High cis-1,4 polyisoprene or cis-1,4/3,4 binary polyisoprene synthesized using 2-(benzimidazolyl)-6-(1-(arylimino)ethyl)pyridine cobalt(II) dichlorides

被引:26
作者
He, Aihua [1 ]
Wang, Geng [1 ]
Zhao, Weizhen [2 ,3 ]
Jiang, Xiubo [1 ]
Yao, Wei [1 ]
Sun, Wen-Hua [2 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Sch Polymer Sci & Engn, Key Lab Rubber Plast, Minist Educ,Shandong Prov Key Lab Rubber Plast, Qingdao 266042, Peoples R China
[2] Chinese Acad Sci, Key Lab Engn Plast, Inst Chem, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100190, Peoples R China
关键词
cis-1,4 polyisoprenes; cis-1,4/3,4 binary polyisoprenes; cobalt pre-catalyst; late transition metal complexes; BUTADIENE POLYMERIZATION BEHAVIOR; STEREOSPECIFIC CATALYST; CONJUGATED DIENES; COMPLEXES; COPOLYMERIZATION; CHEMOSELECTIVITY; POLYBUTADIENE; PROPYLENE; LIGAND;
D O I
10.1002/pi.4490
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyisoprene (PI) with a high content of cis-1,4 (up to 95%) or cis-1,4/3,4 binary structures was synthesized using a cobalt system in toluene. The cobalt system, which exhibited high activities (up to 3.50x10(6) g PI(mol Co)(-1)h(-1)), contained a series of 2-(benzimidazolyl)-6-(1-(arylimino)ethyl)pyridine cobalt(II) dichlorides activated with ethylaluminium sesquichloride. The nature of the ligands and the reaction conditions significantly affected both the catalytic performance of the cobalt complexes as well as the structures of the resultant PI. The stereospecific polymerization of isoprene could be tuned via changing either the co-catalyst or solvent: for example, increased content of 3,4 PI (up to 36.6%) was achievable in heptane in the presence of diethylaluminium chloride. Sequence distribution analysis by C-13 NMR spectroscopy indicated that most 3,4 units occurred randomly in the PI chains. (c) 2013 Society of Chemical Industry
引用
收藏
页码:1758 / 1766
页数:9
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