4.7 Article

Highly regio- and stereo-selective copolymerization of CO2 with racemic propylene oxide catalyzed by unsymmetrical (S,S,S)-salenCo(III) complexes

Journal

SCIENCE CHINA-CHEMISTRY
Volume 53, Issue 8, Pages 1646-1652

Publisher

SCIENCE PRESS
DOI: 10.1007/s11426-010-4049-1

Keywords

carbon dioxide; propylene oxide; polycarbonate; stereochemistry; asymmetric catalysis polymerization; kinetic resolution

Funding

  1. National Natural Science Foundation of China [20634040]
  2. National Basic Research Program of China (973 Program) [2009CB825300]
  3. Outstanding Young Scientist Foundation of the National Natural Science Foundation of China [20625414]

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A novel unsymmetrical (S,S,S)-salen ligand bearing a derived chiral-BINOL was synthesized by the reaction of the condensation product of (1S,2S)-1,2-diaminocyclohexane mono(hydrogen chloride) with 3-adamanyl-5-tert-butyl-2-hydroxybenzalde-hyde and 3-formoyl-2-hydroxy-2'-alkyloxy-1,1'-binaphthyl, which originated from (S)-1,1'-bi-2-naphthol via a four-step reaction. The cobalt complexes of this ligand, in conjunction with a nucleophilic cocatalyst, exhibited excellent activity in catalyzing asymmetric, regio- and stereo-selective copolymerization of CO2 and racemic propylene oxide. The highest record of kinetic resolution coefficient (K-rel) was obtained with the use of binary catalyst system consisting of (S,S,S)-salenCo(III) complex 1c and bulky bis(triphenylphosphine)-iminium chloride (PPNCl). The resulting poly(propylene carbonate)s have more than 99% carbonate linkages and more than 98% head-to-tail content.

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