Photoinduced ligand-to-metal charge transfer (LMCT) in organic synthesis: reaction modes and research advances

被引:1
|
作者
Yang, Yingying [1 ]
Huang, Xinxiang [1 ]
Jin, Yi [1 ]
机构
[1] Yunnan Univ, Yunnan Prov Ctr Res & Dev Nat Prod, Sch Pharm, Key Lab Med Chem Nat Resource,Minist Educ, Kunming 650091, Peoples R China
基金
中国国家自然科学基金;
关键词
C BOND-CLEAVAGE; COUPLING REACTIONS; GENERATION;
D O I
10.1039/d4cc06099g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, visible light-induced ligand-to-metal charge transfer (LMCT) has emerged as an attractive approach for synthesizing a range of functionalized molecules. Compared to conventional photoredox reactions, photoinduced LMCT activation does not depend on redox potential and offers diverse reaction pathways, making it particularly suitable for the activation of inert bonds and the functional modification of complex organic molecules. This review highlights the indispensable role of photoinduced LMCT in synthetic chemistry, with a focus on recent advancements in LMCT-mediated hydrogen atom transfer (HAT), C-C bond cleavage, decarboxylative transformations, and radical ligand transfer (RLT) reactions.
引用
收藏
页码:1944 / 1961
页数:18
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