Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, 14853, USA.
Department of Chemistry, Columbia University, New York, NY, 10027, USA.
Angew Chem Int Ed Engl. 2019 Sep 16;58(38):13318-13322. doi: 10.1002/anie.201906381. Epub 2019 Aug 2.
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.
可见光照相催化和电催化是促进化学反应的两种强大策略。在这里,这两种方式结合在一个光电催化氧化平台中。这种化学方法采用三氨基环丙烯鎓(TAC)离子催化剂,它被电化学氧化形成环丙烯鎓自由基二阳离子中间物。自由基二阳离子通过可见光激发产生具有氧化能力(3.33 V 相对于 SCE)的激发态物种,足以通过单电子转移(SET)氧化苯和卤代苯,通过 C-H/N-H 偶联与唑类化合物反应。提供了对光激发物种强氧化行为的原理,同时通过 cis-2,6-二甲基哌啶部分的特定构象来合理化催化剂的稳定性。