| Literature DB >> 29710939 |
Mark T Miller1, Peter K Gantzel1, Timothy B Karpishin1.
Abstract
Unprecedented stabilization of the copper(I) oxidation state is demonstrated for the complex cation [Cu(bfp)2 ]+ (1) due to the steric and electronic effects of the CF3 groups (E1/2 (CuII /CuI )=+1.55 V vs. SCE). The redox existence range of the copper(I) species is remarkably high at 2.77 V. It is emissive in solution at room temperature and shows great potential as a photocatalyst; in the excited state it is a very potent photooxidant. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.Entities:
Keywords: Copper; Cyclic voltammetry; Electrochemistry; N ligands; Photochemistry
Year: 1998 PMID: 29710939 DOI: 10.1002/(SICI)1521-3773(19980619)37:11<1556::AID-ANIE1556>3.0.CO;2-W
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336