Irreversible cleavage of a carbene–rhodium bond in Rh- N-heterocyclic carbene complexes: implications for catalysis

Abstract

Despite the generally accepted belief that carbene–metal bonds are strong and do not dissociate, the reaction of Rh- N-heterocyclic carbene complexes with triphenylphosphine in dichloroethane was determined to take place via cleavage of the Rh–carbene bond. The products of this reaction are Wilkinson’s catalyst and a bisimidazolium salt derived from reaction between dichloroethane and two equivalents of the carbene. The implications of this reaction for catalysis are significant since the carbene complex shows lower activity than Wilkinson’s catalyst in hydrogenation reactions. In non-halogenated solvents, the catalyst shows higher stability, such that the rate of exchange with free phosphine could be measured, and was determined to be ca. 10 times slower than in Wilkinson’s catalyst.