organic light emitting devices (OLED) suffer from
strong excimer contributions[124]. Disruption of nearest neighbour interactions in

crystalline pyrene is expected to enhance the performance of OLEDs[125]. A variety
of chemical[126-130] and physical approaches[98, 107] have been utilized to regulate
pyrene–pyrene interactions. Efforts to tune the interchromophoric interactions in
molecular crystals using π–π[85, 115], C–Hπ[113, 131], C–HO[132] and C–HH–
C[133] contacts for favourable photophysical properties allowed us to employ the
combination of steric and conjugation effects of benzoyl units of pyrene based
systems. The significant dimension of the benzoyl unit (105.2 Å3)[134] as compared to
pyrene (237.5 Å3) could potentially perturb strong π–π interactions (−13.8 kcal mol−1)
[135] between the nearest pyrene units (center-to-center distance of 3.53 Å) (Figure
3.1).
A)
B)
Figure 3.1. Volume calculated for (A) pyrene and (B) benzoyl unit in 1BP from Crystal
Explorer 3.0.
3.2.1. Synthesis, crystallization and thermal analysis
Adding a stoichiometric quantity of acetyl chloride to a solution of pyrene and
AlCl3 in carbon disulfide (CS2) at ambient temperature rendered the desired acetyl
derivatives (1–4AP) with moderate yield (Figure 3.2, Row I)[13]. Compounds (1, 2, 2’,
2’’, 3AP) were crystallized by varying the acetone:hexane composition, whereas 4AP
was obtained by temperature gradient cooling in chloroform. Acetyl derivatives (1, 2’,
2’’, 3, 4AP) yielded solvent free monoclinic crystal system except for 2AP which
exhibits a solvent free orthorhombic crystal system (Figure 3.2, Row II; Table 3.1).
Differential scanning calorimetric (DSC) analysis of 1-acetylpyrene (1AP) exhibited a
sharp melting transition (Tm) at 90.4 1C (Figure 3.3A). A significant decrease (ca. 63
P 1AP 2AP 2’AP 2”AP 3AP 4AP

II
III
IV
Figure 3.2. Row I: molecular structure of 1–4AP; Row II: corresponding single crystal X-ray
structure. Photographic image of the crystals Row III: in daylight; and Row IV: under UV
illumination. X-ray structure of P is taken from the literature[136].

Chapter 3-Engineering the solid-state packing of carbonylpyrene via C-HH-C, C-HO and - interactions for tuning opto-physical properties 86
Table 3.1. Shows crystallographic data and refinement parameters for crystalline 1-4AP derivatives.

formula C18H12O C20H14O2 C20H14O2 C20H14O2 C22H16O3 C24H18O4
formula wt 244.28 286.31 286.31 286.31 328.35 370.38
colour, shape Pale Yellow Yellow Yellow Yellow Yellow Orange
dimens, mm 0.20x0.15x0.10 0.20x0.15x0.10 0.25x0.20x0.15 0.20x0.15x0.10 0.20x0.15x0.10 0.20x0.10x0.10
crystal system Monoclinic Orthorhombic Monoclinic Monoclinic Monoclinic Monoclinic
space group, Z Cc Pnma P2(1)/n P2(1)/c P2(1)/c C2
a, Å 34.4472 7.3519 9.243 8.1941 11.0402 20.1864
b, Å 7.3598 16.6654 7.463 23.0417 20.0564 39.6060
c, Å 9.8621 11.3344 10.095 7.4020 7.2682 7.0261
α, deg 90.00 90.00 90.000 90.00 90 90.00
β, deg 98.492 90.00 98.880 93.824 96.682 109.988
γ, deg 90.00 90.00 90.000 90.00 90 90.00
3
V, Å 2472.87 1388.72 688.0 1394.43 1598.44 5279.0
temp, K 296 296 296 296 296 293
-3
dcalcd, g/cm 1.312 1.369 1.382 1.364 1.364 1.398
no. of reflections collected 9183 5744 4832 10022 12353 15979
no. of unique reflections 3756 1269 1200 2408 2825 8235
2max, deg 50 50 50 50 50 50
no. of parameters 343 106 128 201 226 1023
R1, wR2
0.0418, 0.1111 0.0427, 0.1126 0.0416, 0.1148 0.0764, 0.1157 0.0612, 0.1756 0.0893, 0.2275
(I > 2(I))
R1, wR2
0.0489, 0.1268 0.0601, 0.1277 0.0562, 0.1229 0.1201, 0.1314 0.1276, 0.2316 0.1412, 0.2631
(all data)
goodness of fit 1.053 1.036 1.069 1.068 1.061 1.069
CCDC number CCDC 984436 CCDC 984437 CCDC 984438 CCDC 984439 CCDC 984440 CCDC 984441
B)
A)
C)
Figure 3.3. Shows (A) DSC melting temperature (Tm); (B) near-linear increment in the
melting temperature (Tm) and (C) linear increment in the ΔH values of crystalline 1-4AP
derivatives.
C) in the Tm of 1AP when compared to the Tm of the model compound pyrene (P)[137]
is indicative of attenuation in the ordered arrangement of the crystalline 1AP.
However, further increase in the number of acetyl groups in the pyrene core resulted
Table 3.2. Shows melting temperature (Tm) and change in enthalpy (ΔH) values for crystalline
1-4AP derivatives.
aTm (°C) b ΔH (kJ/mole)
1AP 90.4 25.24
2”AP 161.7 29.45
2AP 179.0 32.41
3AP 178.8 36.86
2’AP 205.7 42.00
4AP 295.6 47.96

a Melting temperature; bChange in enthalpy during melting
in a near-linear increase (Figure 3.3B) in the Tm having a maximum of 295.6 C as in
the symmetric 4AP derivative. A similar trend was observed for the change in
enthalpy during the melting process for 1–4AP (Figure 3.3C and Table 3.2).
2.3.2. QTAIM and Hirshfeld analyses
Qualitative analyses of the single crystal X-ray structure of 1–4AP indicate intra-
and intermolecular distances between the methyl and aryl hydrogens in the range of
2.098–2.4 Å (Tables 3.3 and Figure 3.4). Distances appearing at less than the double of
van der Waal’s radius of hydrogen atom (2.4 Å) could indicate the existence of
dihydrogen (HH) bonding[138]. Quantum theory of atoms in molecules analyses
(QTAIM)[139, 140] of the crystalline 1–4AP offered no characteristics supporting the
intramolecular dihydrogen interactions at distances less than 2.4 Å. Intermolecular C–
HH–C interactions in crystalline 2, 3 and 4AP (Figure 3.4) are exemplified through
the values of electron density at the (3, -1) bond critical point (BCP; b(r)), its Laplacian
Table 3.3. Shows intramolecular (CH3) HH (aryl) (Å) distance (d) in crystalline 1-4AP
derivatives that is less than the sum of van der Waals radii of two hydrogen atoms (2.4 Å).
H18c H18a H20a H20c

C18
H2
Interaction d, (Å)
H20b C20
H18b 1AP H18aH2 2.183
C17 C19
O1 H18aH2 2.098
C2
O2 2AP
C1 C3
H20aH2 2.098
C11 C13
H18aH2 2.350
H10 C12 2’AP
H4 H22aH7 2.350
C10 C4
H18aH2 2.315
C9 2”AP
C5 H24aH7 2.356
H9 H5
C14 C15
C16 H18aH2 2.186
C6
3AP H20aH2 2.146
C8 C7
O4 C23 H22aH7 2.144
C21 O3
H18aH2 2.078
C24 H24a H7 H22c H20aH2 2.186
H24c H22a C22 4AP
H24b H22aH7 2.055
H22b
H24aH7 2.139
(b(r)), the interaction distance (d) as indicated in Table 3.4, a bond and virial path
in the potential energy density map. A closed-shell intermolecular C– HH–C
interaction possessing considerable bond path between a pair of similar hydrogens
Table 3.4. Shows calculated topological properties of the electron density for the intra- and
intermolecular interaction in 2, 3 and 4AP derivatives.
 (r),
b b cb(r), dDE
Description Interaction ad, (Å)
eÅ-3 eÅ-5 (kJ mol-1)
H18cH’18c 2.230 0.036 0.520 3.46
O1H10 2.325 0.093 1.354
2AP O2H4 2.335 0.093 1.354
O’1H’10 2.335 0.093 1.356
O’2H’4 2.335 0.093 1.355
H20cH’8 2.246 0.041 0.471 4.29
H20cH’9 2.579* 0.019 0.249 1.87
O1H10 2.185 0.127 1.892
O2H4 2.199 0.123 1.838
3AP O3H5 2.298 0.101 1.474
O’2H’4 2.199 0.123 1.836
O2H’9 3.242 0.013 0.182
O’3H’5 2.299 0.101 1.473
O’1H’10 2.185 0.127 1.892
H’18cH”22c 2.239 0.040 0.514 4.32
H’4H18a 2.394 0.034 0.450 3.50
H’5H18c 2.577* 0.023 0.300 2.29
O2H4 2.186 0.128 1.897
O4H9 2.210 0.121 1.785
O1H10 2.322 0.096 1.411
O3H5 2.354 0.091 1.314
O’1H”22c 2.490 0.062 0.708
O”3H’18c 2.490 0.062 0.708
4AP
O’3H’5 2.186 0.127 1.897
O’1H’10 2.210 0.121 1.786
O’4H’9 2.322 0.095 1.412
O’2H’4 2.354 0.091 1.313
O”4H9 2.354 0.091 1.312
O”3H”5 2.210 0.120 1.785
O’2H20b 3.309 0.013 0.175
O”1H”10 2.186 0.127 1.898
O”2H”4 2.322 0.096 1.411
ad = distance bb(r) = electron density at the BCP. cb(r) = Laplacian of bb(r). dDE = dissociation
energy. *Though HH distance is >2.4 Å, QTAIM exhibited electron density at (3, -1) BCP.
(CH3) is seen in 2AP (Figure 3.4A). Non polar C–HH–C interaction evaluated
accumulation of electron density, b(r), 0.036 eÅ-3 and the positive value of the
Laplacian at the BCP (0.52 eÅ-5), to form extended chain-like C–HH–C contacts
along the b-axis in 2AP. Derivatives 1, 2’ and 2’’AP lack intermolecular C– HH–C
interaction as confirmed through QTAIM calculations. Similar electronegativity
differences between involved sp3 C–H bonds could only arise from electrically neutral
hydrogens in the vicinity. The influence of the adjacent carbonyl group may impart
repulsive C–HH–C interactions from the first order electrostatic contribution. C–
HH–C contacts could be due to second-order mutual polarization of distorted
charge clouds of the C–H bonds due to the vicinal carbonyl group. Carbonyl groups
A) B)
C)
Figure 3.4. Shows QTAIM electron density map of (A) 2AP; (B) 3AP and (C) 4AP, arrows
indicate the existence of intermolecular C–HH–C contacts.

adjacent to the interacting sp3 methyl groups could make the C–H bonds both
polarizable and polarizing with respect to each other, as observed for B– H bonds[141].
3AP exhibits (CH3)HH(aryl) interactions whereas 4AP shows a bond path for
(CH3)HH(CH3) and (CH3)HH(aryl) interactions (Figure 3.4B&C). QTAIM
calculations also confirmed the existence of C–HO and C–HC interactions in the
derivatives 2–4AP, apart from the C–HH–C contacts (Table 3.4).
Hirshfeld surface analyses[134] of 1–4AP (Figure 3.5 and Table 3.5) exhibit
systematic trends in the weak interactions with an increase in the number of
A) C) D)
2.4
2.2
2.0
1.8
1.6
1.4
1.2
1.0
0.8
0.6
0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4
B) E)
edge-face face-face
2.4 - stack - stack 50
% C---H interaction
% C---C interaction
2.2 15
2.0 40
1.8
1.6 10 30
1.4
1.2 20
1.0
5
0.8 10
0.6
0
0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 2.2 2.4 1AP 2'AP 2''AP 2AP 3AP 4AP
Figure 3.5. Hirshfeld 2D fingerprint plot of 4AP with the region of the plots corresponding to
(A) CC and (B) HH interactions; Hirshfeld surface of 4AP mapped with dnorm depicting;
(C) CC and (D) HH interactions and (E) percentage contribution of edge-to-face (CH)
and face-to-face (CC) interactions in 1–4AP.

Table 3.5. Percentage of intermolecular contacts of a molecule in crystalline 1-4AP.
Interaction 1AP 2AP 2’AP 2”AP 3AP 4AP
HH % 38.8 42.3 40.8 42.7 45.8 45.3
CH % 46.9 26.4 35.9 27.0 13.2 7.4
OH % 11.3 19.0 15.0 18.5 21.4 25.8
CC % 2.4 10.3 3 9.9 14.8 16.1
CO % 0.5 1.9 5.3 1.8 4.2 4.7

atotal percentage of intermolecular contacts ca. 99.9% (1AP), 99.9% (2AP), 100% (2’AP),
99.9% (2”AP), 99.4% (3AP), 99.3% (4AP).
substituted acetyl groups per pyrene unit as the following (i) decrease in the CH
contacts that corresponds to  (edge-to-face) interactions; (ii) increase in the
contacts that corresponds to  (face-to-face) interactions; (iii) increase in the OH
contacts that corresponds to C–HO interactions; (iv) increase in the HH contacts
that corresponds to dihydrogen interactions and (v) increase in the OC contacts that
corresponds to dipolar interactions between the carbonyl groups.
2.3.3. Crystal structure analyses of 1-4AP
Concurrence of such weak intermolecular interactions dictates the molecular
packing that results in ideal columnar 2D stacks in 4AP having  = 0.46 (Figure 3.6). A
value of  = 19.5 in 1AP indicates the formation of a herringbone structure in the
crystalline lattice when compared to the sandwich herringbone structure in the P ( =
3.4). Efficient reduction in the  value from 1–4AP is a consequence of simultaneous
(i) decrease in the percentage of CH contacts ( stacking) from 46.9% (1AP) to
7.4% (4AP) and (ii) increase in the CC contacts ( stacking) from 2.4% (1AP) to
P 1AP 2AP 2’AP

Sandwich herringbone Herringbone Lamellar 2-D π-π stack/ Herringbone
.40 9.54 motif / Brickwork .56 .97
2’’AP 3AP 4AP

Lamellar 2-D π-π stack/ Columnar 2-D π-π stack/ Columnar 2-D π-π stack/
motif / Brickwork (.7 motif (0.89 motif (0.46
Figure 3.6. Close packing arrangement in 1–4AP indicating the values of
[(%CH)/(%CC)][30]. Herringbone (> 4.5), sandwich herringbone (3.2 < < 4.0), 
(1.2 < < 2.7),  (0.46 < < 1.0).
16.1% (4AP). With increase in the number of acetyl groups in pyrene core, crystal
packing of 1–4AP shows distinct patterns through a gradual decrease in the
interplanar angle between adjacent pyrene units (y = 48.4 for 1AP and y = 0 for 4AP;
Figure 3.7A and B and Table 3.6). Decrease in the interplanar angle was accompanied
A) B)
1AP
2’AP
2’’AP
2AP
3AP
4AP
Figure 3.7. Shows (A) the gradual decrease in the interplanar angle between the nearest
molecules and (B) the decreasing angle and the consequent increase in stacking of the pyrene
units in the crystalline 1-4AP.

Table 3.6. Interplanar angle between nearest pyrene molecules in crystalline 1-4AP.
Angle, deg
1AP 48.4, 50.5, 51.1
2AP 11.1
2’AP 30.2
2’’AP 14.5
3AP 7.2
4AP 0, 3.9, 5.9
by transformation of the herringbone structure of 1AP to the columnar structure of
4AP. 2’AP shows herringbone packing without – overlap between adjacent pyrene
units while the crystal structure of 2, 2’’AP shows a lamellar motif with 2D –
stacking (brickwork/-motif). The torsional angles between the planes of adjacent
pyrene units in 2, 2’’AP were found to be 0 and 1, respectively (Figure 3.8 and 3.9).
3AP shows columnar stacks with extended 2D – stacking (-motif), consistent with
4AP. While 3AP exhibited a torsional angle of 67.8 between the planes of adjacent
pyrene units, a near-orthogonal (80.4) arrangement of pyrene units was observed for
4AP, consistent with the 1,3,6,8-tetraphenylpyrene derivatives reported by Geerts,
Bredas and co-workers[142]. We observed a – stacking distance of 3.4–3.5 Å in 4AP
when compared to 4.8 Å in 1,3,6,8-tetrakis(4-methoxyphenyl)-pyrene reported earlier.
By virtue of the smaller size of the acetyl vs. phenyl substituents, we observed a
shorter  stacking distance in 4AP. In 2AP, carbonyl oxygen interacts with the aryl
hydrogen (C–HO; Figure 3.10) forming a zig-zag arrangement along the b-axis (out-
of-plane; 1D), while 2’AP favors a linear arrangement along the c-axis possessing C–
HO interactions. An interplanar angle of 14.51 between the pyrene units in 2’’AP
A) B)
68.1
C) D)
23.4
E) F)
67.8
80.4
Figure 3.8. Shows the torsional angle between adjacent pyrene units in crystal packing of (A)
1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP.
arises from C–HO contacts. Extended C–HO interactions in 3–4AP across the ab-
plane promotes a sheet-like arrangement of pyrene units (Figure 3.10) in combination
with interplanar C–HO interactions that support the pyrene (-structure) stacks
along the c-axis. In addition to C–HO interactions, we observed C–HH–C contacts

(3.46–4.32 kJ mol-1; Table 3.4) in crystalline 2–4AP. C–HH–C contacts in 2AP (b-axis;
in-plane; 1D) and 3AP (a-axis; in-plane; 1D) promote a linear arrangement of the
A)a) b)
B)
c)
C) d)
D)
F)
f)
e)
E)
Figure 3.9. Shows the aerial overlap between adjacent pyrene units in close packing of (A)
1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E) 3AP and (F) 4AP.
pyrene units. In 4AP, C–HO interactions promote stacks along the c-axis which is
reinforced by C–HH–C contacts across the ab-plane.
A)
B)
C)
D)
E)
Figure 3.10. Shows the C–HO interactions in the crystal packing of (A) 2AP; (B) 2’AP;
(C) 2”AP; (D) 3AP and (E) 4AP.

2.3.4. Steady-state absorption and emission measurements
We performed steady-state and time-resolved photophysical measurements to
correlate the extent of overlap between adjacent pyrene units vs. colour properties in
crystalline 1–4AP. Experiments were also carried out in dilute solutions of chloroform
to understand the photophysical properties of 1–4AP. Increasing the number of acetyl
groups resulted in progressive red-shift in the UV-Vis absorption maximum of 1–4AP
in chloroform, for example 22 nm (1AP) and 70 nm (4AP), when compared to P (Figure
2.4A and Table 3.7). Upon excitation at 350 nm, the emission maximum of 1–4AP in
chloroform exhibited a similar trend indicating the role of extended conjugation
Figure 3.11. Shows fluorescence decay profile of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP; (E)
3AP and (F) 4AP in CHCl3 solution on exciting at 375 nm and collected at different
wavelengths.
arising from carbonyl group(s) in the electronic transitions in the pyrene unit (Figure
2.4B and Table 3.7). We observed a significant decrease in the fluorescence quantum
yield of 1–4AP (f ≥ 0.9%, Table 3.7) in chloroform when compared to P (f = 75%)[89].
Observed low f of 1–4AP in chloroform could be attributed to alternate excited state
decay pathways (knr  kISC >>> kr) due to the incorporation of acetyl group(s)[82].
Picosecond time-resolved fluorescence measurements of 1–4AP in chloroform exhibit
a short lifetime (f = 1–2 ns) when monitored at respective emission maximum upon
excitation at 375 nm (Figure 3.11). While 2–4AP in chloroform shows a longer lifetime
(ca. 3–5 ns) when monitored at a longer wavelength (500–550 nm) indicating the
Figure 3.12. Shows the fluorescence excitation spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D)
2”AP; (E) 3AP and (F) 4AP in CHCl3 as compared to absorption spectrum.
Table 3.7. Shows the photophysical properties of 1-4AP derivatives.
a a a (ns) b b b (ns)
abs f a f ak ak abs f f b bk bk
f r nr f r nr
(nm) (nm) [Amplitude](%) (nm) (nm) [Amplitude](%)
150.1
P 337 393 0.75[143] [100][ 5 x 106 1.6 x 106 386 472 22.97 [100] 0.67[89] 2.9 x 107 1.4 x 107
144]
574.6 [15.7],
1.39 [93]
1AP 359 412 0.004 2.9 x 106 7.3 x 108 414 518 54.43 [68.5], 0.006 2.6 x 103 4.3 x 102
0.98 [7]
2873 [15.8]
1.39 [93]
426 5.8 x 106 7.3 x 108
0.65 [7] 9.68 [46.5],
2AP 373 0.008c 0.7[3] 426 602 23.19 [30.9], 0.325 1.9 x 107 4.0 x 107
510 1.35 [96] - - 2.94 [22.6]
3.0 [1]
1.3 [80]
420 1.5 x 106 7.3 x 108
1.62 [20] 3.95 [38.6],
2’AP 369 0.002c 0.8 [1] 430 567 19.55 [39.2], 0.030 1.8 x 106 5.0 x 107
530 1.36 [98] - - 1.07 [22.2]
4.22 [1]
1.4 [97]
413 5.8 x 106 7.2 x 108
0.6 [3]
3.47 [34.9],
2”AP 375 0.008c 0.8 [1] 441 631 0.063 6.0 x 106 8.0 x 107
11.57 [65.1]
535 1.4 [98] - -
4.9 [1]
431 1.2 2.5 x 106 8.3 x 108
22.48 [8.4],
3AP 388 0.003c 4.1 [67] 471 645 0.277 2.7 x 107 7.0 x 107
550 - - 4.57 [91.6]
1.5 [33]
435 0.98 2.0 x 106 1.0 x 109 1.17 [10.3],

4AP 407 0.002c 486 646 2.78 [46.9], 0.071 1.4 x 107 1.8 x 108
0.85 [55]
535 - - 6.11 [63.4]
3.8 [45]
achloroformsolution; bcrystalline state; abs – absorption; f – fluorescence; coverall quantum yield. Observed increase in the rate of radiative decay for crystalline 2, 2’ and
2’’AP when compared to 2, 2’ and 2’’AP in solution is indicative of the formation of ‘J’ type aggregate.
a) 1.0
b) 1.0
(a. u.) Fluorescence intensity (a. u.
Fluorescence intensity (a. u.

Fluorescence intensity (
Fluorescence intensity (
0.8 3.3 M 0.8
3
0.8 3.3 M 0.8 16.6 M
1
16.6 M
0.6 MM
49.93.3 0.6
4
49.9 M M M
83.316.6
0.6 0.6
49.9 M 8
Chapter 3-Engineering the solid-state packing of carbonylpyrene 83.3 M H-C,
via C-H 0.4
C-H O and - interactions
83.3 M
0.4
for 101
0.4 0.4
tuning opto-physical properties 0.2 0.2
0.2 0.2
0.0 0.0
400 450 500 550 600 650 400 450 500 550
A)
a) 1.0 B)
b) 1.0
0.0
C) 1.0
0.0 Wavelength (nm) 1.0 Wavelength (nm
d)
Fluorescence intensity (a. u.)

(a. u.) (a. u.)
1.0
400 450 500
Wavelength (nm)
550 600 c)
650
1.0
400 450 500
Wavelength (nm)
550 600 650
d)
(a. u.)

b) intensity
0.8 3.3 M c) 0.8 0.8 3.3 M 0.8 3.3
intensity
1.0
3.3 M 16.6 M
16.6 M 0.8 3.3 16.6
M M 0.8 3.3 M 16
intensity
0.6 49.9 M 0.6 M M 0.6 49.9 M 0.6 49
3.3 M 0.8 16.6 49.9 16.6 M
intensity
3.3MM
83.3 83.3 M 83
16.6 M M M
49.9 83.3 49.9 M
Fluorescence
Fluorescence
0.6 0.6
16.6 M
49.9 M 0.4
0.6 0.4 83.3 M 0.4
83.3 M 0.4
Fluorescence intensity (a. u.) Fluorescence

49.9 M
83.3 M
(a. u.) (a. u.)Fluorescence
0.4 0.4
0.2
83.3 M 0.2 0.2 0.2
0.4
0.2 0.2
0.0
0.2 0.0 0.0 0.0
400 450 500 550 600 650 400 450 500 550 600 650 400 450 500 550 600 650 400 450 500 550
1.0 Wavelength (nm) 1.0
0.0 Wavelength (nm) 0.0 Wavelength (nm) Wavelength (n
c)
D) 0.0 d) 400 450 500 550 600 650
e) 1.0
400 450 500
Wavelength (nm)
550 600 650 700
f) 1.0

Wavelength (nm)
E)

450 500 550 600 650 400 450 500
M
3.3(nm)
550 600 650
3.3 M F) 3.3
Wavelength (nm) 0.8 Wavelength e) 0.8
f) 1.0
3.3 M
intensity
1.0
d) 1.0

16.6 M 16.

16.6 M 0.8 3.3 MM
16.6
0.8
49.9 M M
3.3M 49.
3.3 M 0.6
0.8 3.3 M 0.6
0.8
49.9 0.8 49.9M
16.6 M
MM
intensity
83.3 M 16.6 83.

83.3M
83.3 0.6
16.6 M 16.6 M 0.6 49.9 M
Fluorescence
49.9 M
49.9 M 0.4
0.6 49.9 M 0.4 0.6 83.3 M
0.6
83.3 M
83.3 M 83.3 M 0.4 0.4
Fluorescence
0.2
0.4 0.2 0.4
0.4
0.2 0.2
0.0
0.2 0.0 0.2
400 450 500 550 600 650 0.2 400 450 500 550 600 650 700
0.0 0.0
Wavelength (nm) Wavelength (nm) 400 450 500 550
400 450 500 550 600 650 700
e) 0.0
1.0
f) 1.0
0.0 0.0 Wavelength (nm) Wavelength (nm
(a. u.) (a. u.)
450 500 550 600 650 400 450 500 550 600 650 700 400 450 500 550 600 650
Wavelength (nm)
400 450 500
3.3 M 550 600 650 700
Wavelength (nm)
Wavelength (nm) 3.3 M Wavelength (nm)
0.8 16.6 M
f) 0.8
1.0
16.6 M
intensityintensity
M M
3.349.9 49.9 M
3.3 M 83.3 M
16.6 MM 0.6
16.6 MFigure 3.13. Concentration dependent emission spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D)
0.6
0.8
83.3
49.9 M
Fluorescence
49.9 M
0.4
0.6 83.3 M 0.4
83.3 M
Fluorescence
0.2
2”AP; (E) 3AP and (F) 4AP in CHCl3 solution on exciting at 350 nm. 0.2
0.4
0.0
0.2 0.0
400 450 500 550 600 650 700 400 450 500 550 600 650
0.0
450 500
Wavelength (nm)
550 600
possibility of aggregation.
650 700
Wavelength (nm) Emission wavelength dependent excitation (Figure 3.12) in 400 450 500 550 600 650
combination with concentration dependent emission (Figure 3.13) and excitation
(Figure 3.14) spectra confirms the existence of ground state aggregate in 2-4AP in
A) B) C)
D) E) F)
Figure 3.14. Concentration dependent excitation spectra of (A) 1AP; (B) 2AP; (C) 2’AP; (D) 2”AP;
(E) 3AP and (F) 4AP in CHCl3 solution while monitoring at 500 nm (for 1AP and 2”AP) and 550 nm
(for 2AP, 2’AP, 3AP and 4AP).

CHCl3.
In the crystalline state, 1–4AP exhibited diverse colours ranging (Figure 3.2, Row
III) from pale yellow–yellow–orange resulting in a red-shift of 100 nm in the
absorption maximum of 4AP when compared to P (Figure 3.15A). Upon excitation at
350 nm, 1–4AP exhibited a remarkable red-shift, for example 174 nm in the case of
4AP, in the emission maximum when compared to P (Figure 3.2, Row IV and Figure
3.15B&D). Red-shift in the excimer-like fluorescence of 1–4AP could be attributed
174 nm
A) B)
100 nm
C) D)
Figure 3.15. Shows the normalised (A) absorption; (B) fluorescence emission spectra of crystalline 1-
4AP derivatives; excitation wavelength is 350 nm and (C) fluorescence decay profile of crystalline 2-
4AP derivatives and the corresponding inset shows fluorescence decay profile of crystalline 1AP,
excitation wavelength is 375 nm and emission monitored at 518 nm (1AP); 602 nm (2AP); 567 nm
(2’AP); 631 nm (2”AP); 645 nm (3AP) and 646 nm (4AP) and (D) CIE colour diagram of fluorescence
emission for crystalline 1-4AP derivatives.

to a combination of additional conjugation from acetyl groups and an increase in the
extent of overlap between the adjacent pyrene moieties[107]. A significant red-shift in
the excitation spectra of 1–4AP when compared to the corresponding absorption
spectra is indicative of ground state interaction between the vicinal pyrene units
(Figure 3.16). A slip-stacked arrangement between the adjacent pyrene units in the
crystalline 2, 2’ and 2’’AP in combination with enhanced f, f and kr when compared
to that in solution indicate the possibility of J-like aggregates and/or excimers of
pyrene (Figure 3.15C and Table 3.7)[145-147]. Aggregate induced enhanced emission
(AIEE) due to restricted motion of the flanking acetyl groups could also result in the
enhanced fluorescence of the crystalline 2, 2’ and 2’’AP[148, 149]. Enhanced f in 3–
4AP could be attributed to a combination of AIE, ground state aggregation and cross-
A) B) C)
D) E) F)
Figure 3.16. Shows fluorescence excitation spectra of crystalline (A) 1AP; (B) 2AP; (C) 2’AP;
(D) 2”AP; (E) 3AP and (F) 4AP as compared to absorption spectra. Absorption spectra of
crystalline 1-4AP derivative are reproduced for comparison with excitation spectra. Emission
maxima, where the excitation spectra are monitored, are indicated in the bracket.
dipole arrangement of the adjacent pyrene moieties as reported earlier[67, 142, 150].
Among all the crystalline derivatives 1–4AP, nonlinear increase in the emission
maximum of 3–4AP could be a consequence of orbital overlap between the adjacent
pyrene units from near-orthogonal arrangement.
Thus in this effort, progressive acylation of pyrene resulted in a remarkable
decrease in the interplanar angle between two neighbouring units causing significant
red-shift in the solid-state fluorescence. This allowed us to employ the combination of
steric and conjugation effects of benzoyl units of pyrene based systems. The significant
dimension of the benzoyl unit could potentially perturb strong π–π interactions
between the nearest pyrene units.
3.2.5. Synthesis and crystallization
Adding stoichiometric quantity of benzoyl chloride to a solution of pyrene (P)
and AlCl3 in carbon disulfide (CS2) at ambient temperature rendered the benzoyl
derivatives (1–4BP) in low-moderate yields (Figure 3.17, Row1). Though Harvey and
co-workers[151] reported 1BP, 2BP and 2’BP, the synthesis of 2’’BP, 3BP and 4BP are
yet to be explored. Single crystal X-ray analyses (SCXRD) of 1–4BP were not reported
earlier. SCXRD analyses were performed on 0.20 x 0.20 x 0.15 mm crystalline samples
obtained through slow evaporation of 1–4BP from a varying composition of
chloroform:acetone mixtures. Benzoyl derivatives 1BP (P-1), 2BP (P-1) and 3BP (P-1)
yield solvent free triclinic crystal system while 2’BP (P21/n), 2”BP (C2/c) and 4BP
(P21/n) exhibit solvent free monoclinic crystal system (Figure 3.17, Row III, Table 3.8).
I)
+ + + + +
P 1BP 2BP 2’BP 2”BP 3BP 4BP

II)
a) b) c)
d) e) f)
III)
Figure 3.17. Row I: Molecular structure of 1–4BP; Row II: close packing arrangement in the
crystal (a) 1BP; (b) 2BP; (c) 2’BP; (d) 2’’BP; (e) 3BP and (f) 4BP; Row III: photographic image
of the crystals in daylight (above) and under UV illumination (below).
2.3.6. Frontier molecular analysis and steady state studies
Frontier molecular orbital (FMO) analysis, cyclic voltammetric, UV-Vis
absorption and emission measurements were employed to investigate the extent of
perturbations in pyrene imparted by incremental benzoyl groups. FMO analyses of 1-
4BP shows that the electron density of HOMO (Figure 3.18A) is distributed in pyrene
units while electron density of LUMO is mostly localized on pyrene chromophore

Table 3.8. Shows crystallographic data and refinement parameters for crystalline 1-4BP derivatives.
1BP 2BP 2’BP 2”BP 3BP 4BP
Formula C23 H14 O C30 H18 O2 C30 H18 O2 C30 H18 O2 C37 H22 O3 C44 H26 O4
formula wt 306.34 410.44 410.44 410.44 514.55 618.65
colour, shape Yellow Yellow Yellow Yellow Yellow Orange
dimens, mm 0.20x0.2x0.15 0.20x0.15x0.10 0.25x0.20x0.15 0.20x0.15 x0.10 0.20x0.15x0.10 0.20x0.10x0.10
crystal system Triclinic Triclinic Monoclinic Monoclinic Triclinic Monoclinic
space group, Z P-1, 2 P-1, 2 P21/n, 2 C2/c, 8 P-1, 2 P21/n, 2
a, Å 8.0024 10.0326 5.4689 25.1722 8.9515 5.6503
b, Å 9.6519 10.6238 8.2510 8.4269 11.9373 20.897
c, Å 10.0837 11.6287 22.5720 19.6579 14.2375 12.787
α, deg 102.8140 94.4890 90.00 90.00 104.703 90.00
β, deg 96.5760 99.490 95.604 99.8860 102.280 101.506
γ, deg 91.4730 117.2630 90.00 90.00 109.581 90.00
V, Å3 753.40 1069.82 1013.67 4107.99 1310.36 1479.5
temp, K 296 296 296 296 296 293
dcalcd, g/cm-3 1.349 1.274 1.344 1.326 1.303 1.388
no. of reflections collected 11056 15706 7234 15377 16670 14254
no. of unique reflections 2644 3761 1732 3604 3736 3578
max , deg 50 50 50 50 50 50
no. of parameters 217 289 145 290 361 217
R1, wR2 (I I)) 0.0377, 0.1208 0.0408, 0.1147 0.0337, 0.0955 0.0482, 0.1237 0.0421, 0.1140 0.0403, 0.1084
R1, wR (all data) 0.0511, 0.1458 0.0503, 0.1292 0.0427, 0.0955 0.0711, 0.1600 0.0855, 0.1610 0.0623, 0.1253
goodness of fit 1.151 1.067 1.039 1.155 1.082 1.003
CCDC number 1440151 1440152 1440153 1440154 1440155 1440156

A) B) 4BP
3BP
2BP
Energy (eV)
2''BP
2'BP
1BP
1BP 2BP 2’BP 2’’BP 3BP 4BP -2 0 2

C) D) Voltage (V)
0.6 0.09
1BP
2BP
Absorbance (a. u.)
2'BP
2''BP 0.06 0
0.4 3BP
 O. D.
4BP
P
0.03 5 s
0.2
0.00
0.0
250 300 350 400 450 400 500 600 700
Figure 3.18. (A) Frontier molecular orbital (FMO) analysis of 1–4BP calculated from the
B3LYP/6-311G**+ level of theory. Lower and upper plots represent the HOMOs and LUMOs,
respectively; (B) cyclic voltammograms of 1–4BP in acetonitrile; (C) absorption spectra of 1–
4BP; the area filled spectrum (grey) represents the absorption spectrum of pyrene[152] and (D)
nanosecond transient absorption spectrum of 4BP in chloroform.
with a moderate extension to the carbonyl group(s). Low-lying excited electronic
states mainly results from well-described * transitions with a minor contribution
from n–* character. A decrease in the HOMO-LUMO gap from 3.59 eV (1BP) to
3.18eV (4BP) is attributed to the increase in the effective conjugation due to carbonyl
groups on the pyrene unit (Table 3.9). Cyclic voltammetry (0.1 M nBu4NPF6 in
acetonitrile) of 1BP (Figure 3.18B) exhibits oxidation peak at 1.47 V while reduction
peak appear at -1.50 V. Decrease in the HOMO-LUMO gap of benzoylpyrenes (2.97eV

Table 3.9. Experimental (electrochemical) and calculated energy levels of 1-4BP.
Energy levels (eV) Energy levels (eV)

ox red
Eon Eon EHOMO ELUMO Egap EHOMO ELUMO Egap
(V)a (V)a (eV)a (eV)a (eV)a (eV)b (eV)b (eV)b
1BP 1.47 -1.50 -6.27 -3.30 2.97 -5.79 -2.20 3.59
2BP 1.57 -1.20 -6.37 -3.60 2.77 -5.89 -2.42 3.47
2’BP 1.61 -1.35 -6.41 -3.50 2.91 -6.03 -2.61 3.42
2’’BP 1.58 -1.33 -6.38 -3.50 2.88 -5.86 -2.30 3.56
3BP 1.67 -1.13 -6.47 -3.67 2.80 -6.06 -2.69 3.37
4BP 1.61 -1.0 -6.41 -3.80 2.61 -6.28 -3.10 3.18

a experimental data; bcomputational data
for 1BP; 2.61eV for 4BP; Table 3.9) in comparison to P (3.37 eV) is in agreement with
the FMO analysis[153].
Steady state absorption spectra of 1-4BP in chloroform exhibit two distinct
bands: a band centered around 250-300 nm and another around 300-425 nm (Figure
3.18C). Time-dependent density functional theory (TDDFT)[87, 88] calculations
suggest that observed bands are a combination of several electronic transitions (Table
3.10) with the longer wavelength band due to * transition. max of long-wavelength
transition of 1BP in chloroform is red-shifted by 12 nm compared to P. 2-4BP display
remarkable red-shift in the long-wavelength, which could be attributed to the increase
in number of benzoyl group(s). Upon excitation at 380 nm, 1BP in chloroform exhibits
emission band centered around 450 nm (Figure 3.19A, Table 3.11). The emission
maximum is ca. 50 nm red-shifted in comparison to P under similar conditions.
However, further increase in the number of benzoyl groups, the emission maximum
Table 3.10. Excitation energy, oscillator strength, main transition orbitals and their
contribution calculated for 1-4BP using TDDFT (B3LYP/6-311G**++).
Excitation Oscillator Main

State (nm) Contribution
Energy (eV) strength (f) transition orbital
T4 3.35 369.83 HOMO→LUMO+1 0.48
T3 3.25 381.65 HOMO-1→LUMO 0.58
T2 2.96 418.89 HOMO-2→LUMO 0.58
T1 2.02 614.73 HOMO→LUMO 0.65

1BP
S4 3.93 315.81 0.0764 HOMO→LUMO+1 0.64
S3 3.63 341.64 0.0162 HOMO→LUMO+2 0.40
S2 3.47 356.84 0.0079 HOMO-2→LUMO 0.60
S1 3.20 387.36 0.3176 HOMO→LUMO 0.67
T4 3.13 396.21 HOMO-1→LUMO 0.59
T3 2.96 418.67 HOMO-3→LUMO 0.41
T2 2.94 422.04 HOMO-2→LUMO 0.54
T1 1.93 642.01 HOMO→LUMO 0.67

2BP S4 3.59 359.84 0.0 HOMO→LUMO+1 0.47
S3 3.52 352.53 0.0138 HOMO-1→LUMO 0.55
HOMO
S2 3.23 383.43 0.0426 0.68
→LUMO+1
S1 3.15 393.45 0.2865 HOMO→LUMO 0.66
T4 3.15 393.51 HOMO-1→LUMO 0.67
T3 2.96 418.40 HOMO-3→LUMO 0.51
T2 2.91 425.98 HOMO-2→LUMO 0.49
T1 1.93 643.61 HOMO→LUMO 0.67

2’BP
S4 3.52 352.17 0.0 HOMO→LUMO+1 0.69
S3 3.45 359.48 0.0 HOMO-2→LUMO 0.56
S2 3.43 361.18 0.0314 HOMO-3→LUMO 0.55
S1 3.08 402.01 0.5307 HOMO→LUMO 0.68
HOMO-
T4 3.15 393.51 0.67
1→LUMO
2’’BP
T3 2.96 418.40 HOMO-3→LUMO 0.51
T2 2.91 425.98 HOMO-2→LUMO 0.49

T1 1.93 643.61 HOMO→LUMO 0.67
S4 3.48 355.85 0.0065 HOMO→LUMO+1 0.50
S3 3.44 360.60 0.0074 HOMO-3→LUMO 0.58
S2 3.41 363.81 0.0009 HOMO-2→LUMO 0.47
S1 3.08 402.55 0.4693 HOMO→LUMO 0.68
T4 2.99 413.82 HOMO-4→LUMO 0.42
T3 2.93 423.53 HOMO-3→LUMO 0.40
T2 2.89 428.94 HOMO-2→LUMO 0.42952
T1 1.87 662.37 HOMO→LUMO 0.68

3BP
S4 3.45 359.22 0.0018 HOMO→LUMO 0.42
S3 3.39 365.66 0.0079 HOMO-3→LUMO 0.36
S2 3.33 372.29 0.0006 HOMO-2→LUMO 0.54
S1 3.0 413.15 0.5936 HOMO→LUMO 0.69
T4 2.96 418.66 0.31

HOMO→LUMO
HOMO--
T3 2.91 425.48 0.44
3→LUMO
T2 2.91 426.32 HOMO-1→LUMO 0.41

4BP
T1 1.86 667.46 HOMO→LUMO 0.68
S4 3.39 366.28 0.0 HOMO-3→LUMO 0.52
S3 3.37 367.48 0.0059 HOMO-1→LUMO 0.51
S2 3.35 369.67 0.0073 HOMO-2→LUMO 0.55
S1 2.96 418.61 0.5504 HOMO→LUMO 0.68
remains unchanged (ca. 450 nm). Very low fluorescence quantum yield was observed
for 1-4BP f1.0%, Table 3.11) in chloroform when compared to P (f = 65%)[92].
Picosecond time-resolved fluorescence measurements of 1–4BP indicate very
short lifetime (<100 ps pulse width at ex = 375 nm) when monitored at respective
emission maxima (Figure 3.19B). In order to rule out the possibility of aggregates of 1-
4BP in chloroform (0.1-1 M), we monitored the lifetime at the far red shifted emission.
Table 3.11. Shows the photophysical properties of 1-4BP derivatives.
a
k† a
k Fl(ns)
b b
k b
k
a
Abs Fl
a
Ph
a
r nr
a
Ph T
a Abs
b b
Fl r nr
a
Fl 8 9
a
T (Amplitude) b
f 8 9
(nm) (nm) (nm) (10 s-1) (10 s ) -1 (s) (s) (nm) (nm) (10 s-1) (10 s-1)
(%)
P 337[91] 393[91] 600[154] 0.65*[81] 75 92.5 - 0.38*[81] 5.0¶[4] 386[89] 472[89] 22.97 (100) 0.68[89] 0.29 0.01
1=0.73 (6.08)
1BP 349 444 510 0.01 1.56 9.84 23.2 0.48 2.1 500 620 2=2.49 (81.98) 0.261 0.59 0.17
3=8.54 (11.95)
1=0.61 (8.67)
2BP 395 434 527 0.011 1.0 9.90 26.7 0.41 1.4 426 552 2=2.71 (64.67) 0.149 0.31 0.18
3=6.98 (26.66)
1=3.33 (59.36)
2’BP 394 424 562 0.005 0.49 9.95 27.1 0.36 1.9 430 607 0.177 0.39 0.18
2=5.66 (40.64)
1=3.02 (68.75)
2”BP 392 426 565 0.007 0.67 9.93 29.9 0.39 2.0 420 577 0.162 0.35 0.18
2=6.33 (31.25)
1=0.3 (22.07)
3BP 397 428 633 0.005 0.49 9.95 25.2 0.35 3.3 426 524 2=2.40 (57.25) 0.032 0.16 0.22
3=6.37 (20.68)
1=0.24 (3.36)
4BP 404 429 634 0.006 0.58 9.99 21.5 0.33 2.4 446 490 2=2.05 (0.22) 0.021 0.58 2.69
3=0.02 (96.42)
*within experimental error; ¶millisecond (ms); achloroform solution; bcrystalline state; Abs – absorption; Fl – fluorescence; Ph  phosphorescence; †Fl for 1-4BP in chloroform is approximated to
100 ps (pulse duration of the excitation source) for qualitative analysis of rate of radiative and non-radiative decay. Actual rate of radiative decay (kr) for 1-4BP in chloroform can only be faster than
the estimated value, however, used exclusively for qualitative purpose. Observed decrease in the rate of radiative decay for crystalline 1-4BP when compared to 1-4BP in solution is indicative of
the formation of ‘H’ type aggregate.
Figure 3.19. Shows the (A) fluorescence spectra; ex =380 nm, area filled graph (grey colour)
represent the emission spectrum of pyrene in CHCl3; (B) fluorescence decay; ex = 375 nm and
(C) phosphorescence spectra; ex = 380 nm of 1-4BP derivatives in ethanol.
Time-resolved measurement at the longer emission wavelength exhibited a very short
lifetime (<100 ps pulse width at ex=375 nm) similar to that observed at the respective
emission maxima. An obvious shoulder peak at around 550 nm was observed in the
emission spectrum of 2’’BP. Wavelength dependent time-resolved fluorescence and
excitation spectra invalidates any possibility of aggregates of 2’’BP in solution state
under these conditions.
As stated above, low f for 1-4BP could result from an efficient intersystem
crossing (ISC) induced by strong mixing of nearly-degenerate singlet and triplet states
(Figure 3.18D and Table 3.11). ISC efficiency of 1-4BP was investigated by employing
nanosecond time-resolved absorption spectroscopy (Table 3.11). Upon excitation at
355 nm, 1BP exhibits absorption maximum at 520 nm corresponding to triplet-triplet
transition of pyrene[90] having a lifetime of 2.1 s. Similar features for triplet-triplet
absorption were also observed for 2-4BP (Table 3.11). Estimation of triplet quantum
yield (T) of 1BP based on triplet–triplet energy-transfer to - carotene shows a value
of 48% (Figure 3.18D and Table 3.11). We observed that T decreases with increase in
number of benzoyl groups (Table 3.11). Time-gated emission measurements of 1-4BP
in ethanol at 77K show extremely weak phosphorescence when excited at 380 nm
(Figure 3.19C and Table 3.11). With increase in number of benzoyl groups, systematic
red-shift from 510 to 634 nm in the phosphorescence emission maximum was
observed. In addition, non-radiative pathways could also operate to cause
significantly reduced fluorescence quantum yield in 4BP in chloroform when
compared to P. Bond rotations from benzoyl functional groups can contribute to
energy dissipative pathways.
2.3.7. Crystal packing of 1-4BP
Having established the photophysical properties of 1-4BP in solution, further
efforts were made to correlate the optical properties in the crystalline state. Detailed
analyses of single crystal X-ray structure decipher the role of terminal benzoyl groups
in impeding the pyrene-pyrene nearest-neighbour interactions in crystalline 1-4BP.
Single crystal X-ray analysis of 1BP shows an interplanar distance () of 3.50 Å
between the two nearest pyrene units having a transverse slip (along the molecular
short axis of the pyrene unit) of 0.69 Å and a longitudinal slip (along the molecular
long axis of the pyrene unit) of 0.93 Å. Observed transverse/longitudinal displacement
complements the phenyl rings to adopt an end to face (CH~2.9Å interaction with
-electron cloud of the neighbouring pyrene unit. With increase in the number of
benzoyl groups in 2-4BP, a progressive rise in the steric contribution causes an
increase in the transverse/longitudinal displacement of the vicinal pyrene units in the

4BP
3BP
2’’BP
2’BP
2BP
1BP
Figure 3.20. Shows the gradual increase in the traverse/longitudinal shift between nearest
pyrene molecules in the crystalline 1-4BP derivatives.
crystal structure (Figure 3.20&3.21; Table 3.12). In 4BP, the bulky benzoyl hampers the
strong aggregation, inducing a transverse shift (5.65 Å), prohibiting any -contacts
A) B) C)
D) E) F)
Figure 3.21. Shows the aerial overlap between adjacent pyrene units in close packing of (A)
1BP; (B) 2BP; (C) 2’BP; (D) 2”BP; (E) 3BP and (F) 4BP.
Table 3.12. Geometries in the face-to-face -stacked arrangements in crystalline 1-4BP.
 overlap
d [Å][D] d [Å][T] d [Å][L]
stacking [][O]
P 3.53 2.09 0.0 39.91
1BP 3.49 0.69 0.93 45.92
2BP 3.59 0.0 3.72 11.65
2’BP 3.49 1.23 3.80 7.66
3.35 7.79 0.68 0.0†

2’’BP
3.35 0.23 3.43 22.33*
3BP 3.36 5.41 0.0 1.84
4BP 3.47 5.65 0.0 0.95

[D] Separation between the mean planes of pyrene; [T] Transverse; [L] Longitudinal displacement between
adjacent pyrene units; [O] Ratio of the area of overlapped units of pyrene aromatic ring in the crystal
structure is calculated as the overlapped area divided by the whole area of the pyrene rings. †Lack of
orbital overlap between two vicinal pyrene units indicates that the observed red-shift in emission
maximum of crystalline 2’’BP could arise from other possible electronic interactions, such as pyrene-
benzoyl orbital interactions; *% overlap of pyrene and phenyl is calculated; the phenyl group is
interdigitated between vicinal pyrene units at a stacking distance () of 3.8Å
between neighbouring pyrene units. The longitudinal and transverse offset imparts
different degree of orbital overlap between the pyrene units that are separated at their
van der Waals distances (ca. 3.35-3.59 Å) in crystalline 1-4BP (Figure 3.17, row II, Table
3.12). This intermolecular offset of vicinal pyrene units reduces the interaction
that attributes to the observed decrease in the orbital overlap from 45.92% (1BP) to
0.95% (4BP). Interplanar C–HO[155] contacts support the pyrene units for an
extended interaction along all axis in the crystalline arrangement of 1-4BP (Figure
3.22).
A) B)
C)
D)
E) F)
Figure 3.22. Shows the C–HO interactions in the crystal packing of (A) 1BP; (B) 2BP; (C)
2’BP; (D) 2’’BP; (E) 3BP and (F) 4BP.
2.3.8. Photophysical properties of crystalline 1-4BP
Intrigued by the sterically controlled longitudinal/transverse shift of
intermolecular group vicinal pyrene units, further efforts were made to explore the
photophysical properties of crystalline 1-4BP. Diverse colour in the crystalline 1-4BP
ranging from pale yellow-yellow-orange red (Figure 3.17, Row III) were observed due
to intermolecular offset of vicinal pyrene units in the crystalline state. Diffuse
reflectance absorption spectrum of crystalline 1-4BP exhibits a broad band centered
around 350-450 nm, with an additional absorption tail extending to 500 nm in 1BP
A) B) 148 nm
1.0 1BP
P 2BP
4 1BP 2'BP
Absorbance (a. u.)

2BP 2"BP
Intensity (a. u.)

3BP
2'BP
4BP
2''BP P
3BP
4BP 0.5
2
0 0.0
300 400 500 600 400 500 600 700
C)
D)
Figure 3.23. (A) Absorption; (B) fluorescence spectra of crystalline 1–4BP derivatives; λexc =
380 nm; the area filled spectrum (grey) represents the absorption and emission spectra of
crystalline pyrene[156]; (C) fluorescence decay profile of crystalline 1-4BP; exc =375 nm and
emission wavelength monitored and (D) CIE colour diagram of fluorescence emission for
crystalline 1-4BP derivatives.
(Figure 3.23 and Table 3.11). Presence of benzoyl group(s) results a red-shift in the UV-
Vis absorption, for example 114 nm (1BP) and 60 nm (4BP), when compared to
crystalline P. Upon excitation at 380 nm, crystalline 1BP exhibits a broad emission
band with the maximum centered at 620 nm red-shifted by 148 nm compared to
crystalline P. A systematic blue-shift in the emission maximum was observed upon
further increase in number of benzoyl groups, when compared to crystalline 1BP
(Figure 3.17, Row III; Figure 3.23B&D, Table 3.11). In spite of the significant -overlap
(; 39.91%) in absorption and emission spectra of crystalline P, a blue-shift in the
emission wavelength was observed when compared to crystalline 1-4BP. A marked
increase in the separation (d3.53 Å) between the molecular planes of vicinal
pyrene units in crystalline P (Table 3.12) when compared to the crystalline BP
derivatives could cause the blue-shift in the emission spectrum. Observed differences
in the emission maxima for crystalline 1-4BP could be a combined consequence of
different i) degree ofoverlap and ii) distance between the molecular planes of the
adjacent pyrene units. However, contributions from non-nearest neighbour can also
contribute to overall electronic coupling that can influence the peak positions in
emission spectra. Significant red-shift in the emission wavelength dependent
excitation spectra compared to the corresponding steady-state absorption spectra of
crystalline 1-4BP suggests the possible ground state interaction between the vicinal
pyrene units (Figure 3.24)[117]. Substantially red-shifted dimer/excimer like emission
of 1BP could arise from significant orbital overlap (; 45.92%) between the nearest
pyrene units. Nearly slipped out (; 0.95%) pyrene-pyrene stack along the
molecular long axis in 4BP results in a monomer-like emission possessing vibronic
features.
Upon excitation at 375 nm, picosecond time-resolved fluorescence
measurements of crystalline 1BP shows tri-exponential decay having the lifetime of
2.5 ns (82%), 8.5 ns (12%) and 0.7 ns (6%), when monitored at 620 nm (Figure 3.23C
and Table 3.11). Long fluorescence lifetime in crystalline 1BP when compared to that
in solution (<100 ps) could arise from excimer/ground state aggregate of neighbouring
A) Abs B) C)
Exc 440 nm
0.8 Exc 620 nm 0.08 0.08 Abs
Exc 650 nm Exc 450 nm
Intensity (a. u.)

Intensity (a. u.)
Intensity (a. u.)
Exc 750 nm Abs Exc 608 nm
Exc 550 nm
Exc 600 nm
0.4 0.04 0.04
0.0 0.00 0.00

300 400 500 600 700 300 400 500 600 300 400 500 600
D) Wavelength (nm) E) F)
0.08 0.4
Abs Abs
0.8 Abs Exc 460 nm
Exc 460 nm
Intensity (a. u.)

Exc 450 nm
Intensity (a. u.)
Intensity (a. u.)

Exc 650 nm
Exc 600 nm
0.04 0.2
0.4
0.00 0.0 0.0

300 400 500 600 300 400 500 600 300 400 500 600
Wavelength (nm) Wavelength (nm) Wavelength (nm)
Figure 3.24. Shows fluorescence excitation spectra of crystalline (A) 1BP; (B) 2BP; (C) 2’BP;
(D) 2”BP; (E) 3BP and (F) 4BP as compared to absorption spectra. Emission maxima, where
the excitation spectra are monitored, are indicated in the bracket.
pyrene units possessing different orbital overlap in the crystalline state. Similarly,
crystalline 2-4BP show tri-exponential fluorescence emission profile with a
remarkable decrease in the lifetime of the corresponding major component (Figure
3.25A; Table 3.11). A radiative decay rate constant (kr) of 1.56×108 s−1 and 0.59×108 s−1
in solution and crystalline state of 1BP, respectively, is estimated (Table 3.11). The
faster rate of radiative decay in solution vs. crystalline state was similarly observed in
2-3BP. Observed decrease in the rate of radiative decay in crystalline 1-3BP when
compared to solution state indicates the possibility of H-like aggregates and/or
excimers of pyrene. Unusual formation of fluorescent H-aggregates were observed
earlier in merocyanine dyes by Würthner and co-workers[147]. Notably, small 
contact of vicinal pyrene units in 4BP imparts a monomer-like behaviour in the
crystalline state (Figure 3.25A; Table 3.12), as reported earlier[157]. The twisted nature
A) B)
Sn Sn
Tn
ISC ISC Tn
IC IC
Energy (eV)
Fl1% Fl26%
S0 S0
Figure 3.25. (A) Indicates F (major component; □); F (●) of 1-4BP in the crystalline state;
F (‫ )٭‬of 1-4BP in solution state and % C•••C interaction (; ∆) obtained from Hirshfeld
analysis (Table 3.13) and B) Jablonski diagram depicting energy levels in solution (monomeric)
and aggregated (crystalline) state in 1BP.
of the benzoyl group(s) with respect to the plane of pyrene chromophore drastically
diminishes the aggregation of vicinal pyrene units. Observed similar rate constant in
crystalline state and solution state of 4BP confirms the monomer-like behaviour in the
crystalline state (kr ~ 0.59×108 s−1; Table 3.11&3.12). Unravelling the processes
responsible for crystallization/ aggregation induced emission is vital for the design of
new light emitting materials. Recent preliminary theoretical investigations have
offered insights on the characteristics of induced CIE in a variety of organic/inorganic
Table 3.13. Percentage of intermolecular contacts of a molecule in crystalline 1-4AP.
Interaction 1BP 2BP 2’BP 2”BP 3BP 4BP

HH % 49.9 39.3 43.9 46.3 44.4 44.3
CH % 28.3 39.2 34.7 30.3 29.9 32.6
OH % 7.8 13.8 13.7 12.5 13.8 12.0
CC % 13.5 4.9 7.5 9.9 6.6 3.3
CO % 0.0 0.5 0.2 1.4 2.2 7.2
atotal percentage of intermolecular contacts ca. 99.5% (1BP), 97.7% (2BP), 100% (2’AP), 100%
(2”AP), 96.6% (3AP), 99.4% (4AP).
chromophores[158-160]. CIE could arise as a consequence of i) electronic
(dipolar/excitonic) interactions[147, 161-164] ii) arrested vibrational/rotational
motions[165]; and/or iii) reduced solvation[166] in crystalline state. To investigate the
extent of vibrationally promoted ISC in monomer vs. dimer states, low-lying excited
electronic states of 1BP and 4BP were calculated employing TDDFT method (Figure
3.27). The energy difference between S1 and T1 states in monomeric and dimeric 1BP
found to be 1.18 and 0.94 eV, respectively. Notable lowering of T2 energy state was
also observed from monomeric (2.95 eV) vs. dimeric (2.13 eV) 1BP. Similar
observations were made in monomeric vs. dimeric 4BP. Non-significant differences in
energy gap between the close-lying singlet and triplet energy levels of dimeric vs.
monomeric 1BP and 4BP excludes the contribution of vibrational processes in CIE.
Restriction of intramolecular rotations offered to the pendent benzoyl groups in the
S4(3.9259)
S3(3.6291)
S4(3.3850)
S2(3.4745) T4(3.3525) S4(3.2664) S3(3.3739)
T3(3.2486) S2(3.3539)
S1(3.2008) S3(3.2230)
S2(3.0896) T4(3.0319) T4(2.9615) S4(2.9865)
T2(2.9598) S1(3.0657) S1(2.9618) T3(2.9140)
T3(3.0263) S3(2.8384)
T2(2.9082)
S2(2.7248) T4(2.7109)
S1(2.7244) T3(2.7048)
Energy (eV)
T2(2.1256)
T1(2.1170)
T1(2.0169) T2(1.8325)
T1(1.8575) T1(1.8324)
S0 S0 S0 S0
Figure 3.26. Energy levels diagram of monomer and dimer of 1BP and 4BP calculated from
B3LYP/6-311G**++ level of theory.

crystalline (dimeric) state of 1-4BP may facilitate enhancement in the fluorescence,
consistent with the earlier reports[148]. Hence, CIE in 1-4BP could arise due to i)
fluorescent H-like excitonic interactions; ii) arrested rotational motion of benzoyl
group(s) and/or iii) lack of solvation in the crystalline state (Figure 3.26B).
2.4. Conclusion
In summary, we modulated the extent of – overlap between vicinal pyrene units
through successive acylation/benzoylation. Unprecedented heteropolar dihydrogen
contacts (sp2 C–HH–C sp3) in organic crystals are established using QTAIM.
Hirshfeld surface analysis is indicative of an increase in  interactions and a
concomitant decrease in the  interactions with an increase in the number of acetyl
groups per pyrene unit. A combination of C–HH–C, C–HO and  interactions
facilitate the transformation of sandwich herringbone packing of P to the herringbone
arrangement in 1 and 2’AP, the brickwork arrangement in 2 and 2’’AP and columnar
stacks in 3–4AP. A systematic decrease in the interplanar angle between the vicinal
pyrene units could be attributed to the dramatic shift in the emission spectra (ca. 42–
174 nm) of crystalline 1–4AP when compared to pyrene. J-like aggregation and/or AIE
in the crystal packing of 1–4AP corroborates the moderately emissive blue–green–
orange crystals. While through the successive benzoylation, the extent of orbital
overlap between vicinal pyrene units in crystalline 1-4BP were regulated by
exploiting the steric hindrance. Progressive increment in the steric hindrance causes
an increase in the transverse/longitudinal displacement of the vicinal pyrene units. As

a result, a 48-fold reduction in the stacking between pyrene units was observed in
4BP with respect to 1BP.
Moderating the molecular stacking along with CIE through arrested
intramolecular rotations of pendent benzoyl groups may facilitates green-yellow-
orange solid-state emitters. Modulating the emission properties of organic crystalline
materials by controlling the extent of overlap through chemical strategies could
lead to the construction of high performance photo-functional materials and device.

2.5. Appendix
Pyrene (98%), acetyl chloride (98%) and aluminum chloride (99.99%) were purchased
from Sigma Aldrich and used as such without further purification. Carbon disulfide
used as a solvent for the reaction was dried and distilled by standard procedure. TLC
analysis were performed on precoated aluminum plates of silica gel 60 F254 plates
(0.25 mm, Merck) and developed TLC plates were visualized under short and long
wavelength UV lamps. Flash column chromatography was performed using silica gel
of 200-400 mesh employing a solvent polarity correlated with the TLC mobility
observed for the substance of interest. Yields refer to chromatographically and
spectroscopically homogenous substances.
Melting points (mp) were obtained using a capillary melting point apparatus
and are reported without correction. IR spectra were recorded on a Shimadzu
IRPrestige-21 FT-IR spectrometer as neat KBr pellets for all the derivatives. 1H and 13C
NMR spectra were measured on a 500 MHz and 125 MHz Bruker advanced DPX
spectrometer respectively and 1,1,1,1-tetramethylsilane (TMS) is used as the internal
standard for 1H and 13C NMR measurements. CHN analyses were carried out on an
Elementar vario MICRO cube Elemental Analyzer. All values recorded in elemental
analyses are given in percentages. High Resolution Mass Spectra (HRMS) were
recorded on Agilent 6538 Ultra High Definition (UHD) Accurate-Mass Q-TOF-LC/MS
system using either atmospheric pressure chemical ionization (APCI) or electrospray
ionization (ESI) mode.
 Spectral Measurements:
Absorption spectra were recorded on Shimadzu UV-3600 UV-VIS-NIR while
fluorescence and excitation spectra were performed on Horiba Jobin Yvon Fluorolog
spectrometers respectively. The excitation wavelength used is 350 nm unless
otherwise mentioned. Fluorescence lifetime measurements were carried out in an IBH

picosecond single photon counting system. The fluorescence decay profiles were de-
convoluted using IBH data station software version 2.1, and fitted with exponential
decay, minimizing the χ2 values of the fit to 1 ± 0.05. All spectroscopic experiments
were performed by using standard quartz cuvettes of path length 1cm for solution in
dried and distilled solvents. The excitation laser used is 375 nm with a pulse width of
less than 100 ps. 1-4AP derivatives in chloroform were found to have
lifetime significantly shorter than the excitation pulse width. The solution state
fluorescence quantum yields were determined by using optically matched solutions.
Quinine sulfate dissolved in 0.5 M H2SO4 (Φf = 0.546) is used as the standard for 1-
4AP derivatives.
Nanosecond transient absorption measurements. Nanosecond laser flash photolysis
experiments of the argon purged solutions were carried out in an Applied
Photophysics Model LKS-60 laser kinetic spectrometer using the third harmonic (355
nm, pulse duration ≈10 ns) of a Quanta Ray INDI-40-10 series pulsed Nd:YAG laser
as the excitation source. Triplet states of 1-4BP in CHCl3 were confirmed performing
the experiments with oxygen purged solutions.
Triplet quantum yields upon direct photoexcitation (355 nm) were determined by
using [Ru(bpy)]Cl2 in methanol as standard (T = 100%), with nonsaturating laser
intensities. Equal volume of 0.2 mM solution of -carotene was added to optically
matched solutions of reference and the sample. The equation for the triplet quantum
yield is given by,

𝑅𝑒𝑓 𝑅𝑒𝑓
𝑅𝑒𝑓 𝛥𝐴𝑆 𝑘𝑆𝑜𝑏𝑠 𝑘𝑜𝑏𝑠 − 𝑘0
𝛷𝑠𝑇 = 𝛷𝑇 x x x 𝑅𝑒𝑓
𝛥𝐴𝑅𝑒𝑓 𝑘𝑆𝑜𝑏𝑠 − 𝑘𝑆0 𝑘𝑜𝑏𝑠
Where, ΦTs and ΦTRef denote the triplet quantum yield of the sample and reference
respectively; ΔAS and ΔARef are transient absorption intensity of b-carotene in sample
and reference respectively; k Sobs and k S0 are decay rate of sample transient species
before and after the addition of b-carotene. k Ref Ref

obs and k 0 are decay rate of reference
transient species before and after the addition of -carotene.

Cyclic Voltammetry (CV): Electrochemical measurements were performed on a BASi
(Bioanalytical Systems, Inc.) C-3 cell stand controlled by Epsilon electrochemical
workstation. A three electrode system is then constructed constituting a glassy carbon
as the working electrode, a platinum-wire as the counter electrode, and an Ag/Ag+ (3
M NaCl) as the reference electrode. The electrochemical measurements were
conducted under nitrogen atmosphere (5 psi, 10 minutes) in a deoxygenated
anhydrous acetonitrile of tetra-n-butylammonium hexafluorophosphate (supporting
electrolyte, 0.1 M) for 1-4BP derivatives in CHCl3 with a scan rate of 50–100 mVs−1.
Calibration of the instrument was performed using the ferrocene/ferrocenium (Fc/Fc+)
redox couple as an internal standard and measured under same condition before and
after the measurement of samples. The energy level of Fc/Fc+ was assumed to be -4.8
eV with respect to vacuum. The half-wave potential of Fc/Fc+ was estimated to be 0.5
V with reference to the Ag/Ag+ electrode.
HOMO and LUMO energy levels were calculated from the following equations:
onset
EHOMO = −(Eox + 4.8) eV and (1)
onset
ELUMO = −(Ered + 4.8) eV (2)
onset onset
respectively, where Eox and Ered are the onset oxidation and reduction potentials
relative to the Ag/Ag+ reference electrode.
The electrochemical energy gap (Eg) is estimated as follows:

Eg = (ELUMO − EHOMO ) eV (3)
where ELUMO and EHOMO are the corresponding to HOMO and LUMO energy levels
calculated after converting the values in Ag/Ag+ with respect to the standard calomel
electrode (SCE) convention.
Determination of fluorescence quantum yield and radiative and non-radiative rate
constants: Solution state fluorescence quantum yields of 1-4BP derivatives were
calculated by relative quantum yield method as follows,

I OD n
⏀s = ⏀ref (I s )( ODref )(n s )2 (4)
ref s ref
wherein, ⏀s and ⏀ref are the quantum yields of sample and reference respectively,
Is and Iref are the area under the emission spectrum for sample and reference
respectively. ODs and ODref are the absorbances of sample and reference respectively
at the excitation wavelength. ns and nref are the refractive index of the solvent in
which sample and reference are taken.
Radiative (k r ) and non-radiative (k nr ) rate constants from the singlet excited states are
calculated from the fluorescence quantum yields, ⏀f.

kr
⏀f = k (5)
r +knr
The rate constants k r and k nr can be evaluated by measuring fluorescence lifetimes (f)
from TCSPC measurements. The following equations depict relation between⏀f , f,
k r and k nr .
⏀f
kr = and (6)
τf
1−⏀f
k nr = (7)
τf
a change in ⏀f could be attributed to the changes in either k r /k nr . The enhancement
in the quantum yield (⏀f ) with increased solvent polarity is due to the stabilization of
the excited states by virtue of interaction with the solvent dipoles and decrease in the
non-radiative (k nr ) rate constant.
 X-ray Crystallography
X-ray Crystallography: High-quality specimens of appropriate dimensions were
selected for the X-ray diffraction experiments. Crystallographic data collected are
presented in the supplementary information. Single crystals were mounted using oil
(Infineum V8512) on a glass fibre. All measurements were made on a CCD area
detector with graphite monochromated Mo Kα radiation. The data was collected
using Bruker APEXII detector and processed using APEX2 from Bruker. All structures
were solved by direct methods and expanded using Fourier techniques. The non-
hydrogen atoms were refined anisotropically. Hydrogen atoms were included in
idealized positions, but not refined. Their positions were constrained relative to their
parent atom using the appropriate HFIX command in SHELXL-97. The full validation
of CIFs and structure factors of 1-4AP derivatives were performed using the CheckCIF
utility and found to be free of major alert level. 3D structure visualization and the
exploration of the crystal packing of 14BP were carried out using Mercury 3.1.
 Computational Methods
Quantum Theory of Atoms in Molecules (QTAIM): The wave function for XPs were
obtained employing the geometries taken from the crystal structure using Gaussian
set of codes at B3LYP/6-311G**++ level.1 Quantum theory of atoms in molecules
(QTAIM) analysis helps to understand the description of interatomic interaction in the
single crystal X-ray structure. A bond is defined along the bond line between two
nuclei, called a bond path, along which electron density is concentrated. The bond
critical point (BCP) is a point along the bond path at the interatomic surface, where
the shared electron density reaches a minimum. The physical characteristics of the
BCPs [the electron density at BCP, (rBCP), and its Laplacian, 2(rBCP)] reveal the
approximate measure of the amount of electron density built up in the bonding region
and as such could be taken as characteristic of the bond. When 2(rBCP) < 0 and is
large in magnitude, (rBCP) is also large which means that there is a concentration of
electronic charge in the internuclear region. This is also an indication of a sharing of
electronic charge between both nuclei that defines the covalent (polar) bond. When
2(rBCP) < 0 there is a depletion of electronic charge in the internuclear region. Using
the AIM 2000 software package, the electron density was integrated over atomic
basins according to the quantum theory of atoms in molecules using PROAIM, and
thus the BCP data and the molecular graphs were obtained.
Computational methods used for calculating singlet and triplet energy levels of 1-
4BP derivatives: Ground state optimized energies and harmonic oscillator frequencies
were computed using density functional theory (DFT) employing B3LYP functional
with 6-311G**+ basis set. Vertical excitation energies were determined performing
time-dependent DFT (TDDFT) calculations at the B3LYP/6-311**+ level of theory with
Gaussian 09 program suite.
Hirshfeld analysis: Important intermolecular interactions within the crystal structure
of 1-4BP/AP were identified through Hirshfeld surface analysis using Crystal Explorer
3.1. The Hirshfeld surface is defined as a set of points in 3D space where the ratio of
promolecule and procrystal electron densities is equal to 0.5. The exploration of
intermolecular contacts is provided by mapping normalized contact distances (dnorm),
which is a function of a closest distance from the point to the nuclei interior (d i) and
exterior (de) to the surface as well as on the van der Waals radii (rvdw). 2D fingerprint
which were generated by deriving from the Hirshfeld surface by plotting the fraction
of points on the surface as the fuction of di and de which provide a visual summary of
intermolecular contacts within the crystal.
Analysis of Chromaticity Index: Coordinates (x, y, z) for chromaticity are acquired
by calculating the fractional component of the tristimulus values: x = X/(X+Y+Z), y =
Y/(X+Y+Z), z = Z/(X+Y+Z). X, Y, Z are the CIE 1931 tristimulus values. By convention,
chromicity coordinates (x, y) denote the two dimensional plot CIE 1931 colour space
chromaticity diagram.
Calculation of percentage overlap: The % overlap of closest dimer of vicinal pyrene
units in the crystalline 1-4BP is calculated using ImageJ 1.4. It can calculate area and
pixel value statistics of user-defined selections. The input geometries for the closest
dimer (.bmp file) were arranged, conforming to crystal packing thereby preserving
the relative positions and orientations of vicinal pyrene units. The ratio of the area of
overlapped moieties of pyrene aromatic rings in the crystal structures is calculated as
the overlapped area divided by the whole area of the pyrene rings.
Overlaped Area
% Overlap = [ ] × 100
Overlaped Area + Non overlaped Area
 Synthesis Details
Synthesis and characterization of 1-4AP derivatives were reported in Chapter 2.
Scheme 3.1. Shows the synthesis of benzoylpyrene (1-4BP) derivatives.

Preparation of benzoylpyrene (1-4BP) derivatives: Pyrene (10 g; 0.049 mols)
dissolved in CS2 (yellow solution, 250 mL) was maintained at ambient temperature
and subsequently anhydrous AlCl3 was added. Benzoyl chloride (27.80 g; 0.198 mols)
was then slowly syringed to the suspension. Subsequently, hydrogen chloride was
liberated. After 3 hrs the mixture was added slowly to a vigorously stirred mixture of
ice and concentrated HCl. The resulting suspension was filtered and vacuum dried
and purified through column chromatography (silica gel) to give benzoylpyrene (1-
4BP) derivatives.
1BP (yield= 5.1%) M.p. 102-105 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.40 (m, 4H),
8.43 (q, J = 9.66 Hz, 2H), 8.17 (m, 3H), 7.82 (d, J = 7.7 Hz, 2H), 7.73 (t, J = 7.2 Hz, 1H),
7.58 (d, J = 7.8 Hz, 2H). 13C NMR [125 MHz, DMSO(d6), δ]: 197.56, 138.0, 133.60, 132.82,
132.46, 130.70, 130.08, 129.07, 128.90, 128.83, 128.66, 127.25, 126.83, 126.68, 126.35,
126.04, 124.20, 124.10, 123.84, 123.55. IR (KBr, cm-1): 3037, 1651, 1595, 1506, 1446.
Elemental analysis: calcd. value for C23H14O: 90.17% C, 4.61% H; found: 90.31% C,
4.56% H. HRMS (ESI) m/z calculated for C23H14O [M]+: 306.1045, found: 306.1037.
2BP (yield= 9.4%) M.p. 164-167 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.50 (d, J = 7.7,
2H), 8.43 (d, J = 9.3 Hz, 2H), 8.32 (d, J =9.2 Hz, 2H), 8.25 (t, J = 7.7 Hz, 1H), 8.13 (s, 1H),
7.88 (d, J = 8.2, 4H), 7.71 (t, J = 7.5, 2H), 7.57 (t, J = 7.8, 4H). 13C NMR [125 MHz,
DMSO(d6), δ]: 201.94, 131.41, 131.21, 130.37, 129.87, 128.03, 127.43, 127.20, 124.39,
124.18, 123.19, 30.71. IR (KBr, cm-1): 3053, 1656, 1585, 1516, 1446. Elemental analysis:
calcd. value for C30H18O2: 87.78% C, 4.42% H; found: 87.63% C, 4.61% H. HRMS (ESI)
m/z calculated for C30H18O2 [M]+: 410.1307, found: 410.1305.
2’BP (yield= 9.6%) M.p 233-238 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.38 (d, J = 8 Hz,
2H), 8.25 (d, J = 9.5 Hz, 2H), 8.18 (d, J = 9.5 Hz, 2H), 8.10 (d, J = 7.5 Hz, 2H), 7.73 (d, J =
7.7 Hz, 4 H), 7.64 (t, J = 7.1, 2H), 7.49 (t, J =7.7 , 4H). 13C NMR [125 MHz, DMSO(d6), δ]:
202.20, 133.33, 132.31, 129.07, 128.20, 127.73, 126.39, 125.35, 123.73, 30.64. IR (KBr, cm-
1
): 3051, 1649, 1571, 1490, 1442. Elemental analysis: calcd. value for C30H18O2: 87.78% C,
4.42% H; found: 87.71% C, 4.69% H. HRMS (ESI) m/z calculated for C30H18O2 [M]+:
410.1307, found: 410.1301.
2’’BP (yield= 37.5%) M.p. 155-158 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.42 (d, J = 7.5
Hz, 2H), 8.35 (s, 2H), 8.11= (d, J = 3 Hz, 2H), 8.09 (s, 2H), 7.71 (d, J = 8.25, 4H), 7.61 (t, J
= 8.5, 2H), 7.47 (t, J = 7.25, 4H). 13C NMR [125 MHz, DMSO(d6), δ]: 197.82, 138.27, 134.29,
134.25, 132.99, 130.63, 129.43, 129.36, 128.57, 127.54, 126.14, 125.97, 126.14, 124.22. IR
(KBr, cm-1) 3051, 1654, 1595, 1446, 1446. Elemental analysis: calcd. value for C30H18O2:
87.78% C, 4.42% H; found: 87.68% C, 4.59% H. HRMS (ESI) m/z calculated for C30H18O2
[M]+: 410.1307, found: 410.1298.
3BP (yield= 18.9%) M.p. 183-187 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.63 (d, J = 9.7
Hz, 1H), 8.54 (d, J = 9.3 Hz, 1H), 8.42 (d, J = 9.2 Hz, 1H), 8.35 (s, 2H), 8.30 (d, J = 7.8 Hz,
1H), 8.23 (s, 1H), 8.89 (m, 4H), 7.85 (d, J = 7.7 Hz, 2H), 7.75 (m, 3H), 7.63 (m, 6H). 13C
NMR [125 MHz, DMSO(d6), δ]:197.18, 196.63, 196.52, 137.60, 137.48, 137.43, 135, 133.93,
133.90, 132.89, 132.65, 131.81, 130.42, 130.27, 130.26, 130.17, 129.77, 128.90, 128.88,
128.85, 128.06, 127.34, 127.22, 127.17, 126.44, 125.50, 124.50, 124.15, 123.64. IR (KBr, cm-
1): 3055, 1654, 1593, 1568, 1446. Elemental analysis: calcd. value for C37H22O3: 86.36% C,
4.31% H; found: 87.41% C, 4.45% H. HRMS (ESI) m/z calculated for C37H22O3 [M]+:
514.1569, found: 516.1552.
4BP (yield= 1.9%) M.p. 283-285 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.33 (s, 4H), 8.20
(s, 2H), 7.81 (d, J = 9.25 Hz, 8H), 7.65 (t, J = 7.85 Hz, 4H), 7.50 (t, J = 7.85 Hz, 8H). 13C
NMR [125MHz, DMSO(d6), δ]:196.93, 137.82, 134.56, 134.39, 130.80, 130.19, 129.41,
127.75, 127.46, 124.62. IR (KBr, cm-1): 3055, 1654, 1593, 1568, 1446. Elemental analysis:
calcd. value for C44H26O4: 85.42% C, 4.24% H; found: 85.63% C, 4.31% H. HRMS (ESI)
m/z calculated for C44H26O4[M]+: 618.1831 found: 618.1820.

Progressive acylation of pyrene engineers solid-state packing and colour via C–
HH–C, C–HO and – interactions
Quantum theory of atoms-in-molecules and Hirshfeld surface analyses indicated an increase in the
extent of (i) C–H⋯H–C; (ii) C–H⋯O, (iii) π–π interactions and a decrease in the extent of (i) σ–π
interaction, (ii) an interplanar angle between the vicinal pyrene units in aseries of acetylpyrene
derivatives offering blue–green–orange emissive crystals.

Crystallization induced green-yellow-orange emitters based on benzoylpyrenes
Steric hindrance due to incremental benzoyl groups causes a systematic reduction in the orbital
overlap (π–π) between vicinal pyrene units affording green-yellow-orange solid-state emitters.
Crystallization induced emission could arise from: i) electronic (dipolar/excitonic) interactions, ii)
arrested bond rotations, and/or iii) lack of solvation in crystalline 1–4BP (ΦFl ∼ 2–26%) when
compared to that in solution (ΦFl ≤ 1%).
Chapter 4
Solid-state ordering of pyrene based single crystalline
materials for high-performance organic field-effect transistors
Abstract
Pyrene-based materials possessing one-dimensional cofacial π−π stacked structural
motifs with short inter-planar distances can have favorable charge transport properties. In this
work, we have realized the switching of sandwichherringbone to lamellar/columnar
arrangement by introducing α-haloacetyl substituents in pyrene.
Though various chemical and physical strategies were employed to self-assemble the
molecules in an impressive array in the crystal structure, a direct understanding of such
molecular ordering to enhance the device performance, still remains unexplored. We evaluate
the intrinsic molecular packing on charge-transport properties of acetylpyrene (AP) based
materials. The adverse edge-to-face packing of pyrene units minimize the  overlap between
the adjacent molecules leading to high resistance to charge transfer in 1AP (847 M) and 2’AP
(332 M) when compared to the stacked face-to-face (interaction observed in the
brickwork [2AP (21 M) and 2’’AP (18 M)] and columnar [3AP (77 M) and 4AP (27
M)] arrangement. Hence the observed decrease in the resistance by an order of one magnitude
seems that the crystals with stacked packing (brickwork and columnar) are better than those
with herringbone packing. Field-effect measurement has been done on 4AP crystals, since these
are rod-like in appearance and are easy to place on the substrate-silicon wafer with 200 nm of
thermally grown oxide layer. At increasingly negative gate voltages, the mobility was found to
monotonously increasing from 0.03 to 0.18 cm2 V-1 s-1.
Salini P. S.; † Rajagopal, S. K.; † Hariharan, M* Cryst. Growth Des. [10.1021/acs.cgd.6b00919].

Chapter 4- Solid-state ordering of pyrene based single crystalline materials for high-performance organic field-effect 136
transistors
4.1. Introduction
Polyaromatic hydrocarbons (PAHs) have attracted a great deal of interest as
semiconductor materials over the past few years due to their unique processing
characteristics and improved electronic mobility[167-170]. Control of spatial
arrangement of constituent molecules in functional organic materials is of paramount
importance because face-to-face arrangement of arenes is a key attribute in the field of
organic optical and semiconductor materials[171-174]. In general, face-to-face (ππ)
stacking competes with edge-to-face (C-Hπ) interactions and the latter interactions
usually dominate the packing arrangement of PAHs. Consequently, PAHs tend to
form herringbone arrangements with negligible π-orbital overlap in the crystalline
state[107, 175-178]. Switching the herringbone arrangement (C-Hπ) of PAHs to face-
to-face lamellar/columnar arrangement by modulating molecular packing through
covalent[179, 180]/non-covalent[98] routes is a burgeoning topic of interest.
Among the PAHs, pyrene based systems are a promising class of organic
materials for optoelectronic devices[5, 181, 182]. Pyrene, because of the sandwich
herringbone arrangement, minimizes the extent of orbital overlap through ππ
interactions[183]. Albeit several approaches have been reported for constructing π-
stacked arrangements of linear polyacenes such as anthracene[184], tetracene[103,
185] and pentacene[104, 186]; constructing π-stacked columnar/lamellar
arrangements of pyrene received less attention. Major challenge is to regulate the non-
covalent interactions through rational molecular design, thereby reorganizing the

transistors
supramolecular architecture[95, 149, 187]. Among these, hydrogen bonding[188] is the
most explored, while other interactions such as the dihydrogen contacts[122] and the
halogen interactions[189, 190] have been the recent topic of interest. Our ongoing
interest to regulate the arene-arene interactions in crystalline state[113, 132, 133] and
vesicular gels[115] prompted us to explore the role of halogen interactions in
modulating the packing arrangement of pyrene. We recently tuned the extent of ππ
overlap between vicinal pyrene units through progressive acylation and achieved a
gradual transformation of sandwich herringbone to herringbone, then to lamellar and
finally to columnar arrangement[191]. However, successive benzoylation of pyrene
causes a systematic reduction in the orbital overlap (ππ) between vicinal pyrene
units owing to the steric hindrance offered by the benzoyl groups[192]. We have also
demonstrated the diverse orbital overlap between vicinal pyrene units in a group of
three regioisomeric thiazolylpyrenes where 1,3- and 1,8-substitution led to columnar
arrangement while 1,6-substitution resulted in herringbone arrangement of pyrene
units[193]. Herein, we present our efforts on haloacylation promoted switching of
sandwich herringbone to lamellar/columnar arrangement of pyrene utilizing
hydrogen bonding, halogen interactions and dihydrogen contacts.
It is generally believed that π-π stacking would be much more efficient than
herringbone stacking for the transporting of charge carriers. Lots of research has been
accomplished to prevent the C-Hπ intermolecular interactions in order to obtain
ππ stacking (lamellar structure) in the crystals through substituting at the peri-
positions of acenes. Anthony and co-workers[104] introduced triisopropylsilylethynyl

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(TIPS) groups to pentacence core which helps to stacks in a two dimensional columnar
array with significant overlap of the pentacene rings in adjacent molecules, and
demonstrated significant conductivity enhancements. Pei and co-workers[194] have
realized systematic fine-tuning of the single-crystal molecular packing of five
benzodifurandione-based oligo(p-phenylenevinylene) (BDOPV) through
incorporation of electronegative fluorine atoms on the BDOPV backbone.
Consequently, the electronic couplings for electron transfer vary from 71 meV in a
slipped stack to 201 meV in a nearly cofacial antiparallel stack, leading to an increase
in the electron mobility of the BDOPV derivatives from 2.6 to 12.6 cm2 V−1 s−1.
High transportation capabilities of charge carriers in pyrene based
semiconductors has attracted its application in p-type and ambipolar OFETs[181, 195].
The recent interests in pyrene based semiconductors is due to control over molecular
architecture that can be achieved by modifying the structure by varying the position
of substitution on the pyrene ring. Herein, we report on comparative investigation of
conductivity in systematically synthesized acyl pyrene derivatives. In our approach,
we first study the morphology of the derivatives by scanning electron microscopy
(SEM), atomic force microscopy (AFM), and tunneling electron microscopy (TEM).
Further, we determine the I-V profiles of the derivatives and use field-effect transistor
(FET) measurements to obtain the charge carrier mobility which corroborate with
theoretically predicted trend.

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4.2.1. Synthesis, characterization and crystallization of bis-haloacetyl pyrene
derivatives (XPs)
1,3- and 1,8-CP were synthesized by the Friedel-Crafts reaction[116] of pyrene
with chloroacetyl chloride and are obtained in 33 and 38 % yield, respectively (Scheme
4.1). 1,3- and 1,8-BP[196]/IP[197] were obtained in moderate yields by the
bromination/iodination of the corresponding acetylpyrene derivatives (AP)[85]
(Schemes 4.2&4.4). The nucleophilic substitution reaction of bromoacetylpyrene with
CsF resulted in corresponding 1,3- and 1,8-FP[198] in 7 and 10 % yield, respectively
(Scheme 4.3). Though the syntheses of -chloroacetylpyrenes (1,3 and 1,8-CP) and 1,8-
bromoacetylpyrene (1,8-BP) were reported by Vollmann[13] and Harvey[151]
respectively, 1,3-BP, 1,3- and 1,8-FP/IP were not explored in the literature. Single
crystal X-ray analyses of bis(haloacetyl)pyrenes (XPs) were not reported earlier. XPs
were characterized by spectroscopic and analytical techniques and their structure was
confirmed by single crystal X-ray diffraction analysis (Figure 4.1 and Table 4.1). Single
crystals of XPs except 1,8-CP, suitable for X-ray diffraction, were obtained through
slow evaporation of chloroform:hexane mixtures while that of 1,8-CP, a polymorph
of 1,8-CP, were obtained from dimethyl sulfoxide[199]. 1,3-BP/CP/IP yielded solvent
free triclinic crystal system with space group P-1 while 1,3-FP and 1,8- FP/CP/CP/BP
exhibited solvent free orthorhombic crystal system with space group Pbca, Pnma,
P212121, Pnma, Pccn, respectively (Figure 4.1 and Table 4.1).
4.2.2. Crystal structure analyses of XPs
Qualitative analyses of the single crystal X-ray structure of XPs indicate

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1,3-FP 1,3-CP 1,3-BP 1,3-IP
1,8-FP 1,8-CP 1,8-CP 1,8-BP
Figure 4.1. Single crystal X-ray structure of XPs.
intramolecular dihydrogen contacts and intramolecular C-HO hydrogen bonding
interaction in the range within their van der Waal’s radii. Dihydrogen contacts in XPs
were observed between methylenyl hydrogens and pyrenyl hydrogen within the
distance of 2.4 Å (Table 4.2.). The shortest HH interaction distance in 1,3- XP
decreases from 2.1 Å in 1,3-AP to 2.02 Å in 1,3-IP (Figure 4.2.A). Similar trend was
observed in 1,8-XP in which the shortest HH interaction distance ranges from 2.32
Å in 1,8-AP to 2.06 Å in 1,8-BP. Quantum theory of atoms in molecules analyses
(QTAIM)[139, 140] of the crystalline 1,3-BP revealed bifurcated dihydrogen contacts
with distance of 1.96 Å and 2.01 Å, respectively (Figure 4.2.B). The accumulation of
electron charge density at the (3, -1) bond critical point [BCP; b(r)0. eÅ-3and 0.09
eÅ-3, and positive value of Laplacian [2b(r)] of 1.78 eÅ-5 and 1.58 eÅ-5 with the
Chapter-4 Solid-state ordering of pyrene based single crystalline materials for high-performance organic field-effect transistors 141
Table 4.1. Crystal data and structure refinement for 1,3 and 1,8-XP.
1,3-FP 1,3-CP 1,3-BP 1,3-IP 1,8-FP 1,8-CP 1,8-CP 1,8-BP

formula C20H12F2O2 C20H12Cl2O2 C20H12Br2O2 C20H12I2O2 C20H12F2O2 C20H12Cl2O2 C20H12Cl2O2 C20H12Br2O2
formula wt 322.30 355.20 444.12 538.10 322.30 355.20 355.20 444.12
crystal system orthorhombic triclinic triclinic triclinic orthorhombic orthorhombic orthorhombic orthorhombic
space group, Z Pbca, 8 P-1, 2 P-1, 2 P-1, 2 Pnma, 4 P212121, 4 Pnma, 4 Pccn, 4
a, Å 7.4848 7.7841 7.5885 8.638 8.114 5.225 7.1129 20.8673
b, Å 15.768 8.5413 8.0425 9.748 22.950 11.280 25.621 4.5301
c, Å 24.344 12.0066 13.943 10.406 7.598 26.310 8.5925 16.8114
α, deg 90 98.129 74.493 103.296 90 90 90 90
β, deg 90 101.832 75.258 94.979 90 90 90 90
γ, deg 90 94.942 89.916 100.159 90 90 90 90
V, Å3 2873.1 768.0 791.0 831.9 1414.9 1550.7 1565.9 1589.20
temp, K 296 293 296 296 293 296 296 296
dcalcd,g/cm-3 1.489 1.536 1.864 2.146 1.513 1.520 1.506 1.854
no. of reflections
39586 11665 6110 11287 6245 6510 6241 11586
collected
no. of unique
2534 2718 2978 2927 1423 2730 1571 1407
reflections
no.of parameters 217 217 217 217 109 217 109 109
R1, wR2 0.0634, 0.0382, 0.0982, 0.0442, 0.0392, 0.0522, 0.0851, 0.0428,
(I > 2(I)) 0.1869 0.1046 0.2920 0.1474 0.1081 0.1224 0.1944 0.1203
R1, wR2 0.1107, 0.0538, 0.1295, 0.0511, 0.0502, 0.0989, 0.1815, 0.0599,
(all data) 0.2459 0.1253 0.3104 0.1626 0.1190 0.1688 0.2538 0.1366
goodness of fit 1.069 1.136 1.079 1.091 1.071 1.044 1.033 1.057
Chapter-4 Solid-state ordering of pyrene based single crystalline materials for high-performance organic field-effect 142
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A) 2.12
2.12 B)
HH distance (Å)

2.08
2.08
Intramolecular distance
2.04
2.04
Intramolecular
2.00
2.00
1.96
1.96
HCHH FCHH ClCHH BrCHH ICHH

CH3...H FCH2...H (CH2Cl)...H(CH2Br)...H(CH2I)...H
Figure 4.2. (A) Decrease in the intramolecular dihydrogen distance in 1,3-XP compared to
1,3-AP and (B) QTAIM electron density map of 1,3-BP indicating intramolecular dihydrogen
and C-HO interactions.
interaction distance of 1.96 Å and 2.01 Å, respectively, confirms the presence of
intramolecular bifurcated HH interaction in 1,3-BP. QTAIM of other XPs offered no
characteristics supporting the intramolecular dihydrogen interactions at distances less
than 2.4 Å. In addition to intramolecular dihydrogen contacts, intramolecular C-HO
hydrogen bonding interaction was observed in XPs between carbonyl oxygen and
pyrenyl hydrogen with distance ranging from 2.17 Å to 2.88 Å (Table 4.2.). Crystal
packing arrangement of XPs is shown in Figures 4.3A&B where lamellar and
columnar assembly was observed. ππ stacking, halogen interactions, dihydrogen
contacts and C(pyrene)−HO (carbonyl) hydrogen bonds act as the principal driving
forces for the molecular packing. In 1,3-XP, face-to-face lamellar/columnar
arrangement was obtained with strong ππ stacking interactions between
neighboring pyrene units with an interplanar distance of 3.52 Å (1,3-FP), 3.55 Å (1,3-
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Table 4.2. Shows the intramolecular interactions in 1,3-XP and 1,8-XP as visualized through
Mercury CSD 3.8.
Interaction d (Å)
H1H2 2.068
H1H4 2.208
13-FP H1H2 2.268
O1H7 2.205
H5 H3
O2H6 2.505
H4 H1 H2 H1H2 2.362
O2 H1H3 2.051
O1
H1H4 2.208
13-CP
H6 H1H5 2.162
H7
O1H7 2.160
O2H6 2.179
H1H3 1.964
H1H4 2.011
13-BP
O1H7 2.185
O2H6 2.189
H1H2 1.972
H1H4 2.017
13-IP
O1H7 2.182
O2H6 2.190
Interaction d (Å)
H1H2 2.091
H2
18-FP O1H7 2.639
H1 O2H8
H3
O1 H1H2 2.362
H1H3 2.088
H1H4 2.218
H7 18-CP
H1H5 2.205
O1H7 2.881
H8
O2H8 2.872
H1H3 / 2.137
O2 H1H4
18-C’P
H6 O1H7/ 2.886
H4
O2H8
H5 H1H2 / 2.061
H1H4
18-BP
O1H7/ 2.174
O2H8
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A)
1,3-FP 1,3-CP 1,3-BP 1,3-IP

Columnar π-π stack Lamellar π-π stack Columnar π-π stack Lamellar π-π stack
β- motif (= 0.73) γ- motif (= 1.25) β- motif (= 0.56) γ- motif (= 1.49)
B)
1,8-FP 1,8-CP 1,8-CP 1,8-BP

Herringbone Lamellar π-π stack Columnar π-π stack Lamellar π-π stack
(= 4.8) γ- motif (= 2.24) β - motif (= 1.07) γ- motif (= 1.21)
C)
1,3-FP 1,3-CP 1,3-BP 1,3-IP

d= 3.52 Å d= 3.55 Å d= 3.42 Å d= 3.39 Å
Figure 4.3. Close packing arrangement in (A) 1,3-XPs and (B) 1,8-XPs indicating the values
of  [(%CH)/(%CC)]. Herringbone ( 4.5), sandwichherringbone (3.2  4.0),  (1.2
2.7),  (0.46  1.0) and (C) schematic representation showing the decrease in the
interplanar distance between pyrene units in 1, 3-XPs.
CP), 3.42 Å (1,3-BP) and 3.39 Å (1,3-IP) respectively (Figure 4.3C&4.4). It is pertinent
to point out that introduction of haloacetyl group in 1,3-XP resulted in the ππ stacked
lamellar/columnar arrangement compared to the sandwich herringbone arrangement
of pyrene. Similarly as the polarizability of the halogen increases, a gradual decrease

A) B) C) D)
3.39 Å
3.55 Å 3.42 Å
3.52 Å
1,3-FP 1,3-CP 1,3-BP 1,3-IP
Figure 4.4. Shows the decrease in the interplanar distance between pyrene units in 1,3-XP.
1,3-
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in the interplanar distance was observed suggesting favorable molecular overlap. To
explore the effects of haloacetylation on the crystal packing, we have generated
electrostatic potential (ESP) maps to demonstrate the difference in charge distribution
of XPs (Figure 4.5). Within the series of haloacetylpyrenes, there is a significant
difference in charge distribution as we move from FP to IP owing to the increasing
polarizability of halogens[200]. With more polarizable halogen such as iodine, the
surface charge is more unevenly distributed on the molecular surface. Such
reorganization of surface charge distribution create an opportunity to pack in a way
to maximize the electrostatic interactions, implying that this is the weak dominant
interaction in these systems. As a result, within the series, the strength of π−π stacking
interaction increases as we move from FP to IP (Figure 4.5). A closer inspection of the
packing of 1,3-XP revealed two type of HX interactions including C(sp3)-HX and
C(sp2)-HX (Figures 4.6A,B,C&D) where C(sp3)-HX interaction in 1,3-FP (dHF:
2.50 Å andC-HF: 147), 1,3-BP (dHBr: 3.08 Å and C-HBr: 149), and 1,3-IP (dHI: 3.13
Å and C-HI: 136) leads to corresponding dimer formation in the crystalline state
while C(sp2)-HX in 1,3-FP (dHF: 2.55 Å and C-HF: 140) and 1,3-CP(dHCl: 2.94 Å
and C-HCl:129) and 1,3-BP (dHBr: 3.07 Å and C-HBr: 138) leads to one dimensional
(1-D) chain along the c-axis (Figure 4.6). In addition to the C-HX interaction and
ππ stacking interaction, 1,3-XP revealed strong C-HO interaction between (1,3-FP:
dHO: 2.64 Å and C-HO: 156, 1,3-CP: dHO: 2.41 Å and C-HO: 149, 1,3-BP: dHO:
2.43 Å and C-HO: 162), carbonyl oxygen and pyrenyl hydrogen forming a 1-D chain
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A) B)
1,3-FP 1,8-FP
1,3-CP 1,8-CP
1,8-C’P
1,3-BP
1,3-IP 1,8-BP
-4.751e-2 4.751e-2
Figure 4.5. Calculated ESP maps of representative monomers of A) 1,3-XP and B) 1,8-XP
from crystal structure. All maps used consistent surface potential ranges [−4.75e-2 au (red) to
4.75e-2 au (blue)] and an isovalue of 0.000400 au.
along b, a, b, and a-axis respectively (Figures 4.6A,B,C&D). The C−HX and C-HO
intermolecular interactions act as steering for extending adjacent lamellae/columns
and generate a 3-D supramolecular assembly in the crystalline state. Intriguingly, in
1,3-IP, unusual Iπ interaction between iodine and π-electron cloud of neighboring
pyrene moiety mediated 1D- array was observed (dIπ: 3.67 Å) along the c-axis (Figure
4.6D). QTAIM analysis offered characteristic electron density (br0.066 eÅ-3; 7.38 kJ
mol-1) supporting the intermolecular interaction between the iodine moiety and π-
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A) B)
C(sp2)-HF
C(sp3)-HF
C-H  O
C-HO
C(sp2)-HCl
C(sp3)-HF & C(sp2)-HF
C) D)
C(sp3)-HBr
C-Iπ
C(sp3)-H I
ππ
C-H  O
C-H  O
Figure 4.6. Intermolecular interactions in 1,3-XPs. (A) intermolecular C-H•••F and C-H•••O
interactions in 1,3-FP; (B) C-H•••O and C-H•••Cl interactions in 1,3-CP; (C) C-H•••Br and
C-H•••O interactions in 1,3-BP and (D) C-H•••I, C-I•••π C-H•••O and ππ interactions in
1,3-IP.
electron cloud of neighboring pyrene moiety (Figure 4.7 and Table 4.3).
Analysis of the intermolecular contacts show that except 1,8-FP, all the other 1,8-
XP derivatives make ππ contacts and generate lamellar/columnar packing. In the
crystal packing of 1,8-FP, C−Hπ interactions (dHπ: 2.97 Å) involving C-H of pyrene
moiety with the π electron cloud of the neighboring pyrene moiety generate a
herringbone arrangement. The interplanar tilt angle between two neighboring pyrene
rings is 34° and the close intermolecular CC contacts are 3.5 Å. In addition, fluorine
moiety in 1,8-FP undergoes tetrafurcated interaction including (i) F interaction

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I5
C35
H13 H12
H18
H13 C36 I6
C21 C27
C29 C20 C19 H19
C18 H11
C22 C31 C17
C32
H14 C26
C23 C24 C25 C34 H22
C28
C30 C33
H15 H20
I2 H16 H17 H30 H29
H34
H28
H33 C48 C46 C45 C50
C55
C56 C39 H27
H3 H2 C51 C44
C38 C52 C43
H4 I1
C11 H23
C14 C4 C3 H1 H32 C40 C49 C42
C2 H10 C37 C47
C5 I4 H26
C6 C15 C1 C41
C7 C16 H31 H24 H25
H5 C54 C53
C8 C9 C12 C10
H6 C13
H7 H8 H9
I3
Figure 4.7. Shows QTAIM electron density map of 1,3-IP, arrows indicate the existence of
intermolecular I••• contacts.
(dFπ: 3.14 Å) between fluorine atom and π-orbitals of the C=O bond generating a
self-assembled dimer; (ii) two types of C-HF interactions between fluorine and
methylenyl hydrogens (dHF: 2.58 Å and 2.66 Å, C-HF: 111 and 106 respectively)
and (iii) C-FC interaction between fluorine and C of the alkyl group (dFC: 3.15 Å)
(Figure 4.8A). QTAIM analysis offered characteristic electron density (br0.05 eÅ-
Table 4.3. Calculated topological properties of the electron density for the intermolecular
interaction in XPs.
ad,  (r),
b b c 2b(r), DE,d
Interactions
(Å) (eÅ-3) (eÅ-5) (kJmol-1)
1,8-FP F1•••C38/F2•••C18 3.145 0.035 0.538 4.27
1,3-IP I2•••C21/I2•••C23 3.405 0.066 0.675 7.38
1,8-C’P H7•••H16/H8•••H15 2.165 0.042 0.504 4.25
H10•••H17/H9•••H18 2.389 0.035 0.469 3.71
1,8-BP H10•••H18/H9•••H17 2.524 0.029 0.418 3.30
Br2•••C20 3.476 0.039 0.446 3.43
ad=distance, bb(r)=electron density at the BCP, c2b(r)=Laplacian of
b(r) and dDE=dissociation energy.

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A) B) C(sp2)-HCl
C-FC=O C-Hπ
C-H  O
C(sp3)-HF
C(sp2)-HCl
C) D)
C-H  HC
C-H  HC
C-H  O
C-Brπ
Figure 4.8. Intermolecular interactions in 1,8-XPs. (A) intermolecular C-FC, C−Hπ and
C-HF interactions in 1,8-FP; (B) C-HCl and C-HO interactions in 1,8-CP; (C) C-
HH-C, and C-HO interactions in 1,8-CP and (D) C-HH-C and C-Brπ interactions
in 1,8-BP.
3; 4.26 kJ mol-1) supporting the intermolecular interaction between the fluorine and π-
orbitals of the C=O bond generating a self-assembled dimer (Figure 4.10 and Table 4.3).
In 1,8-CP, 1,8-CP and 1,8-BP, cofacial lamellar/columnar arrangement was observed
with strong ππ stacking interactions between neighboring pyrene units with an
3.56 Å 3.52 Å 3.44 Å
1,8-CP 1,8-CP 1,8-BP
Figure 4.9. Shows the decrease in the interplanar distance between pyrene units in 1,8-XP.
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interplanar distance of 3.56 Å (1,8-CP), 3.52 Å (1,8-CP) and 3.44 Å (1,8-BP) respectively
(Figure 4.9). Similar to 1,3-XP, a gradual decrease in the interplanar distance was
observed with increasing the polarizability of halogens. Detailed analysis of the single
crystal X-ray structure of 1,8-CP revealed the presence of two types of contacts
including C-HCl interaction and C-HO interaction which propagates the lamellar
arrangement in 3-D. Chlorine atom of one molecule undergoes trifurcated interaction
with two pyrenyl hydrogens (dHCl: 2.78 Å and 2.85 Å, C-HCl: 129 and 125
respectively) and pyrenyl carbon (dFπ: 3.45 Å) generating a 1-D array along b-axis.
The C-HO interaction mediated another 1-D array is generated along the a-axis
(dHO: 2.40 Å and C-HO: 144) (Figure 4.8B). In 1,8-CP, dihydrogen contacts between
two pyrenyl hydrogens with the distance of 2.16 Å plays a major role in extending the
columnar/lamellar arrangement in 2-D. Another 1-D array is generated along the a-
axis by the bifurcated interaction of the carbonyl oxygen with the hydrogen (dHO:
H32 H31
C59
C57 C56 H35
C51 C60
H4 H3 C50 C49
C58 C48
H25 C41 C55 C47
C42 C52 C46 H30
H2 H34
H5 H33
C5 C4 C44 C45 C54 H36
C12 C43 C53 H29
C13 H26
C3 H28
C6 H27
H6 H1
C15 C2 H21
C7 C16 H20 H19 H24
C8 C1
C40
C11 H10 C37 C39
H12 C14 C38 C30 C29
C17 H22 H23
C19 C9 C10 C31 C34
C20
C21 C28
H9 C18
H8 C36
H11 H7 C35 C27
C22 H18
H13 C26
C23
C32 C33
C24 C25
H17
H14
H15 H16
Figure 4.10. Shows QTAIM electron density map of 1,8-FP, arrows indicate the existence of
intermolecular C•••F interactions.

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2.63 Å and C-HO: 117) and carbon of the alkyl moiety with the distance of 3.17 Å
which further supports the stacking interaction (Figure 4.8C). In 1,8-BP, pyrenyl
dihydrogen interaction (dC–HH–C: 2.39 Å) mediated 1-D array was observed along the
c-axis. In addition, another 1-D array was observed along the a-axis via Br
interaction (dBrπ: 3.48 Å) (Figure 4.8D). These two interactions extend the lamellar
arrangement and generate a 3-D supramolecular assembly in the solid-state. QTAIM
H34
Cl6
A)
H33
H25
H9 Cl1
H22 H26
C18 Cl4 C42
H2 H10 C41 C43
C38
H13 H21 C51
H3 C52
H32 C55 H27
H14 C50
C2 C17
C3 C1 C44
C22 C37 H31 C49
C23 C21
H3 C12 C11 C45
C15 H15 C32 C56
H8 C31 C53
C4 C10 C35 C54 H28
H20
C5 C24 C30 C48 C46
C9 H7 C47
C16 C25 C29 H36
H4 C13 H29
C14 C36 H19
H16 C33
C6 C8 C34 Cl5 H30
C7 C26
C19 C28 H35
H5 H12 C27 H24
H17
H6 C39
C20
H18
Cl2 C40
H11
H23 Cl3
H3
H4
B) H2
H5 C12 C3 H12
C4 C2 Br1
H34 C5
C18
C1
C15 H11
O5 C58 Br5 C13 C17
H6
C11
H35 C6 C16
C57 O1
H33 C10
C7
H26 C9 H10
C8 C14
H32 C41
C50 C51 H7
C42 H9
C49
O6 C19 H17
C55 C43 H14 H18
C54
C20 C24 H16
H27
H36 C52 Br2 O2 C25
C59 C56 C32
C48 H19 C33
C44 H13 C26 C23
C60 H15
C47 H20 C36 Br3
Br6 C45 H28 C27 C35 C22
H37 C46 C53
C28 C31 C21
H31 H25
H23
C34
H29 C29 C30 C37 C38
H30 C40 C39
H24 H22 H23

Br4 H21 O3
O4
Figure 4.11. QTAIM electron density map of (A) 1,8-CP and (B) 1,8-BP indicating
intermolecular interactions.
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analysis further corroborate the dihydrogen contacts in 1,8-CP where C–HH–C
interaction (br0.04 eÅ-3; 4.25 kJ mol-1; Figure 4.11A, Table 4.3) aids in extending
linear arrangement of pyrene units along a-axis. In 1,8-BP, C–HH–C
(br0.090.05 eÅ-3; 3.30-3.71 kJ mol-1; Figure 4.11B, Table 4.3) contact promotes
orthogonal arrangement[201] of pyrene units along the c-axis. QTAIM calculations
also confirmed the existence of Br interactions in the crystalline 1,8-BP (br0.09
eÅ-3; 3.43 kJ mol-1), apart from the C–HH–C contacts (Figure 4.11B, Table 4.3).
Among the unusual interactions analyzed in XPs, I (DE=7.38 kJmol-1) represents
the strongest stabilizing interaction compared to F  (DE=4.27 kJ mol-1), Br
(DE=3.45 kJ mol-1) and dihydrogen contact (DE=3.30-3.71 kJ mol-1) (Table 4.3).
4.2.3. Hirshfeld surface analysis

Hirshfeld surface analysis[134] of the crystal structures of 1,3- and 1,8-XP give
insight into the nature of intermolecular interaction and packing motifs in the solid
2.6 2.6
CC CC 2.6 CC 2.6 CC

2.2 2.2
2.2 2.2
1.8 1.8
1.8 1.8
1.4 1.4
1.4 1.4
1.0 1.0 1.0 HBr 1.0
HH OH HH HCl
0.6 HF 0.6 OH HH HH OH HI
i i 0.6 OH 0.6
i
0.6 1.0 1.4 1.8 2.2 2.6 0.6 1.0 1.4 1.8 2.2 2.6 0.6 1.0 1.4 1.8 2.2 2.6 0.6 1.0 1.4 1.8 2.2 2.6
1,3-FP 1,3-CP 1,3-BP 1,3-IP
2.6 2.6 CC 2.6 CC 2.6 CC

2.2 2.2 2.2 2.2
1.8 1.8 1.8 1.8
1.4 1.4 1.4 1.4
1.0 1.0 1.0 1.0

HH CH HCl HBr
HF OH HH OH HCl OH HH OH
0.6 0.6 0.6 HH 0.6
i i
0.6 1.0 1.4 1.8 2.2 2.6 0.6 1.0 1.4 1.8 2.2 2.6 0.6 1.0 1.4 1.8 2.2 2.6 0.6 1.0 1.4 1.8 2.2 2.6
1,8-FP 1,8-CP 1,8-CP 1,8-BP
Figure 4.12. Hirshfeld 2D fingerprint plot of 1,3 and 1,8-XPs.

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Table 4.4. Shows the percentage of intermolecular contacts of a molecule in crystalline XPs.
CC HX OH CH HH CX CO a

1,3-FP 17.4 22.3 17.3 12.7 27.9 - - 0.73
1,3-CP 12.6 28.8 11.6 15.8 23.9 1.4 - 1.25
1,3-BP 16.7 30.1 13.2 9.4 25 - 3.2 0.56
1,3-IP 11.2 30 15.2 16.7 19.6 4.7 1.6 1.49
1,8-FP 6 21.2 17.8 28.8 20.6 1.8 - 4.8
1,8-CP 9.4 24.4 15.7 21.1 21 4 2.3 2.24
1,8-
13.4 26.1 14.3 14.4 25.1 1.2 1.7 1.07
CP
1,8-BP 13.5 29.5 15.5 16.4 20.7 2.8 0.7 1.21
a(%𝐶𝐻)⁄(%𝐶𝐶);Herringbone4.5Sandwichherringbone.4.0Lamellar.
.7Columnar 0.46.0[30].
state (Figure 4.12). Table 4.4 contains the percentages of contributions for various
contacts in XPs. It is evident from the table that HH, OH, HX, CC and CH
interactions in XP can account for more than 90% of the Hirshfeld surface area (97.6%
in 1,3-FP, 92.7 % in 1,3-CP, 94.4 % in 1,3-BP, 92.7 % in 1,3-IP, 94.4 % 1,8-FP, 91.6 % in
1,8-CP, 93.3 % in 1,8-CP and 95.6 % in 1,8-BP). In the 2D fingerprint plots, two sharp
spikes of almost equal length are characteristic of C−HO interactions. The central
spikes extending to (di, de) region of (1.2Å, 1.2Å) in 1,3-XP reveal relatively high
percentages of HH contacts whereas the central spike corresponding to HH
interaction of 1,8-XP extend up to (di , de) region of (1.3 Å, 1.3 Å) in 1,8-FP, (1.2 Å, 1.2
Å) in 1,8-CP, (1 Å, 1Å) in 1,8-CP and (1.1 Å, 1.1Å) in 1,8- BP. The sharpness of central
spike in 1,8- is a consequence of close HH contacts (∼2.16 Å) in CP that can be seen
in the Hirshfeld surface as bright red spots. A significant C−Hπ interaction has been
observed for 1,8-FP as indicated by the wings in the upper left and lower right of the
2D fingerprint plot extending up to (di, de) region of (1.7 Å, 1.7 Å) and contributes
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28.8 % of the total contacts. It can be seen that the CC contacts, associated with ππ
stacking interactions in the (di, de) ≈ 1.8 Å, 1.8 Å) region, are strong for XPs except 1,8-
FP where it is minimal (only 6 % of the surface is due to CC interactions) suggesting
minimum ππ stacking interactions. Occurrence of such weak intermolecular
interactions dictates the molecular packing that results in ideal face-to-face columnar
1-D π stacks (β- motif) in 1,3-FP ( = 0.73), 1,3-BP ( = 0.56) and 1,8-CP ( = 1.07)
whereas the values suggest face-to-face lamellar 1D π stacking arrangement (γ-
motif) in 1,3-CP ( = 1.25), 1,3-IP ( = 1.49), 1,8-CP ( = 2.24) and 1,8-BP ( = 1.21) . A
value of  = 4.8 in 1,8-FP indicates the formation of edge-to-face herringbone
arrangement in the crystalline lattice when compared to other XPs[30]. Thus, we have
realized the switching of sandwich herringbone to lamellar/columnar arrangement by
introducing -haloacetyl substituents in pyrene.
High transportation capabilities of charge carriers in pyrene based
semiconductors has attracted its application in p-type and ambipolar OFETs[16-17].
The recent interests in pyrene based semiconductors is due to control over molecular
architecture that can be achieved by modifying the structure by varying the position
of substitution on the pyrene ring. Herein, we report on comparative investigation of
conductivity in systematically synthesized acetylpyrene (AP) derivatives. In our
approach, we first study the morphology of the derivatives by scanning electron
microscopy (SEM), atomic force microscopy (AFM), and tunneling electron
microscopy (TEM). Further, we determine the I-V profiles of the derivatives and use
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field-effect transistor (FET) measurements to obtain the charge carrier mobility which
corroborate with theoretically predicted trend.
Previously, we reported the synthesis of acetyl pyrenes derivatives (1-4AP) by
treating a required amount of acetyl chloride to a solution of pyrene in carbon
disulphide (Figure 4.13, Row I). The derivatives were analytically and spectroscopy
characterized along with the X-ray molecular structure. Acetyl derivatives (1, 2’, 2”, 3,
4AP) exhibit a monoclinic system, a crystal system described by vectors of unequal
lengths, while 2AP exhibits an orthorhombic system (Figure 4.13, Row II). The
derivatives 1AP and 2’AP tend to crystallize following a herringbone pattern, wherein
the molecules interact face-to-edge through C-H•••π interactions and minimize the

II
II
Herringbone Sandwichherringbone Brickwork -Lamellar/Columnar

(>4.5) (3.2<<4.5)  (1.2<<2.7) (0.46<<1.0)
Figure 4.13. Row I: chemical structure of 1–4 AP; Row II: stereo microscopic images of
corresponding single crystal and Row III: schematic drawing that depicts the possible crystal
packing pattern and the range of = (%CH)/(%CC) contact ratio for each packing.
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electrostatic π-orbital repulsion (Figure 4.13, Row III). A similar crystallographic
analysis on 2AP and 2”AP classify the crystallization pattern to be brickwork, which
is very promising for high charge carrier mobility and less sensitive to charge traps
(Figure 4.13, Row III). 3AP and 4AP has completely planar geometry where the torsion
angle between the pyrene rings is 0. The molecules 3AP and 4AP form a unique two-
dimensional columnar structure, wherein the molecules stack with a short
intermolecular separation of 3.4–3.5 Å (Figure 4.13, Row III).
4.2.4. Morphological Analysis
Effect on increasing the acetyl group substitutions on pyrene unit brings
different morphological characterization on the self-assembly of AP derivatives. These
morphologies in aggregate were extensively studied by a variety of microscopic
including SEM, AFM and laser scanning confocal microscopy. SEM images of the
molecular aggregate in 1AP, drop-casted in benzene solution on silicon wafer, reveals
A) B) C)
10 m 10 m 10 m
D) E) F)
20 m 10 m 3 m
Figure 4.14. SEM images of A) 1AP B) 2AP C) 2’AP D) 2”AP E) 3AP and F) 4AP, drop
casted in benzene.
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nearly mono dispersed micro spheres, with an average diameter of 8.17 mm (Figure
4.14A). The spherical morphology of molecular aggregate strongly attributes to the it
has a herringbone packing. The micro wires have average width of 1.05 m and
average length of 43.59 m which corresponds to an aspect ratio of 41.24 herringbone
packing (absence of  stacking) which prevents one dimensional assembly of the
molecules. The formation of micro wires of low aspect ratio in 2’AP may be due to
increased CH•••O interaction between the adjacent molecules, though (Figure 4.14C).
Favourable  stacking of pyrene core in 2AP and 2’’AP shows a lamellar molecular
assembly resulting in micro belts (Figure 4.14B&D) with an average width of 2.40 m
and 7.72 m respectively. These micro belts are few tens of micrometre in length, as
evident from the laser confocal imaging (which is discussed latter) which leads to high
aspect ratio. This high aspect ratio accounts for more organized molecular stacking
and one dimensional extended growth along the long axis in the belts. Increased
CH•••O interaction in 3AP and 4AP induces co-planarity in the pyrene units which
in turn promotes  stacking that leads to the formation of long single crystalline
self-assembled micro structures (Figure 4.14E&F).
AFM image of AP derivatives in benzene drop-casted on mica sheet captures
the cross-sectional width and height of the distinct morphology of the self-assembly.
The self-assembled structures so formed are in good agreement with SEM data. The
morphology of 1AP was resolved for small sphere like assembly with a cross-sectional
height of 1.67 nm (Figure 4.15A). In 2AP and 2’’AP, a cross section perpendicular to
the axis of the belts shows an average belt height of about 286.11 nm and 268.55 nm
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A) C) B)
0 1: Height 742.2 nm 0 1: Height 20 m 0 1: Height 15 m
D) E) F)
1: Height 1: Height 8 m0 1: Height 6.2 m

0 20 m 0
Figure 4.15. Show the AFM images of A) 1AP; B) 2AP; C) 2’AP; D) 2”AP; E) 3AP and F)
4AP, drop casted in benzene.
respectively (Figure 4.15B&D). Detailed examination of these micro belts along their
length reveals that they are uniform in cross-sectional width of 1.47 m and 2.37 m
respectively which corroborate with the SEM analysis.
The role of substrate were again nullified when silicon wafer and mica sheet used
for SEM and AFM respectively, was replaced with glass coverslips to investigate the
laser confocal imaging in order to understand the surface assisted self-assembling of
AP derivatives. Confocal imaging of the molecular assembly of 1AP drop-casted on
glass coverslips showed particulate aggregate in an approximately spherical shape,
with average size of 2.50 m (Figure 4.16A). The spherical morphology of molecular
aggregate is consistent with the distorted  stacking which is in good accord with
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A) B) C)
20 m 20 m 30 m
D) E) F)
200 m 30 m 30 m
Figure 4.16. Show the laser confocal images of A) 1AP; B) 2AP; C) 2’AP; D) 2”AP E) 3AP
and F) 4AP, drop casted in benzene.
the SEM and AFM data. The establishment of herringbone packing in 2’AP were
identified through the formation of low aspect ratio micro wires of having an average
width of 2 m and average length of 30 m (Figure 4.16C). The characteristic flat
morphological feature remained unperturbed in drop-casted 2AP and 2’’AP though
the formation of microstructures with high aspect ratio (Figure 4.16B&D). The self-
assembled microstructures forms fairly uniform microbelts with length ranging from
tens to hundreds of micrometres. The morphology of self-assembled structures
attained in 3AP and 4AP, leads to the formation of microfibril, consistent with the
extended molecular stacking within the long microfibrils determined by the collective
interaction between the large numbers of co-facially stacked pyrene units (Figure
4.16E&F). As revealed through the SEM analysis, 3AP and 4AP were composed of
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microsized fibrils with high aspect ratio. The extended 1D self-assembly is likely
dominated by the strong  interaction between the pyrene scaffolds, as indicated
by the X-ray diffraction, for which the typical  stacking of 3.57 and 3.45 Å was
observed respectively.
To further correlate the observed morphology of the molecular self-organization
of AP derivatives with the crystal structure, we performed electron diffraction studies
by drop-casting on carbon (copper grid; Figure 4.17). Bright filed transition electron
microscopy (TEM) observations, demonstrate that 1AP ends up in highly dispersed
micro spherical aggregates which corroborates with the SEM analysis. While 2AP,
2’’AP, 3AP and 4AP exhibits high aspect ratio self-assembled structures, ensuring the
involvement in  stacking along different axis.
Figure 4.17. Show the TEM images of a) 1AP; b) 2AP; c) 2’AP; d) 2”AP; e) 3AP and f) 4AP,
drop casted in benzene.

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4.2.5. Conductivity measurements and theoretical calculations
To evaluate the intrinsic molecular packing on charge-transport properties,
microcrystals suitable for device fabrication were prepared through drop-casting AP
derivatives in benzene (1 mM) on a glass slide (1 cm×1 cm). The current-voltage (I–V)
characteristics were investigated by two probe method by scanning the voltage from
0 to 10 V with a sweeping rate of 1.0 V s−1 (Figure 4.18A). The linear dependence of the
applied voltage under positive biases suggests an Ohmic carrier-transporting process
inside the organic semiconductor. Under similar conditions, for the given area on the
glass slide (1 cm×1 cm) and the concentration of the sample (AP) drop-casted (1mM),
we extracted the electrical resistance (R) for the drop casted samples. The slope
calculated from the linear fit of the I-V characteristics for the applied positive bias
voltage range gave the resistance for the drop casted samples. A high resistance was
offered to the charge transfer in 1AP (847 M) and 2’AP (332 M) while 2AP (21 M),
Figure 4.18. I-V profile determination by A) drop-casting in benzene; B) single crystal and C)
single crystal organic field-effect transistor (OFET) measurement on 4AP.

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2’’AP (18 M), 3AP (77 M) and 4AP (27 M) allows an easy accessibility to the
charge transfer. The crystal structural analysis of 1AP and 2’AP affords the packing of
pyrene units in so called herringbone packing in which the molecules are packed
through edge-to-face in two-dimensional. This adverse edge-to-face packing of
pyrene units minimize the  between the adjacent molecules while the stacked face-
to-face observed in brickwork (2AP and 2’’AP) and columnar (3AP and 4AP) lead to
higher charge transfer. Hence the observed decrease by an order of one magnitude in
the resistance seems that the crystals with -stacked packing (brickwork and
columnar) better than those with herringbone packing. The unsubstituted pyrene (P)
showed a high resistance in magnitude of giga ohms.
To establish a direct correlation between solid-state packing and charge
transport properties, we measured the resistance through the single crystals which
allows us to study the corresponding electrical resistivity properties (). By taking
representative examples from herringbone, brickwork and columnar, illustrated
through the crystal packing in 1AP, 2AP and 4AP respectively we demonstrated the
relationship of charge transport properties and the packing modes of single crystals.
We observed a linear relationship for the current-voltage (I-V) characteristics
measured for bias voltages in the range of 0 V to 10 V (Figure 4.18B). The electrical
resistance (R) for 1AP was calculated from the slope of linear plot of I-V to be R 3.29×
109 . By measuring the dimension of the singe crystal (1AP) of length (L) 122 mm
and area cross-section (A), ≈ calculated as 218.22 m (width) × 250 m (height), we can
determine the single crystal resistivity R A/L 1.89×107 m. Similarly the
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resistivity () for 2AP and 4AP were calculated as 1.25×104 m and 0.72×104 m
respectively. The comparison of resistivity between 1AP crystal with 2AP and 4AP
indicates that the charge transporting ability differ by three order, suggesting that the
two dimensional orbital overlap in brickwork (2AP) and columnar (4AP) are more
effective for carrier transport than herringbone (1AP) packing.
Having successfully investigated the effect of molecular packing in single
crystals on charge transport, we further explored the mobility measurement on single-
crystal transistors on 4AP. Single crystal FETs (SC-FETs) were fabricated using the
top-contact, bottom-gate geometry on highly doped p-type silicon wafers with 300 nm
thick thermally grown silica as the gate dielectric material. Figure 4.18C shows drain
current (IDS) vs. source voltage (VDS) for various gate voltage (VG). The inset gives the
transfer characteristics IDS vs VG at VDS = 20 V. In both the output and transfer
characteristics, the drain current is found to increase at negative gate voltages due to
injection of holes in the conduction channel confirming p-channel electrical
characteristics of the single-crystal device. The linear nature of the output
characteristics assures that a good Ohmic contact with the gold electrode has been
achieved. Since the device operation is in the linear regime, we have used the
following equation in the calculations;
𝐼𝐷𝑆 = (𝑊/𝐿)𝜇𝐶𝑖 (𝑉𝐺 − 𝑉𝑇 )𝑉𝐷𝑆
where W = 10 µm and L= 60 µm are the width and the length of the channel and C i=
11.5 nF/cm2 is the gate capacitance per unit area. The hole mobility is extracted for
various gate voltage by calculating ∂IDS∂VG in the IDS versus VG plot. At increasingly
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negative gate voltages, the mobility was found to monotonously increase from 0.03 to
0.18 cm2 V-1 s-1, a value which is in good agreement with the theoretically predicted
value of 0.2 cm2 V-1 s-1.
4.3. Conclusion
A series of -haloacetyl pyrene derivatives are reported and the effect of halogen
interaction and dihydrogen contacts in bringing lamellar and columnar arrangement
of pyrene is evaluated in the crystalline state. Incorporation of -haloacetyl group to
pyrene skeleton switched the sandwich herringbone to lamellar/columnar packing
motifs. High degree of control over the π-stacking through the strategy of tuning the
charge distribution by the incorporation of different halogen atom decreased the
interplanar distances between pyrene moieties from 3.52 Å in 1,3-FP to 3.49 Å in 1,3-
IP and 3.58 Å in 1,8-CP to 3.44 Å in 1,8-BP in lamellar/columnar motifs. QTAIM
analysis confirmed the homopolar dihydrogen contacts in 1,8-CP/BP where the
accumulation of electron density promotes linear arrangement of pyrene units in 1,8-
CP while orthogonal arrangement in 1,8-BP. Apart from the dihydrogen contacts and
hydrogen bonding, halogen interactions including Br and Iinteraction play
pivotal role in extending the columnar/lamellar arrangement in a 3D manner.
Hirshfeld surface analysis displayed (%CH)/(%CC)] values suggesting the
increased face-to-face lamellar/columnar arrangement in the crystalline -haloacetyl
pyrenes. This strong tendency to form self-assembled, well-defined
lamellar/coloumnar stacks marks a-haloacetyl pyrene as promising candidates

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application in opto-electronic devices.
High charge mobility was observed in single crystalline brickwork/ columnar (2
and 2’’AP/ 3 and 4AP) when compared to the herringbone structure (1AP) suggesting
that the two dimensional orbital overlap are more effective for carrier transport. These
findings reveal the control over morphology that can be achieved in acetylpyrene to
form microscale conducting materials. The OFET devices fabricated with single
crystals of 4AP, displayed the hole mobility of 0.18 cm2 V-1 s-1, a value which is in good
agreement with the theoretically predicted value of 0.2 cm2 V-1 s-1.
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4.4. Appendix
All chemicals were obtained from commercial suppliers and used as received
without further purification. All reactions were carried out in oven-dried glassware
prior to use and wherever necessary, were performed under dry nitrogen in dried,
anhydrous solvents using standard gastight syringes, cannulae, and septa. Solvents
were dried and distilled by standard procedures. TLC analysis were performed on
precoated aluminum plates of silica gel 60 F254 plates (0.25 mm, Merck) and
developed TLC plates were visualized under short and long wavelength UV lamps.
Flash column chromatography was performed using silica gel of 200-400 mesh
employing a solvent polarity correlated with the TLC mobility observed for the
substance of interest.
X-ray Crystallography
The single crystal X-ray (SC-XRD) method is discussed in Chapter 2 (Appendix 2.)
Computational methods
Quantum Theory of Atoms in Molecules (QTAIM): The wave function for XPs were
obtained employing the geometries taken from the crystal structure using Gaussian
set of codes at B3LYP/6-311G**++ level.1 Quantum theory of atoms in molecules
(QTAIM) analysis helps to understand the description of interatomic interaction in the
single crystal X-ray structure. A bond is defined along the bond line between two
nuclei, called a bond path, along which electron density is concentrated. The bond
critical point (BCP) is a point along the bond path at the interatomic surface, where
the shared electron density reaches a minimum. The physical characteristics of the
BCPs [the electron density at BCP, (rBCP), and its Laplacian, 2(rBCP)] reveal the
approximate measure of the amount of electron density built up in the bonding region
and as such could be taken as characteristic of the bond. When 2(rBCP) < 0 and is
large in magnitude, (rBCP) is also large which means that there is a concentration of
transistors
electronic charge in the internuclear region. This is also an indication of a sharing of
electronic charge between both nuclei that defines the covalent (polar) bond. When
2(rBCP) < 0 there is a depletion of electronic charge in the internuclear region. Using
the AIM 2000 software package, the electron density was integrated over atomic
basins according to the quantum theory of atoms in molecules using PROAIM, and
thus the BCP data and the molecular graphs were obtained.
Hirshfeld analysis: Important intermolecular interactions within the crystal structure
of XPs were identified through Hirshfeld surface analysis using Crystal Explorer 3.1.
The Hirshfeld surface is defined as a set of points in 3D space where the ratio of
promolecule and procrystal electron densities is equal to 0.5. The exploration of
intermolecular contacts is provided by mapping normalized contact distances (dnorm),
which is a function of a closest distance from the point to the nuclei interior (d i) and
exterior (de) to the surface as well as on the van der Waals radii (rvdw). 2D fingerprint
which were generated by deriving from the Hirshfeld surface by plotting the fraction
of points on the surface as the fuction of di and de which provide a visual summary of
intermolecular contacts within the crystal.
Electrostatic surface potential: Electrostatic surface potential map illustrate the
charge distributions of molecules three dimensionally. These maps allow us to
visualize variably charged regions of a molecule. Knowledge of the charge
distributions can be used to determine how molecules interact with one another.
Gaussian supports the cube keyword to generate the cubes separately from the
formatted checkpoint file using the cubegen utility program. This allows for the
generation of electrostatic surface potential mapping of the molecule.
Schrödinger materials science suite: Theoretical calculations of charge carrier
mobility were performed on the crystal structures in Schrödinger Materials Science
Suite 2015-1 using Jaguar DFT engine. The hopping model was used for the
predictions of charge carrier mobility. Geometry optimization and single point energy
calculations of monomer for neutral ground state and radical ions were performed at
B3LYP/LACVP**+ level of theory. Same level of theory was used for cluster
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calculations. Electron reorganization energy (λe) and hole reorganization energy (λh)
were calculated using the adiabatic potential energy surfaces method. To compute
charge carrier transfer rates, spherical nanoparticle clusters of 10Å were built for 1-
4AP using the Nanoparticle builder in Schrödinger Materials Science Suite. The
packing was carefully visualized to select only the immediate neighbor of the chosen
central molecule. Average charge carrier mobility rates were determine using Marcus
theory, while ignoring the anisotropy effects.
Atomic force microscopy (AFM): AFM analyses were carried out on multimode
scanning probe microscope (Veeco Nanoscope V, digital instruments). Samples for
analyses were prepared by drop casting 1mM solutions of the samples (1-4AP) in
benzene on a freshly cleaved mica surface and dried under air. To exclude any
artefacts, blank experiments were performed with solvent alone evaporated on mica.
Imaging was done under ambient conditions in tapping mode regime. Micro-
fabricated antimony doped silicon cantilever (MPP-11100-10, resonance frequency-
279–379 KHz, spring constant- 20–80 Nm-1) tip was used to probe the sample surface.
The scan rates were varied from 0.5 Hz to 1.5 Hz and AFM section analyses were
carried out offline. The average dimension of the selfassembly of 1-4AP were
estimated from the Lorentzian fit of the histogram of the particle size distribution
curves obtained after correcting for the tip-broadening effect.
Transmission electron microscopy (TEM): TEM measurements were carried out on
FEI Tecnai 30 G2 high resolution transmission electron microscope and JEOL 2010
with an accelerating voltage of 100 kV. The samples were prepared by drop casting
1mM 1-4AP in benzene solution of on a 400 mesh carbon-coated copper grid (Ted
Pella, Inc.) at ambient conditions and allowing the excess solvent to evaporate under
air in dust free conditions. TEM images were obtained without staining. The average
dimension of the self-assembly of 1-4AP were estimated from the Lorentzian fit of the
histogram of the particle size distribution curves
Scanning electron microscopy (SEM): FE-SEM measurements of NIN was carried out
on FEI Nova NanoSEM 450 (FEG type), drop casting 1 mM 1-4AP in benzene on silicon
transistors
wafer and allowing to evaporate the excess solvent under air in dust free conditions.
The sample was further subjected to thin chromium sputtering using JEOL JFC-1100
fine coater to increase the signal/noise ratio. The probing side was inserted into JEOL
JSM-5600 LV scanning electron microscope for obtaining the images. The average
diameter of the particles was determined from the Lorentzian fit of the size
distribution curve.
Confocal optical microscopy: Fluorescent microscopic images of the 1-4AP sample
was obtained from inverted optical microscope (LeicaSP5-DMRX Optical Microscope)
equipped with a wide range of objective lenses, the sample was excited under the
illumination of UV light (ex= 405 nm, continuous laser, ≥ 10 mW, pulse width < 100
ps) and the emission was monitored at 480 nm. The samples (1 mM AP in benzene)
were drop casted on a freshly cleaned glass coverslip, and allowed to dry under air.
The coverslip was sealed on a glass slide avoiding the air bubbles and kept
undisturbed. Further, slides were imaged at 63X magnification in the presence of
immersion oil.
Device Fabrication:
a) I-V measurenment on drop-cased sample: I-V measurements were carried out by
drop-casting the solution of 1-4AP in benzene (1ml of 1mM solution) on a glass
slide of dimension 1x1cm. Once the solution on the glass is dry, silver paint is put
at the edge of the glass plate to connect the copper wire and the crystals.
b) I-V measurenment on single crystal: The crystals 1AP, 2AP and 2’AP are
reasonably large about 3-4mm were selected and arranged on a glass substrate and
conductive silver paint was used to put electrical contact on the crystal and the
copper wire. The measurement setup included a voltage source which is supplied
to the device under test. The current is measured through a preamplifier to Digital
Multimeter.
c) FET measurement on single crystalline 4AP: For field-effect mobility
measurements, high-purity single crystals of 4AP were grown from solution. Single
crystal FETs (SC-FETs) were fabricated using the top-contact, bottom-gate

transistors
geometry on highly doped p-type silicon wafers with 300 nm thick thermally
grown silica as the gate dielectric material. Gold electrodes were thermally
evaporated with a shadow mask for the channel. For surface functionalization,
benzyl mercaptan was drop-casted before placing the crystal. It should be noted
that the thiol was found to enhance the conduction of these SC-FETs by almost two
orders of magnitude but by itself plays negligible role in the transfer characteristics.
The 4AP crystals on average were 600 µm along a-axis and 15 µm along b-axis,
giving the device W/L ratio of around 0.25.
Synthesis Details
The synthesis, purification and characterization of 1,3- and 1,8-Bis(acetyl)pyrenes
(1,3-AP and 1,8-AP) were reported in Chapter 2 (Appendix 2.5).
Scheme 4.1. Synthesis of 1,3- and 1,8-Bis(chloroacetyl)pyrene (1,3-CP and 1,8-CP).
Synthesis of 1,3- and 1,8-Bis(chloroacetyl)pyrene (1,3-CP and 1,8-CP): Pyrene (1.0 g;
4.9 mmol) dissolved in CS2 (yellow solution; 250 mL) was cooled to 0 °C (ice bath) and
subsequently anhydrous AlCl3 was added. Chloroacetyl chloride (2.49 g; 0.198 mols)
was then syringed slowly to the suspension and the ice bath was removed. Hydrogen
chloride was liberated upon warming to room temperature. After 3 h, the mixture was
added slowly to a vigorously stirred mixture of ice and concentrated HCl. The
resulting suspension was filtered and vacuum dried and further purified by column
chromatography (chloroform:hexane 1:2) to give Bis(chloroacetyl)pyrene.
1,3-CP (yield= 32.8%) M.p. 143-146 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 9.09 (s, 1H),
8.69 (d, J = 9.35 Hz, 2H), 8.49 (d, J = 8.05 Hz, 2H), 8.46 (d, J = 8.05 Hz, 2H), 8.26 (m, 1H),
5.07 (s, 4H). 13C NMR [125 MHz, DMSO(d6), δ]: 192.21, 131.54, 131.12, 130.15, 129.28,
transistors
128.73, 128.27, 127.78, 124.55, 124.31, 123.52, 32.04. IR (KBr, cm-1) 3027.51, 2945.30,
1595.13, 1690.21, 850.61. Elemental analysis: calcd. value for C20H12Cl2O2: 67.63% C,
3.41% H; found: 67.98% C, 3.61% H. HRMS (EI) m/z calculated for C20H12Cl2O2 [M]+:
354.0214, found: 354.0298.
1,8-CP (yield= 37.5%) M.p. 155-158 °C. 1H NMR [500 MHz, DMSO (d6), δ]: 8.65 (s, 2H)
8.54 (d, J = 7.5, 2H), , 8.32 (d, J = 3 Hz, 2H), 8.09 (s, 2H), 5.07 (s, 4H). 13C NMR [125 MHz,
DMSO (d6), δ]: 197.82, 134.25, 130.63, 129.43, 129.36, 128.57, 127.54, 126.14, 125.14,
38.18. IR (KBr, cm-1) 3057.54, 2965.31, 1587.13, 1692.51, 852.56. Elemental analysis:
calcd. value for C20H12Cl2O2: 67.63% C, 3.41% H; found: 67.88% C, 3.48% H. HRMS (EI)
m/z calculated for C20H12Cl2O2 [M]+: 354.0214, found: 354.0292.
Scheme 4.2. Synthesis of 1,3- and 1,8-Bis(bromoacetyl)pyrene (1,3-BP and 1,8-BP).
Synthesis of 1,3- and 1,8-Bis(bromoacetyl)pyrene (1,3-BP and 1,8-BP): A solution of
acetylpyrene (AP) (1.0 g; 5 mmol) in EtOAc (20 mL) and CHC13 (20 mL) was heated
to reflux with finely powdered CuBr2 with vigorous stirring for 3.5 h. The yellow
precipitate was filtered off, washed with CH2Cl2, dried, and combined with the
residue obtained from evaporation of the filtrate. This material was extracted with
boiling benzene (5×125 mL), filtered and concentrated and further purified through
column chromatography (1,3-BP, chloroform:hexane 1:2 and 1,8-BP
chloroform:hexane 1:1).
1,3-BP (yield= 66%). M.p. 158-161 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 9.16 (s, 1H),
transistors
128.53, 128.07, 127.87, 124.95, 124.31, 123.42, 31.14. IR (KBr, cm-1): 3095.75, 2920.23,
1664.57, 862.18. Elemental analysis: calcd. value for C20H12Br2O2: 54.08% C, 2.72% H;
found: 54.32% C, 2.77% H. HRMS (EI) m/z calculated for C20H12Br2O2 [M]+: 441.9204,
found: 441.9230.
1,8-BP (yield= 83%). M.p. 193.5-195.0 C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.76 (s,
2H), 8.64 (d, J = 8.05 Hz, 2H), 8.44 (d, J = 8.05 Hz, 2H), 8.33 (s, 2H), 5.14 (s, 4H). 13C
NMR [125 MHz, DMSO, δ]: 195.60, 134.07, 130.66, 129.99, 128.72, 128.18, 126.88, 126.43,
124.11, 37.46. IR (KBr, cm-1): 3095.75, 2978.09, 1664.57, 1506.41, 860.25. Elemental
analysis: calcd. value for C20H12Br2O2: 54.08% C, 2.72% H; found: 54.25% C, 2.88% H.
HRMS (EI) m/z calculated for C20H12Br2O2 [M]+: 441.9204, found: 441.9223.
Scheme 4.3. Synthesis of 1,3- and 1,8-Bis(fluroacetyl)pyrene (1,3-FP and 1,8-FP).
Synthesis of 1,3- and 1,8-Bis(fluoroacetyl)pyrene (1,3- and 1,8-FP): CsF (515.51 mg;
3.39 mmol) was added to a mixture of bromoacetylpyrene (BP) (250 mg; 0.57 mmol),
pentaEG (119 mg; 0.5 mmol), and MeCN (4 mL) in a vial. The mixture was heated for
1.5 h at 100 °C. The reaction time was determined by checking TLC. The mixture was
filtered and washed with Et2O, and the filtrate was evaporated under reduced
pressure. Column chromatography on silica gel (10% EtOAc/hexane) afforded 195 mg.
1,3-FP (yield= 7%). M.p. 133-135 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 9.10 (s, 1H),
128.43, 128.05, 127.78, 125.05, 124.45, 123.76, 31.45. IR (KBr, cm-1): 3105.7, 2987.4, 1662.0,
956.6. Elemental analysis: calcd. value for C20H12F2O2: 74.53% C, 3.75% H; found:
transistors
74.65% C, 3.82% H. HRMS (EI) m/z calculated for C20H12F2O2 [M]+: 322.0805, found:
322.0856.
1,8-FP (yield= 10%). M.p. 193.5-195.0 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.57 (s,
2H), 8.55 (d, J = 8.05 Hz, 2H), 8.37 (d, J = 8.05 Hz, 2H), 8.28 (s, 2H), 5.24 (s, 4H). 13C
NMR [125 MHz, DMSO, δ]: 194.70, 133.98, 131.06, 129.57, 128.52, 128.08, 126.78, 126.33,
124.23, 36.86. IR (KBr, cm-1): 3112.0, 2995.1, 1662.3, 966.2. Elemental analysis: calcd.
value for C20H12F2O2: 74.53% C, 3.75% H; found: 74.72% C, 3.62% H. HRMS (EI) m/z
calculated for C20H12F2O2 [M]+: 322.0805, found: 322.0892.
Scheme 4.4. Synthesis of 1,3- and 1,8-Bis(iodoacetyl)pyrene (1,3- and 1,8-IP).
Synthesis of 1,3- and 1,8-Bis(iodoacetyl)pyrene (1,3- and 1,8-IP): Finely powdered
CuO (0.40 g; 5.0 mmol) and I2 (1.27 g; 5.0 mmol) were added to a well-stirred solution
of the acetylpyrene (AP) (5.0 mmol) in anhyd. methanol (20 mL). The mixture was
stirred for 5 min and then refluxed. After disappearance of the reactant (1–12 h,
monitored by TLC), the mixture was filtered and the solvent was removed under
reduced pressure. The residue was poured into 10% Na2S2O3 solution (50 mL), the
mixture was extracted with EtOAc (3×30 mL), and the organic layer was dried
(Na2SO4). Removal of the solvent and purification of the residue by column
chromatography yielded 1,3- (chloroform) and 1,8-IP (chloroform:hexane 1:1).
1,3-IP (yield= 65.0%) M.p. 178-181 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 9.21 (s, 1H),
128.73, 128.01, 127.95, 125.01, 124.25, 123.65, 30.45. IR (KBr, cm-1) 3039.33, 2977.61,
transistors
1650.58, 1251.32, 594.08. Elemental analysis: calcd. value for C20H12I2O2: 44.64% C,
2.25% H; found: 44.94% C, 2.52% H. HRMS (EI) m/z calculated for C20H12I2O2 [M]+:
537.8927, found: 537.8979.
1,8-IP (yield= 37.5%) M.p. 155-158 °C. 1H NMR [500 MHz, DMSO(d6), δ]: 8.69 (s, 2H),
8.63 (d, J = 9.35 Hz, 2H), 8.42 (d, J = 8.05 Hz, 2H), 8.31 (s, 2H), 5.14 (s, 4H). 13C NMR
[125 MHz, DMSO (d6), δ]: 196.60, 134.11, 130.95, 129.67, 128.57, 128.09, 126.79, 126.60,
125.01, 37.59. IR (KBr, cm-1) 31341.3, 2898.6, 1668.6, 1240.9, 591.9. Elemental analysis:
calcd. value for C20H12I2O2: 44.64% C, 2.25% H; found: 44.89% C, 2.62% H. HRMS (EI)
m/z calculated for C20H12I2O2 [M]+: 537.8927, found: 537.8990

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List of publications 190
List of publications
1. Haloacetylation Driven Transformation Haloacetylation Driven Transformation of
Herringbone to Lamellar/Columnar Packing in Pyrene
Salini P. S.; † Rajagopal, S. K.;† Hariharan, M*
Cryst. Growth Des. [10.1021/acs.cgd.6b00919].
2. S,  and C-H Contacts Regulate Solid-State Fluorescence in Regioisomeric
Bisthiazolylpyrenes
Rajagopal, S. K.; Salini P. S.; Hariharan, M*
Cryst. Growth Des. 2016, 16, 4567-4573 (Most Read Article).
3. Crystallization Induced Green-Yellow-Orange Emitters Based on Benzoylpyrenes
Rajagopal, S. K.; Reddy, V. S.; Hariharan, M*
CrystEngComm. 2016, 18, 5089-5094 (Outside Frontispiece).
4. Progressive Acylation of Pyrene Engineers Solid State Packing and Colour via C-HH-C,
C-HO and  Interactions
Rajagopal, S. K.; Philip, A. M.; Nagarajan, K.; Hariharan, M*
Chem. Commun. 2014, 50, 8644-8647. (Inside Frontispiece).
5. C-HH-C and C-H Contacts Aid Transformation of Dimeric to Monomeric
Anthracene in the Solid State
Nagarajan, K.; Rajagopal, S. K.; Hariharan, M*
CrystEngComm. 2014, 16, 8946-8949.
6. Non-Natural G-quadruplex in a Non-Natural Environment
Rajagopal, S. K.; Hariharan, M*
Photochem. Photobiol. Sci. 2014, 16, 8946-8949.
7. DNA-Enforced Conformational Restriction of an Atropisomer
Cheriya, R. T.; Joy, J.; Rajagopal, S. K.; Nagarajan, K.; Hariharan, M*
J. Phy. Chem. C 2012, 116, 22631-22636.
(†Both the authors contributed equally)

Presentations and Conferences 191
Presentations and Conferences

• Received best poster presentation award in 5th Inter-IISER Chemistry Meet 2015 (IICM-
2015) held in Indian Institute of Science Education and Research Thiruvananthapuram,
December 11-13, 2015.
• Poster Presentation: “Tuning the Solid State Optical Properties of Pyrene using C–HH–
C, C–HO and π–π Interactions” during ‘8th Asian Photochemistry Conference-
APC2014’ held at Taj Vivanta, Thiruvananthapuram, India, November 10-13, 2014.
• Poster Presentation: Progressive Acylation of Pyrene Engineers Solid State Packing and
Colour via. C–HH–C, C–HO and π–π Interactions” during 11th JNC Research
Conference on "Chemistry of Materials", Thiruvananthapuram, India, Oct 02-04, 2015.
• Poster Presentation: “DNA-Enforced Conformational Restriction of an Atropisomer” at
Organic Devices: the Future Ahead (ODeFA) held at Bhabha Atomic Research Centre,
Mumbai, India, March 3-6, 2014.
• Attended one day conference “ACS on Campus” an initiative from American Chemical
Society held at NIIST-Thiruvananthapuram, India, November 23, 2013.
• Attended Inter-IISER Chemistry Meet-2011 held at IISER-Thiruvananthapuram, India,
December, 2011.
Copyright and permission 192
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Photoinduced Excited State Processes in

Carbonylpyrenes: A Comparison between Solution

A thesis submitted for the degree of

Indian Institute of Science Education and Research

by me during my tenure as a Ph. D. student at the School of Chemistry, Indian Institute

of Science Education and Research Thiruvananthapuram. Such material as has been

Place: IISER Thiruvananthapuram Shinaj K. R.

Processes in Carbonylpyrenes: A Comparison between Solution and Solid-State

Properties” submitted by Shinaj K. R. was carried out by the candidate under my

Place: IISER Thiruvananthapuram Dr. Mahesh Hariharan

I thank to Dr. V. Sivaranjana Reddy for the TDDFT calculations. My wholehearted

I am indebted to Council of Scientific and Industrial Research (CSIR) and Department

1.3.1. Molecular dynamics revealed by transient spectroscopy 23

Figure Title Page

monomer in solution, high fluorescence quantum yields and the concentration

dependent shift of the emission spectrum upon excimer formation[6]. Monomeric

fluorescence markers to monitor dynamics of polymer chains and protein

structures[9-12]. After selective cysteine labelling of proteins with N-(l-

pyreny1)maleimide the appearance or absence of the excimer signal provides

compounds accessible for material applications.

1.2. Chemical modifications of pyrene

difference in chemical reactivity(Figure 1.2A). Therefore, the overview about reported

regions. Reactivity of pyrene at 1, 3, 6 and 8 positions toward electrophiles arise from

substituted pyrene derivatives[13]. Additionally, chemists have invented multistep

syntheses starting from benzene derivatives to achieve otherwise impossible

substitution of pyrene. 1-substituted and 1,3,6,8-tetrasubstituted pyrenes can be easily

accessible by direct electrophilic substitution of pyrene. The ease of preparation of

gives the possibility to straightforwardly introduce pyrene into different molecular

architectures. On the other hand, the selective preparation of pyrenes is challenging

three main groups of chemically identical sites.

highly required. It is crucial to obtain well-defined disubstituted pyrene building

1.3. Introduction to the photophysics of pyrene

Pyrene is an important polycyclic aromatic hydrocarbon[14, 15]. In 1954 Förster

and Kasper reported the first observation of intermolecular excimers in a pyrene

fluorescence quantum yield[17], exceptional distinction of the fluorescence bands for

monomer and excimer, and the sensitivity of its excitation spectra to

microenvironmental changes (Ham effect)[18] brought pyrene to the most explored

and well-studied organic molecule in terms of its photophysical properties.

Copyright © 2016 Elsevier).

occurs mediated by vibronic coupling of the electronic states (Figure 1.3B)[20].

to signals detected in ultrafast spectroscopy. From the S 1 state intersystem crossing

relax to the ground state.

1.3.1. Molecular dynamics revealed by transient spectroscopy

The S1 excited state lifetime of pyrene dissolved in methanol for a concentration

to negligible constant contributions on the ps time scale of the measurements. Foggi

within 150 fs measured by femtosecond transient spectroscopy in solution. They

1.4. Solid-state organization and optical properties

Light-emitting molecular solids and their potential utility in optical devices,

by the whole collective rather than by individual molecules. Studying molecular

conformational preferences required to correlate the structural facts with several

macroscopic properties, including their emission characteristics. Such systematic

knowledge pertaining to how complex properties emerge from collections of

solids, could be translated to deriving new strategies to control molecular

arrangement, to tune solid-state luminescent properties and also to obtain multi-

colour emission[23]. Noncovalent routes inclusive of polymorphism, phase transition,

nano/microcrystal forms and multi-component systems, have evolved as an efficient

method to draw such correlations with a minimum number of variables[24-26]. Also

it provides an opportunity to enhance the utility of a molecule of interest by

1.4.1. – interactions in polynuclear aromatic hydrocarbons