Chromium-Salen Catalyzed Cross-Coupling of Phenols: Mechanism and Origin of the Selectivity

A highly chemoselective phenol cross-coupling reaction catalyzed by a Cr-salen catalyst was developed. Kinetic studies showed that the oxidation of Cr­(III) to Cr­(V) is the rate-determining step of the reaction. In addition, experimental stoichiometric analysis showed that a high valent Cr­(V) species is the active catalyst for this process. The selectivity of the reaction was found to be determined by the cross-coupling carbon–carbon bond forming reaction, rather than any precoordination species. It appears that the lowest energy cross-coupling pathway requires a lesser degree of electronic reorganization in its transition state vs the lowest energy homocoupling pathway. This result was supported by stoichiometric Cr­(V) kinetics, 13C kinetic isotope effects, and density functional theory (DFT) calculations. The understanding of the full landscape of this reaction allowed us to develop a general analysis to predict the regioselectivity of the cross-coupling reaction.