Hydrofunctionalization of olefins to value-added chemicals via photocatalytic coupling

被引:24
|
作者
Fan, Yonghui [1 ,2 ]
Li, Shenggang [1 ,3 ]
Bao, Jingxian [1 ,2 ]
Shi, Lei [1 ,2 ]
Yang, Yanzhang [1 ,4 ]
Yu, Fei [1 ,4 ]
Gao, Peng [1 ]
Wang, Hui [1 ]
Zhong, Liangshu [1 ,3 ]
Sun, Yuhan [1 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, Key Lab Low Carbon Convers Sci & Engn, Shanghai 201203, Peoples R China
[2] Shanghai Univ, Coll Sci, Dept Chem, Shanghai 200444, Peoples R China
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划;
关键词
MARKOVNIKOV; HYDROFORMYLATION; FUNCTIONALIZATION; MECHANISM; ALKENES; ALKYNES;
D O I
10.1039/c8gc00971f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A green strategy was developed for the synthesis of various value-added chemicals using methanol, acetonitrile, acetic acid, acetone and ethyl acetate as the hydrogen source by coupling them with olefins over heterogeneous photocatalysts. A radical coupling mechanism was proposed for the hydrofunctionalization of olefins with methanol to higher aliphatic alcohols over the Pt/TiO2 catalyst as the model reaction. C-H bond cleavage and C-C bond formation between photogenerated radicals and terminal olefins were accomplished in a single reaction at high efficiency. Our approach is atomically economical with high anti-Markovnikov regioselectivity and promising application potential under mild reaction conditions.
引用
收藏
页码:3450 / 3456
页数:7
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