Synthesis and Investigation of Homo- and Heterobimetallic Ruthenium Olefin Metathesis Catalysts Exhibiting Increased Activities

Abstract

The previously reported ruthenium carbenes (PCy3)2Cl2RuCHR (R = CHCPh2 (1a), Ph (1b)) react with the bridged-chloride dimers [(p-cymene)RuCl2]2, [(p-cymene)OsCl2]2, and [(tBu2Cp)RhCl2]2 to quantitatively form the bimetallic, bridged-chloride ruthenium carbenes 2a,b, 4a,b, and 6a,b and 1 equiv of each corresponding piano-stool complex. In the ring-opening metathesis polymerization of 1,5-cyclooctadiene, catalyst activity was found to increase in the order M = Ru < Os < Rh for the ancillary metal centers, with all of the bimetallic catalysts having higher activities than 1a,b. The kinetics of ROMP of the derivatized norbornene 9 were studied using catalyst 2a, and the data support an associative mechanism of olefin metathesis, contrary to the mechanism of olefin metathesis proposed for the parent catalysts 1a,b.