Synthesis and characterization of chiral mono N-heterocyclic carbene-substituted rhodium complexes and their catalytic properties in hydrosilylation reactions

Different chiral mono-substituted N-heterocyclic carbene complexes of rhodium were prepared, starting from [Rh(COD)Cl]2 (COD = cyclooctadiene) by addition of free N-heterocyclic carbenes (NHC), or an in-situ deprotonation of the corresponding iminium salt. All new complexes were characterized by spectroscopy methods. In addition, the structures of chloro(η4-1,5-cyclooctadiene)(1,3-di-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl] imidazolin-2-ylidene)rhodium(I) (5a), chloro(η4-1,5-cyclooctadiene)(1,3-di-[(1R,2S,5R)-2-isopropyl-5-menthylcyclohex-1-yl]imidazol-2-ylidene)rhodium(I) (5b) and chloro(η4-1,5-cyclooctadiene)(1,3-di-[(2R,4S,5S)-2-methyl-4-phenyl-1,3-dioxacyclohex-5-yl]imidazolin-2-ylidene)rhodium(I) (5i) were analyzed by DFT-calculations. The enantioselective hydrosilylation of acetophenone, ethylpyruvate and n-propylpyruvate with diphenylsilane and hydrolysis was carried out with chiral C2-symmetrical mono-substituted N-heterocyclic carbene rhodium complexes giving for the first time an enantioselective excess of up to 74% ee in the case of the n-propylpyruvate.

Graphical abstractChiral mono-substituted N-heterocyclic carbene complexes of rhodium were prepared, analyzed by DFT-calculations and used for the enantioselective hydrosilylation of acetophenone, ethylpyruvate and n-propylpyruvate with diphenylsilane giving for the first time an enantioselective excess of up to 74% ee with chiral C2-symmetrical mono substituted N-heterocyclic carbene rhodium complexes.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► We prepared chiral mono-substituted N-heterocyclic carbene complexes of rhodium ► High enantioselective selectivities of 74% ee for hydrosilylation reactions ► Strong donors as ligands for rhodium complexes. ► DFT-calculations for conformation of chiral-rhodium complexes