Halide-Dependent Mechanisms of Reductive Elimination from Gold(III)

Abstract

Two unique organometallic halide series (Ph3P)Au(4-Me-C6H4)(CF3)(X) and (Cy3P)Au(4-F-C6H4)(CF3)(X) (X = I, Br, Cl, F) have been synthesized. The PPh3-supported complexes can undergo both Caryl–X and Caryl–CF3 reductive elimination. Mechanistic studies of thermolysis at 122 °C reveal a dramatic reactivity and kinetic selectivity dependence on halide ligand. For X = I or F, zero-order kinetic behavior is observed, while for X = Cl or Br, kinetic studies implicate product catalysis. The selectivity for Caryl–CF3 bond formation increases in the order X = I < Br < Cl < F, with exclusively Caryl–I bond formation when X = I, and exclusively Caryl–CF3 bond formation when X = F. Thermodynamic measurements show that Au(III)–X bond dissociation energies increase in the order X = I < Br < Cl, and that ground state Au(III)–X bond strength ultimately dictates selectivities for Caryl–X and Caryl–CF3 reductive elimination.