Proton-Coupled Electron Transfer Originating from Excited States of Luminescent Transition-Metal Complexes

被引:75
作者
Wenger, Oliver S. [1 ]
机构
[1] Univ Gottingen, Inst Anorgan Chem, D-3400 Gottingen, Germany
关键词
electron transfer; proton transfer; reaction dynamics; time-resolved spectroscopy; transition metals; ACID-BASE PROPERTIES; HYDROGEN-ATOM TRANSFER; RUTHENIUM(II) COMPLEXES; PHOTOSYSTEM-II; OSMIUM COMPLEXES; PHOTOPHYSICAL PROPERTIES; TRANSFER PATHWAYS; REDOX PROPERTIES; SALT BRIDGES; FREE-ENERGY;
D O I
10.1002/chem.201102011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Proton-coupled electron transfer (PCET) is of fundamental importance for small-molecule activation processes, such as water splitting, CO2-reduction, or nitrogen fixation. Ideally, energy-rich molecules such as H-2, CH3OH, or NH3 could be generated artificially using (solar) light as an energy input. In this context, PCETs originating directly from electronically excited states play a crucial role. A variety of transition-metal complexes have been used recently for fundamental investigations of this important class of reactions, and the key findings of these studies are reviewed in this article. The present minireview differs from other reviews on the subject of PCET in that it focuses specifically on reactions occurring directly from electronically excited states.
引用
收藏
页码:11692 / 11702
页数:11
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