Reversible coordinative chain transfer polymerization of isoprene and copolymerization with ε-caprolactone by neodymium-based catalyst

被引:51
作者
Wang, Feng [1 ,2 ]
Zhang, Chun-yu [1 ]
Hu, Yan-ming [3 ]
Jia, Xiang-yu [1 ,2 ]
Bai, Chen-xi [1 ]
Zhang, Xue-quan [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Res Ctr High Performance Synthet Rubber, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] Dalian Univ Technol, Sch Chem Engn, Dept Polymer Sci & Engn, Dalian 116012, Peoples R China
关键词
Coordinative chain transfer polymerization; Isoprene polymerization; Neodymium-based catalyst; RING-OPENING POLYMERIZATION; BLOCK COPOLYMERIZATION; LIVING POLYMERIZATION; STEREOSPECIFIC POLYMERIZATION; MONOMER COPOLYMERIZATION; DIBLOCK COPOLYMERS; POLAR MONOMERS; ETHYLENE; BUTADIENE; ALUMINUM;
D O I
10.1016/j.polymer.2012.10.044
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Coordinative chain transfer polymerization (CCTP) of isoprene was investigated by using the typical Ziegler-Natta catalytic system [Nd(Oi-Pr)(3)/Al(i-Bu)(2)H/Me2SiCl2] with Al(i-Bu)(2)H as cocatalyst and chain transfer agent (CFA). The catalyst system exhibited high catalytic efficiency for the reversible CCTP of isoprene and yielded 6-8 polymer chains per Nd atom due to the high chain transfer ability of Al(i-Bu)(2)H. The narrow molecular weight distribution (M-w/M-n = 1.22-1.45) of the polymers, the good linear relationship between the M-n and yield of the polymer, and the feasible seeding polymerization of isoprene indicated the living natures of the catalyst species. Moreover, the living Nd-polyisoprene active species could further initiate the ring-opening polymerization of polar monomer (epsilon-caprolactone) to afford an amphiphilic block copolymer consisting of cis-1,4-polyisoprene and poly(epsilon-caprolactone) with controllable molecular weight and narrow molecular weight distribution. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6027 / 6032
页数:6
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