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85033164842
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Supporting Information
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Supporting Information.
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83
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85
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85033165635
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note
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-1) absorption at 890 nm.
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86
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4143138599
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Ph.D. Dissertation, Wayne State University
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Watzky, M.A.1
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93
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85033187140
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note
-
+.
-
-
-
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97
-
-
85033163144
-
-
note
-
The stabilization energy of the ground state and destabilization energy of the CT excited state do not enter into eq 2 because the perturbational horizontal displacement of the ground-state PE minimum results in the cancellation of these contributions (we are grateful to Dr. M. D. Newton for bringing this point to our attention).
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98
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For related arguments see: (a) Lever, A. B. P. Inorg. Chem. 1990, 29, 1271.
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(b) ibid. 1991, 30, 1980.
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101
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85033168533
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note
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79,80 For simplicity, only one component is considered here. There could also be a weak, high-energy MM'CT component as noted in Figure 5.
-
-
-
-
104
-
-
85033160437
-
-
note
-
-) upon metalation. The absorptivities of these bands are about 4 times larger in the ruthenates than in the parent dicyano complexes.
-
-
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105
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0001089818
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4143073555
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Endicott, J.F.1
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113
-
-
85033168241
-
-
note
-
For simplicity we label the electronic states by the center at which the charge is predominantly localized.
-
-
-
-
118
-
-
85033174164
-
-
note
-
1/2(obsd) and hDA. For theoretical definitions of the distance parameters see refs 2, 28, 29, and 49.
-
-
-
-
119
-
-
85033183610
-
-
note
-
DA = 5.2 Å.
-
-
-
-
120
-
-
85033162398
-
-
note
-
3+ complex. Owing to the uncertainty of this "correction", we have not included this point in Figure 10b.
-
-
-
-
122
-
-
85033179025
-
-
note
-
98 that the orthogonality relations would be rigorously applicable.
-
-
-
-
123
-
-
33751390961
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-
See footnote 41 of Lessard, R. B.; Heeg, M. J.; Buranda, T.; Perkovic, M. W.; Schwarz, C. L.; Rudong, Y.; Endicott, J. F. Inorg. Chem. 1992, 31, 3091.
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Rudong, Y.6
Endicott, J.F.7
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