| Literature DB >> 31306561 |
He Huang1, Zack M Strater2, Michael Rauch2, James Shee2, Thomas J Sisto2, Colin Nuckolls2, Tristan H Lambert1,2.
Abstract
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.Entities:
Keywords: C−H functionalization; Electrophotocatalysis; oxidation; radical dication; trisaminocyclopropenium ion
Year: 2019 PMID: 31306561 DOI: 10.1002/anie.201906381
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336