Recent advances in FeCl3-photocatalyzed organic reactions via hydrogen-atom transfer

被引:33
|
作者
Yuan, Xiao-Ya [1 ]
Wang, Cong-Cong [1 ,2 ]
Yu, Bing [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
[2] Nanjing Forestry Univ, Natl Engn Res Ctr Low Carbon Proc & Utilizat Fores, Nanjing 210037, Peoples R China
关键词
FeCl; 3; Photocatalysis; Ligand-to-metal charge transfer; Hydrogen atom transfer; Chlorine radical; H BOND FUNCTIONALIZATION; ACTIVATION; GENERATION; PHOTOCATALYSIS; FRAGMENTATION; ALKYLATION; CATALYSIS; RADICALS; STRATEGY; MILD;
D O I
10.1016/j.cclet.2024.109517
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, FeCl 3 -photocatalyzed direct C-H/Si-H bond functionalization reactions have attracted huge attention. In those transformations, chlorine radical (Cl center dot ) could be generated from FeCl 3 via a ligandto-metal charge transfer (LMCT)/homolysis process under light irradiation. The resulting chlorine radical subsequently acts as a hydrogen atom transfer (HAT) agent to abstract the hydrogen atom of aliphatic C-H, O-H, or Si-H bonds to give the corresponding C/Si/O-centered radicals for various organic transformations. In this review, we summarized the recent advances in the application of FeCl 3 as a HAT photocatalyst for the C/Si-H functionalization to construct C-C, C-N, C-Si, C-S, C-B, and C -P bonds. (c) 2024 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页数:9
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