Guy Bertrand
| Guy Bertrand studied chemistry at the School of Chemistry of Montpellier and received his PhD from the University Paul Sabatier in Toulouse. After being a CNRS group leader (French National Center for Scientific Research) at the University of Toulouse, and then at the Laboratoire de Chimie de Coordination du CNRS, he has been the Director of the Laboratoire d'Hétérochimie Fondamentale et Appliquée at the University Paul Sabatier from 1998 to 2005. From 2001 to 2012 he served as the Director of the UCR/CNRS Joint Research Chemistry Laboratory, and since July 2012 he is Distinguished Professor and Director of the UCSD/CNRS Joint Research Chemistry Laboratory at the University of California San Diego. He is a member of the French Academy of Technology (2000), the Academia Europaea (2002), the European Academy of Sciences (2003), the French Academy of Sciences (2004), and is a Fellow of the American Association for the Advancement of Sciences (2006). He has recently received the Sir Ronald Nyholm Medal of the RSC (2009), the Grand Prix Le Bel of the French Chemical Society (2010), the Senior Humboldt Research Award, Re-invitation (2010), and the ACS Award in Inorganic Chemistry (2014). His most well known contribution is the discovery in 1988 of the first stable carbene, namely a (phosphino)(silyl)carbene A, three years prior to the report by Arduengo of a stable N-heterocyclic carbene. Bertrand is the originator of stable carbene chemistry. This was a truly striking discovery and was made long before anybody could imagine that stable carbenes would became ubiquitous ligands for transition-metal catalysts, or even organic catalysts in their own right. Since then, Guy Bertrand has made several ground breaking discoveries, which have furthered our understanding of the stability of carbenes, as exemplified by the isolation of cyclopropenylidene B, cyclo (alkyl)(amino)carbenes (CAACs) C, and mesoionic carbenes (MICs) D. Also of note is the preparation of the first stable carbo(dicarbene) or bent-allene E, nitrene F, and organoboron derivative G isoelectronic with amines. |