Rhodium(III) complexes containing C4-bound N-heterocyclic carbenes:: Synthesis, coordination chemistry, and catalytic activity in transfer hydrogenation

Direct metalation of C2-protected diimidozolium salts with RhCl3 or [RhC](cod)12 and KI afforded a series of new rhodium(III) complexes with abnormally C4-bound, cis-chelating NHC ligands. The complexes were isolated as dimetallic species containing two (mu(2)-I)(3)-bridged rhodium(III) centers. In the presence of coordinating ligands such as CH3CN, PPh3, or dppe, the dimeric structure is readily cleaved and yields monometallic complexes. Crystallographic analysis of representative structures indicates a higher trans influence of abnormally C4-bound carbenes as compared to normal NHCs. The exceptionally strong donor ability of carbenes in such a C4 coordination mode increases the catalytic activity of the rhodium center and allows for efficient transfer hydrogenation of ketones in iPrOH/KOH.