Synthesis and X-ray structures of rhodium complexes with new chiral biaryl-based NHC-ligands

A new series of chiral NHC–rhodium complexes has been prepared from the reactions between [Rh(COD)Cl]2, NaOAc, KI and dibenzimidazolium salt 4a or monobenzimidazolium salts 4b–d, which are derived from chiral 2,2′-diamino-6,6′-dimethyl-1,1′-biphenyl, 2,2′-diamino-1,1′-binaphthyl or 6,6′-dimethyl-2-amino-2′-hydroxy-1,1′-biphenyl. The steric and electronic effects of the ligand play an important role in the complex formation. For example, treatment of chiral monobenzimidazolium salt 4b (with a NMe2 group) with 0.5 equiv of [Rh(COD)Cl]2 in the presence of NaOAc and KI in CH3CN at reflux gives a chiral Rh(I) complex 5b, while chiral monobenzimidazolium salt 4d (with a MeO group) affords a racemic Rh(I) complex 5d. Under similar reaction conditions, treatment of dibenzimidazolium salt 4a with 0.5 equiv of [Rh(COD)Cl]2 in the presence of NaOAc and KI gives a racemic Rh(III) complex 5a, while the dibenzimidazolium salt [C20H12(C7H5N2Me)2]I2 derived from chiral 2,2′-diamino-1,1′-binaphthyl affords a chiral Rh(III) complex [C20H12(C7H4N2Me)2]RhI2(OAc). All compounds have been characterized by various spectroscopic techniques, and elemental analyses. The solid-state structures of the rhodium complexes have been further confirmed by X-ray diffraction analyses.

A new series of chiral NHC–rhodium complexes have been prepared. The steric effect of the ligand plays a key role in the formation of the complexes. The benzimidazolium salt 4b reacts with [Rh(COD)Cl]2 in the presence of NaOAc and KI gives a chiral complex 5b, while 4d affords a racemic complex 5d.Figure optionsDownload as PowerPoint slide