指示
氧化剂
化学
光激发
催化作用
光催化
自由基离子
苯
光化学
离子
电子转移
可见光谱
激发态
有机化学
材料科学
物理
核物理学
光电子学
作者
He Huang,Zack M. Strater,Michael Rauch,James Shee,Thomas J. Sisto,Colin Nuckolls,Tristan H. Lambert
标识
DOI:10.1002/anie.201906381
摘要
Visible-light photocatalysis and electrocatalysis are two powerful strategies for the promotion of chemical reactions. Here, these two modalities are combined in an electrophotocatalytic oxidation platform. This chemistry employs a trisaminocyclopropenium (TAC) ion catalyst, which is electrochemically oxidized to form a cyclopropenium radical dication intermediate. The radical dication undergoes photoexcitation with visible light to produce an excited-state species with oxidizing power (3.33 V vs. SCE) sufficient to oxidize benzene and halogenated benzenes via single-electron transfer (SET), resulting in C-H/N-H coupling with azoles. A rationale for the strongly oxidizing behavior of the photoexcited species is provided, while the stability of the catalyst is rationalized by a particular conformation of the cis-2,6-dimethylpiperidine moieties.
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