A dual light-driven palladium catalyst: Breaking the barriers in carbonylation reactions

Author:

Torres Gerardo M.1ORCID,Liu Yi1ORCID,Arndtsen Bruce A.1ORCID

Affiliation:

1. Department of Chemistry, McGill University, 801 Sherbrooke St. W., Montreal, QC H3A 0B8, Canada.

Abstract

Lighting the way coming and going Catalysts accelerate chemical reactions by breaking existing bonds and then forming new ones. Often, the factors that favor the first process can muddle the second one, constraining a catalyst's generality. Torres et al. found that visible light excitation of a palladium complex can facilitate both the breaking and making of carbon-halogen bonds (see the Perspective by Kathe and Fleischer). The reaction specifically forms acid chlorides by carbonylation of a wide variety of alkyl or aryl bromides and iodides. These products in turn can react further to form amides and esters. Science , this issue p. 318 ; see also p. 242

Funder

McGill University

Natural Sciences and Engineering Research Council of Canada

Fonds de Recherche du Québec Nature et Technologies

Mexican National Council of Science and Technology

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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