| Literature DB >> 30678456 |
Matthew Paeth1, Sam B Tyndall1, Liang-Yu Chen2, Jia-Cheng Hong2, William P Carson1, Xingwu Liu3,4, Xiaodong Sun3,4, Jinjia Liu3,4, Kundi Yang1, Elizabeth M Hale1, David L Tierney1, Bin Liu5, Zhi Cao3,4, Mu-Jeng Cheng2, William A Goddard6, Wei Liu1.
Abstract
Carbon-carbon bond-forming reductive elimination from elusive organocopper(III) complexes has been considered the key step in many copper-catalyzed and organocuprate reactions. However, organocopper(III) complexes with well-defined structures that can undergo reductive elimination are extremely rare, especially for the formation of Csp3-Csp3 bonds. We report herein a general method for the synthesis of a series of [alkyl-CuIII-(CF3)3]- complexes, the structures of which have been unequivocally characterized by NMR spectroscopy, mass spectrometry, and X-ray crystal diffraction. At elevated temperature, these complexes undergo reductive elimination following first-order kinetics, forming alkyl-CF3 products with good yields (up to 91%). Both kinetic studies and DFT calculations indicate that the reductive elimination to form Csp3-CF3 bonds proceeds through a concerted transition state, with a Δ H⧧ = 20 kcal/mol barrier.Entities:
Year: 2019 PMID: 30678456 DOI: 10.1021/jacs.8b12632
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419