Mechanistic Investigation into the Gold-Catalyzed Decarboxylative Cross-Coupling of Iodoarenes
Ryan A. Daley, Aaron S. Morrenzin, Sharon R. Neufeldt, Joseph J. Topczewski
Abstract
While many gold-catalyzed reactions have been thoroughly developed, most are not thought to involve redox events at gold. In contrast, recent advances have demonstrated the feasibility of redox gold catalysis. This report describes a detailed mechanistic investigation of the gold-catalyzed decarboxylative cross-coupling, which likely proceeds via a high-valent Au(I/III) pathway. This investigation includes a kinetic analysis, stoichiometric experiments with Au(III) complexes, and density functional theory calculations. These data support a turnover-limiting oxidative addition to form a Au(III) aryl complex, with an off-cycle resting state. The dominant pathway appears to proceed through a silver-mediated decarboxylation with a subsequent Ag(I) to Au(III) transmetalation. These data provide some rationale for the significant counterion effects between SbF6– and NTf2–.