Chapter 20 Coordination Chemistry: Reactions of Complexes

Chapter 20 Coordination chemistry:
reactions of complexes
Ligand substituton reactions
Ligand substitution in square-planar complexes
Ligand substitution in octahedral complexes
Redox reactions
Photochemical reactions
Chapter 12 Coordination Chemistry IV:
Reaction and Mechanisms
12-1 History and Principles
12-2 Substitution Reactions
12-3 Kinetic Consequences of Reaction Pathways
12-4 Experimental Evidence in Octahedral substitution
12-5 Stereochemistry of Reactions
12-6 Substitution Reactions of Square-Planar Complexes
12-7 The trans Effect
12-8 Oxidation-Reduction Reactions
12-9 Reactions of Coordinated Ligand
“Inorganic Chemistry” Third Ed. Gary L. Miessler, Donald A. Tarr, 2004, Pearson Prentice Hall
http://en.wikipedia.org/wiki/Expedia
Chapter 12 Coordination Chemistry IV:
Reaction and Mechanisms
Share some characteristics with reactions of other
molecules.
Have some additional features because the

molecules have more complex (geometries,
rearrangement, metal atom etc.)
Substitution
Oxidation-Reduction
Reactions of Coordinated Ligand
History and Principles
The unification of reaction theory is still a goal of

chemists.
The ability to predict products and choose

appropriate reaction condition to obtain
the desired products is still a matter of art
as well as science.
Understand the electronic structure of the compounds

and their interactions.
the pass between the reactants and products is

always the lowest energy pathway and must be the
same regardless of the direction of the reaction – the
principle of microscopic reversibility.
Transition state vs Intermediate
A number of parameters can be obtained from kinetic

experiments.
Order, rate constant – the power of the reactant

concentration, the speed of reaction.
T – free energy, enthalpy and entropy of activation.

P – volume of activation
12-2 Substitution Reactions;
Inert and Labile compounds
Substitution or replacement
Compounds such
as these that react
rapidly are called
labile.
Inert or robust
Inert and Labile compounds
labile, inert vs stable, unstable
kinetic terms thermodynamic terms
Stable but labile
Unstable but inert Inert compounds are easy to study

Labile compound → How?
General rules Relationship with LFSA
Mechanisms of Substitution
; Dissociation (D)
The kinetic raw and other experimental evidence to

find out the mechanism of a reaction.
Dissociation
The steady-state hypothesis:

1. A very small concentration of a intermediate
2. The rates of the formation and reaction of the
intermediate must be equal.
; Dissociation (D)
Solving for [ML5]
The rate raw for the formation of the product

; Interchange (I)
Interchange
A rapid equilibrium between the incoming ligand and

the 6-coordinate reactant forms an ion pair or loosely
bonded molecular combination.
When k2 << k-1
The steady-state hypothesis

; Interchange (I)
If [Y] is large enough compared with [ML5X]→

Unstable transition species may be large
enough to significantly change the
concentration of the ML5X, but not that of Y.
and
; Interchange (I)
At low [Y] At high [Y]
Rate = k[M]0[Y]0 or Rate = (k/k’)[M]0

k[M]0[Y]0/[X] First order
Second order
; Association (A)
Association
The steady-state hypothesis
Second order
As with the dissociative mechanism, there are very
few clear examples of associative mechanism in
which the intermediate is detectable.
Most reaction fit better between the two extremes.
12-4 Experimental evidence in Octahedral substitution
; Dissociation
From six coordination (octahedral)

To five coordination (square pyramidal or trigonal-bipyramidal)
The change in LFSE between these two.
Ligand field activation energy (LFAE)

LFAE calculated for
trigonal-bipyramidal
transition states are
generally the same or
larger than those for
square-pyramidal.
Provide estimates of
the energy necessary
to form the transition
state.
; Dissociation
Thermodynamic favorable (∆H) vs reaction rate (EA)
Enthalpy, entropy, activation energy

; Dissociation
Stabilization energy for water exchange
The results are similar to those of the

thermodynamic case of enthalpy of
hydration
; Dissociation
Other metal ion facts that affect

reaction rates
1. Oxidation state of the central ion
Higher oxidation states have ???
ligand exchange rates
2. Ionic radius
Smaller ions have ??? ligand
exchange rates
Higher electronic attraction

; Dissociation
The evidence for dissociative

mechanism
1. The rate of reaction changes only slightly with changes in
the incoming ligand. (rate constant of less than a factor of
10)
2. Decreasing negative charge or increasing positive charge
on the reactant compound decreases the rate of
substitution.
3. Steric crowding on the reactant complex increases the rate
of ligand dissociation.
4. The rate of reaction correlates with the metal-ligand bond
strength of the leaving group, in a linear free energy
relationship (LFER).
5. Activation energies and entropies are consistent with
dissociation. (volume of activation ∆Vact; positive or
negative?)
; Linear Free Energy Relationship (LFER)
Many kinetic effects can be related to

thermodynamic effects by a LFER
The bond strength of a metal-ligand bond (a thermodynamic
function vs the dissociation rate of that ligand (a kinetic function).
the equilibrium constant (thermodynamic) vs the rate constant:
has to be linear relationship
Ea vs ∆H°
In molecular bonding term, a stronger bond between the metal
and the leaving group results in a larger activation energy.

Ea vs ∆H°

Ea vs ∆H°
For the first-order region

(large [Y]);
The rate constant are all
relatively close to that for
water exchange →
dissociative mechanism
For the second-order

region
; Associative Mechanism
Much less common
Ia Id
; Associative Mechanism
Much less common
Ia Id
Ia
Id
Why?
; The Conjugate Base Mechanism
The ligand trans to the amido or hydroxo group is frequently

the one lost
Additional evidence
1. Base catalyzed exchange of hydrogen from the amine groups
takes place under the same conditions.
2. The isotope ratio (18O/16O) in the product in 18O-enriched water is
the same as that in the water regardless of the leaving group. (no
associative)
3. RNH2 compounds react fast than NH3. (help to form 5-coordinate)
4. A plot of InkOH versus InKOH is linear.
5. When substituted amines used (no protons), the reaction is very
slow or nonexistent.
; The Conjugate Base Mechanism
The reaction in (a) is 104 times faster than that in (b)

; The Kinetic Chelate Effect
The increased energy

needed to remove the
first bound atom and
the probability of a
reversal of this first
step
The ligand must bend
and rotate to move the
free amine group away
from the metal.
The concentration of
the intermediate is low
and the first
dissociation can This kinetic chelate effect reduces the
readily reverse rates of aquation reactions by factors
from 20 to 105.
A common assumption is that reactions with dissociative

mechanisms are more likely to result in random
isomerization or racemization and associative
mechanisms are more likely to result in single-product
reactions; however, the evidence is much less clear-cut.
The higher concentration of ion pairs [Co(en)2Cl2]+·OH-

Temperature dependence
In the substitution of ammonia for both chlorides in
[Co(en)2Cl2]+
At low T: there is inversion of configuration
At high T: there is retention
Small fraction of trans
No complete explanation of these reactions
In some cases, a preferred orientation of the other ligands

may dictate the product.
the α form of trien complexes is more stable than the β form
; Substitution in trans complexes retention
Dissociation mechanism and

stereochemical change;
three different pathways
Square-pyramidal intermediate
Axial B requires more

arrangement of the ligands
and larger stretch for the
LL ring in the equatorial
plane tigonal-
bypyramidal
intermediate with
A change from trans to cis is B in the trigonal
plane
two thirds for a trigonal-
bipyramidal intermediate.
tigonal-
bypyramidal
intermediate with
B in the axial
position
; Substitution in trans complexes
; Substitution in trans complexes
Effect of the leaving ligand X.

; Substitution in cis complexes retention
three different pathways
Square-pyramidal intermediate
As a general rule, cis

reactants retain their cis
configuration, but trans
reactants are more likely to
give a mixture of cis and tigonal-
trans products. bypyramidal
intermediate with
B in the trigonal
plane
tigonal-
bypyramidal
intermediate with
B in the axial
position
; Isomerization of Chelate Rings
trigonal twist tetragonal twist; perpendicular
tetragonal twist; parallel Only possible; trigonal twist
Which one?
; Kinetics and stereochemistry of square-planar substitutions
; Evidence for associative reactions
Pt(II) is a soft acid, so soft ligand react

more readily
The order of ligands is nearly the reverse

The bond-strength effect of the metal-to-
ligand π bonding → ???
Each of the parameters s

and ηPt may change by a
factor of 3 from fast
reactions to slow reactions,
allowing for an overall ratio
of 106 in the rates.
12-7 The Trans Effect
It is possible to prepare specific

isomers different ligands
The order of trans effect

; explanations of the trans effect
Sigma-bond effects
Two factors
Weakening of the Pt-X bond
Stabilization of the presumed 5-coordinate transition state
σ-donor properties only

; explanations of the trans effect
Pi-bond effects
Stabilization of the presumed 5-coordinate transition state
Strong π–acceptor bond →

charge is removed from Pt →
the entrance of another ligand to form a 5-coordinate species
π-acceptor properties only
Overall trans effect

; inner- and outer-sphere reactions
Inner-sphere reaction; two molecules may be connected by a

common ligand
Outer-sphere reaction; two separate molecules
The rates show very large differences; depend on the ability of

the electrons to tunnel through the ligands
Ligands with π or p electrons or orbitals that can be used in
bonding provide good pathways for tunneling.
Change on electron transfer → change in bond distance

A higher ox. # leads to ___ bond
Form high spin Co(II)
To low spin Co(III)
eg orbitals are antibonding
Removal electrons from these orbitals → more stable compound
and shorter bond distances, large LFSE.
Inner-sphere reaction dissociation and bridging
Electron transfer
Association and separation

Inert
Labile Not allow formation of
But the parallels in the rate bridging species
constants of the two species
Inner-sphere mechanism
Inner-sphere mechanism;
Overall rate usually depends on the first two step
(substitution and transfer of electron)
bridging
The rate for Co compounds with other bridging ligands is
frequently as much as 105 larger than the rate for
corresponding Cr compounds
Seems to depend
more on the rate of
electron transfer
from Cr2+ to the
bridging ligand
electron transfer
from Cr2+ to metal
low-spin Ru(III)
; conditions for high and low oxidation number
The overall stability of complexes with different charges on the M
; LFSE, bonding energy, redox properties, the hard and soft
character
High oxidation # vs Low oxidation #
MnO4-, CrO42-, soft ligand

FeO42-, AgF2, cyanide
RuF5, PtF6, OsF6
V(CO)6, Cr(CO)6,
I- vs Cl-
Fe(CO)5
hard ligand ammonia
Strong oxidizing agent
Co(III) more stable

LFSE
high spin Co(II)
low spin Co(III)
12-9 Reactions of Coordinated Ligands
; hydrolysis of esters, amides, and peptides
The properties of ligand(organic compound) will be change by

coordinated to the metal.
; template reactions
The formation of the cyclic compound by coordination to a metal ion.

; template reactions
Imine or Schiff base
Geometric; formation of the complex brings the reactants into

close proximity with the proper orientation for reaction
Electronic; complexation may change the electronic structure
sufficiently to promote the reaction
; electrophilic substitution
Electrophilic Substitution on Acetylacetone

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Chapter 20 Coordination chemistry:

Ligand substituton reactions

Ligand substitution in square-planar complexes

Ligand substitution in octahedral complexes

12-1 History and Principles

12-2 Substitution Reactions

12-3 Kinetic Consequences of Reaction Pathways

12-4 Experimental Evidence in Octahedral substitution

12-5 Stereochemistry of Reactions

12-6 Substitution Reactions of Square-Planar Complexes

12-7 The trans Effect

12-8 Oxidation-Reduction Reactions

12-9 Reactions of Coordinated Ligand

Have some additional features because the

The unification of reaction theory is still a goal of

The ability to predict products and choose

Understand the electronic structure of the compounds

the pass between the reactants and products is

A number of parameters can be obtained from kinetic

Order, rate constant – the power of the reactant

T – free energy, enthalpy and entropy of activation.

kinetic terms thermodynamic terms

Stable but labile

Unstable but inert Inert compounds are easy to study

The kinetic raw and other experimental evidence to

The steady-state hypothesis:

Solving for [ML5]

The rate raw for the formation of the product

A rapid equilibrium between the incoming ligand and

The steady-state hypothesis

If [Y] is large enough compared with [ML5X]→

At low [Y] At high [Y]

Rate = k[M]0[Y]0 or Rate = (k/k’)[M]0

The steady-state hypothesis

From six coordination (octahedral)

Ligand field activation energy (LFAE)

Thermodynamic favorable (∆H) vs reaction rate (EA)

Enthalpy, entropy, activation energy

Stabilization energy for water exchange

The results are similar to those of the

Other metal ion facts that affect

Higher electronic attraction

The evidence for dissociative

Many kinetic effects can be related to

Many kinetic effects can be related to

Many kinetic effects can be related to

For the first-order region

For the second-order

Much less common

Much less common

The ligand trans to the amido or hydroxo group is frequently

The reaction in (a) is 104 times faster than that in (b)

The increased energy

A common assumption is that reactions with dissociative

The higher concentration of ion pairs [Co(en)2Cl2]+·OH-

In some cases, a preferred orientation of the other ligands

Dissociation mechanism and

Axial B requires more

Effect of the leaving ligand X.