Promoting terminal olefin metathesis with a supported cationic molybdenum imido alkylidene n-heterocyclic carbene catalyst

Silica-supported cationic Mo-imido alkylidene Nheterocyclic carbene catalysts, prepared by surface organometallic chemistry, display contrasting olefin metathesis activity for terminal and internal olefins. The high metathesis activity towards terminal alkenes is attributed to the strong s-donating property of the NHC ancillary ligand, which disfavors the formation of the parent square-planar metallacyclobutane, an off-cycle reaction intermediate resulting from the reaction with ethylene, one of the metathesis products. This tailored ligand environment also allowed the first trigonal bipyramidal (TBP) metallacyclobutane reaction intermediate for supported Mometathesis catalysts to be identified.