Isotope Effects Reveal the Catalytic Mechanism of the Archetypical Suzuki-Miyaura Reaction.

Experimental and theoretical C kinetic isotope effects (KIEs) are utilized to obtain atomistic insight into the catalytic mechanism of the Pd(PPh)-catalyzed Suzuki-Miyaura reaction of aryl halides and aryl boronic acids. Under catalytic conditions, we establish that oxidative addition of aryl bromides occurs to a 12-electron monoligated palladium complex (Pd-(PPh)). This is based on the congruence of the experimental KIE for the carbon attached to bromine (KIE = 1.020) and predicted KIE for the transition state for oxidative addition to the Pd(PPh) complex (1.021). For aryl iodides, the near-unity KIE of ~1.003 suggests that the first irreversible step in the catalytic cycle precedes oxidative addition and is likely the binding of the iodoarene to Pd(PPh). Our results suggest that the commonly proposed oxidative addition to the 14-electron Pd(PPh) complex can occur only in the presence of excess added ligand or under stoichiometric conditions; in both cases, experimental KIE of 1.031 is measured, which is identical to the predicted KIE for the transition state for oxidative addition to the Pd(PPh) complex (1.031). The transmetalation step, under catalytic conditions, is shown to proceed via a tetracoordinate boronate (8B4) intermediate with a Pd-O-B linkage based on the agreement between an experimental KIE for the carbon atom involved in transmetalation (KIE = 1.035) and a predicted KIE for the 8B4 transmetalation transition state (1.034).