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Highly regio- and stereo-selective copolymerization of CO2 with racemic propylene oxide catalyzed by unsymmetrical (S,S,S)-salenCo(III) complexes
被引:60
作者:
Ren WeiMin
Zhang WenZhen
Lu XiaoBing
[1
]
机构:
[1] State Key Lab Fine Chem, Dalian 116012, Peoples R China
基金:
中国国家自然科学基金;
关键词:
carbon dioxide;
propylene oxide;
polycarbonate;
stereochemistry;
asymmetric catalysis polymerization;
kinetic resolution;
CARBON-DIOXIDE;
ALTERNATING COPOLYMERIZATION;
CO2/EPOXIDE COPOLYMERIZATION;
STEREOCHEMISTRY CONTROL;
SALEN COMPLEXES;
EPOXIDES;
SELECTIVITY;
MECHANISM;
SYSTEMS;
D O I:
10.1007/s11426-010-4049-1
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
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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页码:1646 / 1652
页数:7
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