Stereospecific polymerization of 1,3-butadiene catalyzed by cobalt complexes bearing N-containing diphosphine PNP ligands

被引:38
|
作者
Chen, Lin [1 ]
Ai, Pengfei [1 ]
Gu, Jianming [2 ]
Jie, Suyun [1 ]
Li, Bo-Geng [1 ]
机构
[1] Zhejiang Univ, Dept Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
Cobalt; Phosphine; 1,3-Butadiene; Polymerization; CO-BASED CATALYST; RAY CRYSTAL-STRUCTURE; ETHYLENE OLIGOMERIZATION; BUTADIENE POLYMERIZATION; STRUCTURAL-CHARACTERIZATION; CHELATING DIPHOSPHINES; LIVING POLYMERIZATION; DIENE POLYMERIZATION; TRANSITION-METALS; CONJUGATED DIENES;
D O I
10.1016/j.jorganchem.2012.05.051
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of cobalt complexes bearing N-containing diphosphine PNP ligands has been synthesized and characterized. The nature of the ligand structure affects the binding of the ligand to the cobalt center and determines the coordination geometry of the cobalt complexes. All the complexes have been employed to catalyze the polymerization of 1,3-butadiene, in combination with methylaluminoxane (MAO) or ethylaluminum sesquichloride (EASC) as the cocatalyst. Both the nature of the ligand and the type of cocatalyst had a remarkable influence on the polymerization activity, microstructure and molecular weight of the resulting polymers. The [Co]/MAO catalytic systems resulted in relatively lower conversions of butadiene and cis-1,4 contents in the polymers than the corresponding [Co]/EASC catalytic systems. Upon activation with EASC, the polymerization behaviors of the catalytic systems were also affected by the reaction parameters. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 61
页数:7
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