Direct measurement of excited-state intervalence transfer in [(tpy)RuIII(tppz•-)RuII(tpy)]4+* by time-resolved near-infrared spectroscopy

被引：62
作者：
Dattelbaum, DM
Hartshorn, CM
Meyer, TJ
机构：
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
来源：
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2002年 / 124卷 / 18期
关键词：
D O I：
10.1021/ja010892i
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Extension of time-resolved infrared (TRIR) measurements into the near-infrared region has allowed the first direct measurement of a mixed-valence band in the metal-to-ligand charge transfer (MLCT) excited state of a symmetrical ligand-bridged complex. Visible laser flash excitation of [(tpy)Ru(tppz)Ru(tpy)]4+ (tppz is 2,3,5,6-tetrakis(2-pyridyl)pyrazine; tpy is 2,2′:6′,6″-terpyridine) produces the mixed-valence, MLCT excited state [(tpy)RuIII(tppż-)RuII(tpy)]4+* with the excited electron localized on the bridging tppz ligand. A mixed-valence band appears at ∇max = 6300 cm-1 with a bandwidth-at-half- maximum, Δ∇1/2 = 1070 cm-1. In the analogous ground-state complex, [(tpy)Ru(tppz)Ru(tpy)]5+, a mixed-valence band appears at max = 6550 cm-1 with Δ∇1/2 = 970 cm-1 which allows a comparison to be made of electronic coupling across tppz0 and tppż- as bridging ligands. Copyright © 2002 American Chemical Society.
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页码：4938 / 4939
页数：2
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