Carbon dioxide/propylene oxide coupling reaction catalyzed by chromium salen complexes

被引:29
作者
Niu, Yongsheng [1 ,2 ]
Zhang, Wanxi [2 ]
Li, Hongchun [1 ,2 ]
Chen, Xuesi [1 ]
Sun, Jingru [1 ]
Zhuang, Xiuli [1 ]
Jing, Xiabin [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Grad Sch, Changchun 130022, Peoples R China
[2] Jilin Univ, Key Lab Automobile Mat, Minist Educ, Coll Mat Sci & Engn, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide; Propylene oxide; Alternating copolymerization; ZEOLITE-BASED CATALYSTS; PROPYLENE-OXIDE; ALTERNATING COPOLYMERIZATION; CYCLIC CARBONATES; CYCLOHEXENE OXIDE; PHOSPHINE ADDUCTS; MILD CONDITIONS; CO2; ACTIVATION; DIOXIDE; EPOXIDES;
D O I
10.1016/j.polymer.2008.11.008
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 chromium/Schiff base complexes N,N'-bis(salicylidene)-1,2-phenylenediamino chromium(III) X were prepared and employed for the alternating copolymerization of carbon dioxide with racemic propylene oxide in the presence of (4-dimethylamino)pyridine. The effect of the complex structure and reaction conditions on the catalytic activity, the poly(propylene carbonate)/cyclic carbonate (PPC/PC) selectivity, and the polymer head-to-tail linkages was examined. The experiments indicated that N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-phenylenediamino chromium(III) (NO3) exhibited the highest PPC/PC selectivity as well as polymer head-to-tail linkages and N,N'-bis(3,5-dichlorosalicylidene)-1,2-phenylenediimino chromiu(III) (NO3) possessed the highest catalytic activity among these chromium/Schiff base complexes. The structure of the produced copolymer was characterized by the IR, H-1 NMR, and C-13 NMR measurements. Almost 100% carbonate content of the resulting polycarbonate were obtained with the help of these effective catalyst systems under facile conditions. Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:441 / 446
页数:6
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