Catalytic C–F bond activation of geminal difluorocyclopropanes by nickel(i) complexes via a radical mechanism†
Jan Wenz,Christoph A. Rettenmeier,Hubert Wadepohl,Lutz H. Gade
Chemical Communications Pub Date : 11/13/2015 00:00:00 , DOI:10.1039/C5CC08950F
Abstract

Nickel(II) fluorido complexes bearing NNN-pincer ligands were found to be catalysts in the hydrodefluorination of geminal difluorocyclopropanes which undergo ring-opening to form the corresponding monofluoroalkenes in good yield and high Z-selectivities. Evidence for a radical based mechanism involving nickel(I) and nickel hydrido complexes as key intermediates was obtained in the corresponding stoichiometric reactions.

Graphical abstract: Catalytic C–F bond activation of geminal difluorocyclopropanes by nickel(i) complexes via a radical mechanism