Upload
others
View
5
Download
0
Embed Size (px)
Citation preview
Understanding the Absorption Electronic Spectra ofCoordination Compounds using Crystal Field Theory
Chapter 20
Understanding the Absorption Electronic Spectra ofCoordination Compounds using Crystal Field Theory
Chapter 20
2
Review of the Previous Lecture
1. Used Molecular Orbital Theory and Group Theory to evaluate the covalency in metal ligand interactions
2. Explained the origins of the spectrochemical series by considering both and π metal ligand interactions donor ligands π donor ligands π acceptor ligands
3. Provided context for the 18 electron rule
4. Defined metal-ligand π back bonding with π acceptor ligands like CO Trans influence
3
1. Electronic spectroscopy pertaining to d-orbital e- (Introduction)
Typically occur in the visible range of light.
A. The Spectrochemical Series
4
I- < Br - < [NCS]- < Cl- < F- < [OH]- < [ox]2- ~ H2O < [NCS]- < NH3 < en < [CN]- ~ CO
Weak field ligands Strong field ligandsLigands increasing Δoct
Small Δ High spin π donors
Large Δ Low spin π acceptors
σ donor
Cobalt (III) Octahedral Complexes; d6
5
Weak field vs Strong field extremities dictated by ligand coordination.
Small ΔoctWeak Field, High spin
S = 2
Big ΔoctStrong Field, Low spin
S = 0
Δoct
ΔoctE
t2g
eg
t2g
eg
d-d electronic transition and Δoct
6
Δoct = E = hν = h c λ̶
Δoct , λ
7
3+
I- < Br - < [NCS]- < Cl- < F- < [OH]- < [ox]2- ~ H2O < [NCS]- < NH3 < en < [CN]- ~ CO
L = CN- L = NH3 L = H2O
Cobalt (III) Octahedral Complexes; d6
8
B. Electronic transition selection rules
1. Spin rule: Transitions must not involve a change of spin.
ΔS = 0
2. Laporte rule: Transitions must have a change of parity.
Gerade Ungerade
No gerade gerade nor ungerade ungerade
Technically all d-d electronic transitions are Laporte forbidden
gerade gerade
9
I. Spin forbidden d-d e- transitions
[Mn(H2O)6]2+ is high-spin d5 Mn(II):
S = 2.5 S = 1.5
t2g
eg
Extremely weak transitions; ε < 1 M-1cm-1
RECALL Beer’s Law: A = ε b c
ε is a property of the absorbance of a chemical species A measure of the intensity of an electronic transition
10
II. Spin-allowed d-d e- transitions
A. For ideal octahedral complexes, d-d e- transitions that are spin-allowed but Laporte forbidden
Extremely weak transitions; ε = 10 - 200 M-1cm-1
i.e. [Co(H2O)6]3+ is high-spin d6 Co(III):
S = 2 S = 2
t2g
eg
11
II. Spin-allowed d-d e- transitions
B. For ideal tetrahedral complexes, d-d e- transitions are spin-allowed but “less” Laporte forbidden than octahedral complexes because they are non-centrosymmetric complexes.
ε = 100 – 1,000 M-1cm-1
i.e. [NiCl4]2- is high-spin d8 Ni(II):
S = 1 S = 1e
t2 t2
e
12
2. Charge transfer electronic transitionsCharge transfer e- transitions are Spin and Laporte allowed; ε > 1,000 M-1cm-1
Typically observed in the UV range of light whereas d-d electronic transitions are typically observed in the Visible range of light.
A. Ligand to metal charge transfer (LMCT)
Transfer of an electron from an orbital with primarily ligand character to one with primarily metal character
Can be observed with π donor ligands
M Le-
Revisit Molecular Orbital Diagram including π interaction with Weak Field Ligands
13
[CoF6]3-
Co3+ ; d6
High spin, S = 2
Revisit Molecular Orbital Diagram including π interaction with Weak Field Ligands
14
[CoF6]3-
Co3+ ; d6
High spin, S = 2
LMCT Bands
15
2. Charge transfer electronic transitions
B. Metal to ligand charge transfer (MLCT)
Transfer of an electron from an orbital with primarily metal character to one with primarily ligand character
Can be observed with π acceptor ligands
M Le-
16
Revisit Molecular Orbital Diagram including π interaction with Strong Field Ligands [Co(CO)6]3+
Co3+ ; d6
Low spin, S = 0
MLCT Bands
LMCT Bands
17
3. Solution preparations to observe e- transitions
1. Concentrated solutions of coordination complexes need to be made to observe d-d e- transitions• Lower energy transitions• ε < 1,000 M-1cm-1
• mM concentrations
2. Dilute solutions of coordination complexes need to be made to observe charge transfere- transitions• Higher energy transitions• ε > 1,000 M-1cm-1
• μM concentrations