Catalytic ring-attachment isomerization and dealkylation of diethylbenzenes over halide clusters of group 5 and group 6 transition metals

Abstract

A molybdenum halide cluster, (H 3O) 2[(Mo 6Cl 8)Cl 6]·6H 2O, possessing an octahedral metal framework was used as a catalyst in a gas flow reactor under 1 atm of hydrogen. On reaction of p-diethylbenzene, dehydrogenation to ethylstyrene proceeded selectively at 300 °C. At 400 °C, mutual interconversion of o-, m-, and p-diethylbenzenes proceeded selectively. The ethyl group migrated by an intramolecular 1,2-shift mechanism without yielding disproportionation products. Niobium and tungsten chloride clusters with the same metal framework were also active catalysts for the isomerization of p-diethylbenzene. All the reactions resulted in appreciable yields of dealkylation products. The catalytic activity for isomerization can be ascribed to acid sites on the cluster surface, and the catalytic activity for dealkylation, to the metallic nature of the framework metal.