Equilibrium constants and kinetics of carbon monoxide insertion in alkyl complexes of ruthenium(II)

Abstract

The equilibrium constants of the reaction of cis, trans-[Ru(CO) 2(PMe 3) 2(CH 3)I] ( Mc) with carbon monoxide to give cis, trans[Ru(CO) 2(PMe 3) 2 (COMe)i] ( Ac) and trans, trans[Ru(CO) 2(PMe 3) 2(COMe)I] ( At) were measured at various temperatures in toluene. The thermodynamic parameters are compared with those obtained for the isoelectronic complexes of iron, and the trend is discussed. The kinetics of the carbonylation reaction of Mc, as well as those of the inverse decarbonylation reaction of At were measured. The kinetics of the carbonylation of the new complex trans, trans-[Ru(CO) 2(PMe 3) 2(CH 3)I] ( Mt) were also investigated. All the results afford further support to the previously proposed CO insertion mechanism occurring via methyl migration. The comparison of these kinetic results with those of isoelectronic complexes of iron indicates that ruthenium is more reactive than iron, which is reflected by its greater aptitude to act as catalyst in many processes.