化学
光化学
配体(生物化学)
催化作用
激发态
光催化
金属
光催化
钴
反应中间体
过渡金属
无机化学
有机化学
原子物理学
受体
物理
生物化学
作者
S M Treacy,Tomislav Rovis
出处
期刊:Synthesis
[Thieme Medical Publishers (Germany)]
日期:2023-11-21
卷期号:56 (13): 1967-1978
被引量:10
标识
DOI:10.1055/s-0042-1751518
摘要
Abstract 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. 1 Introduction 2 Iron 3 Cobalt 4 Nickel 5 Copper 6 Future Outlook and Conclusion
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