chapter 7 transition metal complexes -...
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Chapter 7 Transition Metal Complexes
Our focus will be on the physical consequences that follow from the symmetry of transition metal complexes not the standard coordination chemistry or inorganic chemistry.
7.5 Splitting of Terms
7.4 Terms of Free Ions with dn Configurations
7.6 Electronic Structure of Transition Metal Complexes
7.3 Molecular Orbital Approach to Bonding in Complexes
7.2 Jahn-Teller Distortions and other Crystal Fields
7.1 Crystal Field Theory
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7.1 Crystal Field Theory
Verify the fact that the d orbitals in an Oh field must divide into two degenerate sets.
The effect of a symmetry operation on an orbital is only a change in coordinates without a change in energy. Thus, if some operation converts two or more orbitals into each other, they must be energetically equal (degenerate).
Three p orbitals must be degenerate
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7.1 Crystal Field Theory
in the case of five d orbitals
Interchange among themselves and must be degenerate
Not transformed directly into each other, they are transformed into functions that are linear combinations of each other.Must have the same energy
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7.1 Crystal Field Theory
Now, we know that the d orbitals in an octahedral complex divide into a triply degenerate set and a doubly degenerate set.
We do not know yet about the symmetries. For this take the five wave functions as a basis.
We can obtain the following reducible representation.
Γd = Eg + T2g
T2g
Eg
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7.1 Crystal Field Theory
Give the characters for operations in spherical symmetry (the group R3).These relationships can be used with Oh or any other point group, because all point groups are subgroups of R3.
The quantum number j can be replaced by l when considering an orbital, L when considering Russell-Saunders term.For the sign, orbitals with even-value (s, d, g,…) are gerade (+) and orbitals with odd-value (p, f,…) are ungerade (-).
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7.1 Crystal Field Theory
The relative energy order to determine.
If a transition metal ion were placed in a spherical fieldequivalent to the charges on six ligands, the energies of all five d orbitals would rise together.
However in octahedralarrangement.
More repulsions because the lobes of the orbitals in the eg set point directly at the ligands
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7.1 Crystal Field Theory
This results in no net energy change for the system.
The magnitude of Δo depends upon both the metal ion and the attaching ligands.
More repulsion
Less repulsion
Splitting of d orbitals in an Oh field
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Crystal field stabilization energy (CFSE);the actual distribution vs the uniform field.Good for the concept of the repulsion of orbitals by the ligands but no explanation for bonding in coordination complexes.
7.1 Crystal Field Theory
Free ion OhR3
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7.1 Crystal Field Theory
The relative magnitudes of Δoand the mean pairing energy, P, determine which spin state results.
Electron configuration
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7.1 Crystal Field Theory
CFT considerations to tetrahedrally structured complexes
More repulsions in the t2 set
Γd = E + T2
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7.2 Jahn-Teller Distortion and Other Crystal Fields
Group-subgroup
Splitting as a result of stretching
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7.2 Jahn-Teller Distortion and Other Crystal Fields
Splitting as a result of removing two axial ligands
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7.3 Molecular Orbital Approach to Bonding in Complexes
Unlike CFT and LFT models, we will include consideration of interactions with metal ion s and p orbitals.
We take six vectors pointing toward the center of a Cartesian coordination system as our basis for a reducible representation of SALCs Γσ.
Γσ = A1g + Eg + T1u, six SALCs with three different symmetries.
To identify the symmetries of metal ion AOs, investigate the character table.
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7.3 Molecular Orbital Approach to Bonding in Complexes
SALC with A1g symmetry and s orbital of the central metal
SALCs with Eg symmetry and dz2 and dx2-y2 orbitals of the central metal
SALCs with T1u symmetry and three p orbitals of the central metal
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7.3 Molecular Orbital Approach to Bonding in Complexes
MO diagram with only sigma bonding
CFT
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7.3 Molecular Orbital Approach to Bonding in Complexes
Delocalization of eg* electron density and Δo
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7.3 Molecular Orbital Approach to Bonding in Complexes
To include pi-bonding in our MO
Γπ = T1g + T2g + T1u + T2u, twelve SALCs with four different symmetries.
Identify the symmetries of metal ion AOs, investigate the character table.
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7.3 Molecular Orbital Approach to Bonding in Complexes
SALCs with T2g
SALCs with T1u
Will interact three d orbitals (dxy, dyz, dxz)
Will interact three p orbitals (px, py, pz)
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7.3 Molecular Orbital Approach to Bonding in Complexes
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7.3 Molecular Orbital Approach to Bonding in Complexes
For tetrahedrally structured complexes, sigma bonding
Γσ = A1 + T2,
Γπ = E + T1 + T2.
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7.3 Molecular Orbital Approach to Bonding in Complexes
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7.4 Terms of Free Ions with dn Configuration
In the case of a single electron in a degenerate set of five d orbitals, the electron can have any of the values ml = +2, +1, 0, -1, -2 and either of the values ms = +1/2, -1/2.Thus, there are 10 ways of arranging the electron, making a total of 10 microstates.
Both the individual orbital magnetic moments and spin magnetic moments will interact with one another, resulting in an energy state or term for the configuration.
The Russell-Saunders coupling scheme usually gives an adequate approximation of observed behavior.
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Carbon atomEnergy levels for the p2 electrons→ Five energy levelsEach energy levels can be described as a combination of the mland ms values of the 2p electrons.
The orbital angular momenta and the spin angular momenta of the 2p electrons interact in a manner called Russell-Saunders coupling (LS coupling).
2p electrons
n = 2, l = 1ml = +1, 0, or -1ms = +1/2 or -1/2
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How many possible combinations of ml and ms values?
One possible set of values for the two electrons in the p2
configuration would be
First electron: ml = +1 and ms = +1/2Second electron: ml = 0 and ms = -1/2
microstates
Russell-Saunders coupling (LS coupling)
Orbit-orbit couplingML = ∑ml→ L: total orbital angular momentum quantum number
Spin-spin couplingMs = ∑ms→ S: total spin angular momentum quantum number
Spin-orbit couplingJ = L + S : total angular momentum quantum number
2p electrons
n = 2, l = 1ml = +1, 0, or -1ms = +1/2 or -1/2Notation 1+0-
microstate
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Electronic quantum # (ml and ms) to atomic quantum #(ML and MS)
microstates
2p electrons
n = 2, l = 1ml = +1, 0, or -1ms = +1/2 or -1/2
Tabulate the possible microstates1. No two electrons in the same microstate have identical quantum
numbers (the Pauli exclusion principle)2. Count only the unique microstates (1+0- and 0-1+)
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L and S describe collections of microstates.ML and MS describe the microstates themselves.
Atomic States Individual ElectronsML = 0, ±1, ± 2,… ± L ml = , ±1, ± 2,… ± l MS = S, S-1,…. –S ms = +1/2, -1/2
Term symbol
Term Symbol
2S+1LJ
L = 0, 1, 2, 3 → S, P, D, F
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Electronic quantum # (ml and ms) to atomic quantum #(ML and MS) → describe states of multielectron atoms
Free-ion terms are very important in the interpretation of the spectra of coordination compounds.
1S (singlet S) : S → L = 0 → ML = 0, 2S+1 =1 → S =0 → MS = 0
0+0-0
0
ML
MS
The minimum configuration of two electrons
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2P (doublet P) : P → L = 1 → ML = +1,0,-12S+1 =2 → S =1/2 → MS = +1/2, -1/2
ML
MS
The minimum configuration of one electron
-1+-1--1
0+0-0
1+1-+1
+1/2-1/2
Six microstates
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ML
MS
-1+-1--1
0+0-0
1+1-+1
+1/2-1/2
Six microstates
xx-1
xx0
xx+1
+1/2-1/2
The spin multiplicity is the same as the # of microstates
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7.4 Terms of Free Ions with dn Configuration
Term symbol 2S+1L
L may be 0, 1, 2,…S may be 0, ½, 1, 2/3…2S+1; multiplicity
The L values that result from the possible ways in which l values can be combined for the configurations p2 and d2.
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7.4 Terms of Free Ions with dn Configuration
ML = L, L-1….-L
MS = S, S-1,.. -S
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7.4 Terms of Free Ions with dn Configuration
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Reduce microstate table into its component free-ion terms.
The spin multiplicity is the same as the # of microstates.
Each terms has different energies; they represent three states with different degrees of electron-electron interactions.
Which term has the lowest energy. This can be done by using two of Hund’s rules.
1. The ground term (term of lowest energy) has the highest spin multiplicity. (Hund’s rule of maximum multiplicity)
2. If two or more terms share the maximum spin multiplicity, the ground term is one having the highest value of L.
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Reduce microstate table into its component free-ion terms.
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d2
l = 2ml = +2, +1 0, -1, -2ms = +1/2 or -1/2
x-4
xxxxx-3
xxxxx-2
xxxxxxxx-1
xxxxxxxxx0
xxxxxxxx+1
xxxxx+2
xxxxx+3
x+4
-10+1
ML
MS
1S1D1G3P3F
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7.5 Splitting of Terms
The possible splitting of S, P, D, F
And S state is nondegenerate; no splittingP term from Eqs. 7.2 ~ 7.6
T1g; in Oh a P term is not split, but becomes a triply degenerate T1gterm
D term has a fivefold orbital degeneratefrom Eqs. 7.2 ~ 7.6
ΓD = Eg + T2g
F term has a sevenfold orbital degeneratefrom Eqs. 7.2 ~ 7.6
ΓF = A2g + T1g + T2g
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7.5 Splitting of Terms
for d2
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7.5 Splitting of Terms
We need to know the term symbols arising from 45 microstates in the slightly relaxed strong-field case.
Setup fot preparation a correlation diagram for a d2
ion in Oh environment
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Electronic Spectra of Coordination Compounds
Identify the lowest-energy term
1. Sketch the energy levels, showing the d electrons.
2. Spin multiplicity of lowest-energy state = number of unpaired electrons + 1.
3. Determine the maximum possible value of ML for the configuration as shown. This determines the type of free-ion term.
4. Combine results of steps 2 and 3 to get ground term.
Spin multiplicity = 3+1=4
Max. of ML: 2+1+0 =3
4F
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7.5 Splitting of Terms
For the ground-state configuration t2g2 we take the direct product t2g X t2g
Γ(t2g2) = A1g + Eg + T1g + T2g
We need to know spin multiplicities. Here Dt = 15.Three possible ways
The triplet state must have a triply degenerate orbitals term
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7.5 Splitting of Terms
For the ground-state configuration eg2 we take the direct product eg X eg
Γ(eg2) = A1g + A2g + Eg
We need to know spin multiplicities. Here Dt = 6.Two possible ways
The triplet state must have nondegenerate orbitals term
Γ(eg2) = 3A1g + 1A2g + 1Eg
Γ(eg2) = 1A1g + 3A2g + 1Eg
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7.5 Splitting of Terms
For the ground-state configuration t2g1eg
1 we take the direct product t2g X eg
Γ = T1g + T2g
We need to know spin multiplicities. Here Dt = 24.The electrons in this configuration are unrestricted by the Pauliexclusion principle. And they can occur as both singlets and triplets
Γ = 1T1g + 1T2g + 3T1g + 3T2g
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7.5 Splitting of Terms
Γ = 1T1g + 1T2g + 3T1g + 3T2g
Γ(eg2) = 3A1g + 1A2g + 1Eg
Γ(eg2) = 1A1g + 3A2g + 1Eg
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7.5 Splitting of Terms
Γ = 1T1g + 1T2g + 3T1g + 3T2g
Γ(eg2) = 3A1g + 1A2g + 1Eg
Γ(eg2) = 1A1g + 3A2g + 1Eg
Correlation diagram for a d2
ion in Oh environment
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7.5 Splitting of Terms
Correlation diagram for a d8
ion in Oh environment
eg2
t2g2
t2g1eg
1
in d2 system
![Page 46: Chapter 7 Transition Metal Complexes - Yonseichem.yonsei.ac.kr/chem/upload/CHE6201-01/124185240269303.pdf · 7.6 Electronic Structure of Transition Metal Complexes 7.3 Molecular Orbital](https://reader031.vdocuments.us/reader031/viewer/2022012314/5acbac267f8b9a27628b97c4/html5/thumbnails/46.jpg)
7.6 Electronic Spectra of Transition Metal Complexes
The most striking feature of transition metal complexes is the array of colors they present.
Color results when a complex absorbs frequencies in the visible region of the spectrum, causing transitions from the ground electronic states to certain of the excited states of the configurations.
Since the electronic states arise from d-electron configurations on the metal ion, the absorptions are said to result d-d transitions.
1. Transitions between states of the same parity are forbidden (symmetry with respect to a center of inversion.: Laporte selection rule
2. Transitions between states of different spin multiplicities are forbidden: spin selection rule
4A2 and 4T1: spin-allowed4A2 and 2T2: spin-forbidden
Forbidden;g → g transitionallowed; g → u transition
![Page 47: Chapter 7 Transition Metal Complexes - Yonseichem.yonsei.ac.kr/chem/upload/CHE6201-01/124185240269303.pdf · 7.6 Electronic Structure of Transition Metal Complexes 7.3 Molecular Orbital](https://reader031.vdocuments.us/reader031/viewer/2022012314/5acbac267f8b9a27628b97c4/html5/thumbnails/47.jpg)
Some rules for relaxation of selection rules
1. Vibrations may temporarily change the symmetry(the center of symmetry is temporarily lost: vibronic couplingrelax the first selection rule:d-d transition
2. Tetrahedral complexes often absorb more strongly than Ohcomplexes. Metal-ligand sigma bonds can be described as involving a combination of sp3 and sd3 hybridization of the metal orbitals: relax the first selection rule
3. spin-orbit coupling provides a mechanism of relaxing the second selection rule
7.6 Electronic Spectra of Transition Metal Complexes
![Page 48: Chapter 7 Transition Metal Complexes - Yonseichem.yonsei.ac.kr/chem/upload/CHE6201-01/124185240269303.pdf · 7.6 Electronic Structure of Transition Metal Complexes 7.3 Molecular Orbital](https://reader031.vdocuments.us/reader031/viewer/2022012314/5acbac267f8b9a27628b97c4/html5/thumbnails/48.jpg)
Correlation diagram for a d8
ion in Oh environment
7.6 Electronic Spectra of Transition Metal Complexes