Oxidative Addition of Aryl Electrophiles to a Prototypical Nickel(0) Complex: Mechanism and Structure/Reactivity Relationships

Abstract

Detailed kinetic studies of the reaction of a model Ni 0 complex with a range of aryl electrophiles have been conducted. The reactions proceed via a fast ligand exchange preequilibrium, followed by oxidative addition to produce either [Ni I X(dppf)] (and biaryl) or [Ni II (Ar)X(dppf)]; the ortho substituent of the aryl halide determines selectivity between these possibilities. A reactivity scale is presented in which a range of substrates is quantitatively ranked in order of the rate at which they undergo oxidative addition. The rate of oxidative addition is loosely correlated to conversion in prototypical cross-coupling reactions. Substrates that lead to Ni I products in kinetic experiments produce more homocoupling products under catalytic conditions.