4.5 Article

Synthesis, structure, and catalytic activity of rhodium complexes with new chiral binaphthyl-based NHC-ligands

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 696, Issue 23, Pages 3714-3720

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2011.08.015

Keywords

Carbene complex; Rhodium; Binaphthyl ligand; Asymmetric hydrosilylation

Funding

  1. National Natural Science Foundation of China [20872062, 20972018, 21074013, 21172022]
  2. Program for New Century Excellent Talents in University [NCET-10-0253]
  3. Beijing Municipal Commission of Education

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Three new chiral NHC-rhodium complexes have been prepared from the reactions between [Rh(COD)Cl](2), NaOAc, KI, and dibenzimidazolium salts 3, 4 or 5, which are derived from (S)-2,2'-diamino-1,1'-binaphthyl. The steric and electronic effects of the ligand play an important role in the complex formation. For example, treatment of pyridine substituted dibenzimidazolium salts 3 or 4 with 0.5 equiv of [Rh(COD)Cl](2) in the presence of NaOAc and KI in CH3CN at 85 degrees C gives the chiral Rh(III) complexes 6 and 7, respectively. However, under similar reaction conditions, pyridine-N-oxide substituted dibenzimidazolium salt 5 affords a binuclear Rh(I) complex 8. All compounds have been characterized by various spectroscopic techniques, and elemental analyses. The solid-state structures of compounds 4-8 have been further confirmed by X-ray diffraction analyses. Rhodium complexes 6-8 show good catalytic activity for the asymmetric hydrosilylation of acetophenone with moderate ee values. (C) 2011 Elsevier B.V. All rights reserved.

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