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The Yb@g-C3N4 Dual-Functional Photocatalytic Fluoroalkylation of 2-Isocyanides with RfSO2Cl as Both a Fluoroalkyl Radical Source and HAT Reagent

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成果类型:
期刊论文
作者:
Peng, Qiong-Hui;Jiang, Jun;Liao, Zhi-Hao;Wu, Zhi-Lin;Ou, Li-Juan;...
通讯作者:
He, WM;Ou, LJ
作者机构:
[Liao, Zhi-Hao; Wu, Zhi-Lin; Peng, Jia; He, Wei-Min; Dai, Hui; Peng, Qiong-Hui; Jiang, Jun; He, WM] Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
[Jiang, Jun] Nanjing Forestry Univ, Coll Chem Engn, Nanjing 210037, Peoples R China.
[Ou, Li-Juan] Hunan Inst Technol, Sch Mat Sci & Engn, Hengyang 421002, Peoples R China.
通讯机构:
[Ou, LJ ] H
[He, WM ] U
Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
Hunan Inst Technol, Sch Mat Sci & Engn, Hengyang 421002, Peoples R China.
语种:
英文
关键词:
N -heteroarenes;fluoroalkylation;isocyanide;chloride radical;hydrogen atom transfer
期刊:
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
ISSN:
2168-0485
年:
2025
卷:
13
期:
28
页码:
10971–10977
基金类别:
University of South China; University of South China
机构署名:
本校为第一且通讯机构
院系归属:
化学化工学院
摘要:
The first example of the dual-functional photocatalytic fluoroalkylation of 2-isocyanides with R f SO 2 Cl catalyzed by Yb@g-C 3 N 4 has been accomplished by simultaneously coupling the photogenerated electron-driven reductive production of fluoroalkyl radicals with the photogenerated hole-driven oxidative production of chloride radicals. This strategy not only fully utilizes photogenerated electron–hole pairs for bond formation but also avoids the use of exogenous chloride salts, additional redox reagents, and sacrificial electron donors/acce...

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