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Alternating copolymerization of carbon dioxide and propylene oxide by single-component cobalt salen complexes with various axial group
被引:39
作者:
Liu, Binyuan
[1
]
Zhao, Xin
[1
]
Guo, Hongfei
[1
]
Gao, Yanhao
[1
]
Yang, Min
[1
]
Wang, Xianhong
[2
]
机构:
[1] Hebei Univ Technol, Inst Polymer Sci & Engn, Tianjin 300130, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
来源:
关键词:
Carbon dioxide;
Propylene oxide;
Copolymerization;
BINARY CATALYST SYSTEMS;
POLY(PROPYLENE CARBONATE);
CO2/EPOXIDE COPOLYMERIZATION;
ALIPHATIC POLYCARBONATES;
STEREOCHEMISTRY CONTROL;
(SALEN)CRX COMPLEXES;
CYCLOHEXENE OXIDE;
MILD CONDITIONS;
ZINC GLUTARATE;
CO2;
D O I:
10.1016/j.polymer.2009.08.034
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
A series of single-component cobalt salen complexes, N,N'-bis(salicylidene)-1,2phenylenediamino cobaltIII X(X = Cl (1a), Br (1b), NO3 (1c), CF3COO (1d), BF4 (le), and N3 (If)) (SalphCoX), were prepared for alternating copolymerization of carbon dioxide and propylene oxide(PO) under mild condition. The axial anion X group of the SalenphCoX played important role in tailoring the catalytic activity, polymeric/cyclic carbonate selectivity, as well as stereochemistry of carbonate unit sequence in the polymer chain. SalenphCoX with an electron-withdrawing axial X group (complex 1c) was an ideal catalyst for the copolymerization of CO2 and PO to selectively produce polycarbonate with similar to 99% carbonate linkage and over 81% head-to-tail structure. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:5071 / 5075
页数:5
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