Photoredox Catalysis in Organophosphorus Chemistry

被引:128
作者
Luo, Kai [1 ,2 ,3 ]
Yang, Wen-Chao [1 ,2 ,3 ]
Wu, Lei [1 ,2 ,4 ,5 ]
机构
[1] Nanjing Agr Univ, Coll Sci, Jiangsu Key Lab Pesticide Sci, Nanjing 210095, Jiangsu, Peoples R China
[2] Nanjing Agr Univ, Coll Sci, Dept Chem, Nanjing 210095, Jiangsu, Peoples R China
[3] Nanjing Agr Univ, Coll Plant Protect, Nanjing 210095, Jiangsu, Peoples R China
[4] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[5] Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China
关键词
VISIBLE-LIGHT PHOTOREDOX; COUPLED ELECTRON-TRANSFER; C-H BONDS; METAL-FREE CONDITIONS; RADICAL-ADDITION; OXIDATIVE ADDITION; PHOSPHORANYL RADICALS; REDUCTIVE ELIMINATION; ARYLDIAZONIUM SALTS; HYDROGEN EVOLUTION;
D O I
10.1002/ajoc.201600512
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The vernal blooming of green chemistry has contributed to the development of visible light catalysis. Active radical species are generated from catalytic amounts of photosensitizers, such as transition-metal complexes and organic dyes, upon visible light irradiation. Stoichiometric amounts of oxidants, reductants, and radical initiators are avoided in most cases. Thus, reactions proceed under milder conditions with a broader functional group tolerance than found by other methods. Photoredox catalysis has been used to form C-C and C-X (X= O, N, and S) bonds but is comparably underdeveloped in organophosphorus chemistry. Herein, we summarize advances in photoredox catalysis that involve organophosphorus chemistry. The synthesis of organophosphorus compounds by photoredox catalysis, transition-metal complex/photoredox dual catalytic systems, and photoredox catalysis with phosphorus organocatalysts are discussed. The shortcomings and possible future trends of this chemistry are also presented.
引用
收藏
页码:350 / 367
页数:18
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