Photoinduced Ligand-to-Metal Charge Transfer in Base-Metal Catalysis

被引:13
|
作者
Treacy, Sean M. [1 ]
Rovis, Tomislav [1 ]
机构
[1] Columbia Univ, Dept Chem, 3000 Broadway,Havemeyer Hall, New York, NY 10027 USA
来源
SYNTHESIS-STUTTGART | 2024年 / 56卷 / 02期
关键词
ligand-to-metal charge transfer; photocatalysis; base-metal catalysis; organic synthesis; photochemistry; photoredox catalysis; VISIBLE LIGHT-DRIVEN; PHOTOREDOX CATALYSIS; PHOTOCHEMICAL-REACTIONS; ORGANIC PHOTOREACTIONS; COBALT-CATALYSIS; TRANSITION-METAL; ETHYLENE-GLYCOL; OXIDATION; COMPLEXES; CHLORIDE;
D O I
10.1055/s-0042-1751518
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The absorption of light by photosensitizers has been shown to offer novel reactive pathways through electronic excited state intermediates, complementing ground-state mechanisms. Such strategies have been applied in both photocatalysis and photoredox catalysis, driven by generating reactive intermediates from their long-lived excited states. One developing area is photoinduced ligand-to-metal charge transfer (LMCT) catalysis, in which coordination of a ligand to a metal center and subsequent excitation with light results in the formation of a reactive radical and a reduced metal center. This mini review concerns the foundations and recent developments on ligand-to-metal charge transfer in transition-metal catalysis, focusing on the organic transformations made possible through this mechanism.
引用
收藏
页码:329 / 345
页数:17
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