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85087249093
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note
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+) seem to reflect the predominant increase in the energy of the π* level (due to back-bonding interactions) compared to the changes in the ground-state π level.
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2542435335
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note
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n- complexes.
-
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66
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0020765087
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4243560805
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red values are related by a solvational energy term, which remains constant for the whole series and may be included in χ (cf. also ref 40).
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Dodsworth, E.1
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2542487697
-
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note
-
MLCT values for the ruthenium and osmium complexes, because of spin-orbit coupling effects. This was not the case for iron, as no band asymmetry was found, and thus the measured maximum energy corresponds to the unsplit case, i.e. the weighted average of the A and E states (see Figure 3). For osmium, however, the high-energy component (transition to the E state) must be diminished by 1/2λ in order to obtain an energy value free of spin-orbit effects. The same subtraction was performed for the ruthenium complex.
-
-
-
-
72
-
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85087248026
-
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note
-
n- series are scarce in the literature (cf. ref 10). Our measurements for several L ligands show a trend similar to those found for iron and osmium complexes.
-
-
-
-
74
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85087247885
-
-
note
-
act = 25 kcal/mol.
-
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-
-
75
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0003505641
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Springer-Verlag: Berlin, Heidelberg, Germany, New York
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Williams, A. F. A Theoretical Approach to Inorganic Chemistry; Springer-Verlag: Berlin, Heidelberg, Germany, New York, 1979; p 255.
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Williams, A.F.1
-
76
-
-
85087249910
-
-
note
-
III" character made available by the π-acid ability of cyanides. This is consistent with the relative solvatochromic changes of the MLCT bands, showing that Os is the strongest π-donor.
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