Synthesis, Characterization, and Catalytic Behaviors in Isoprene Polymerization of Pyridine-Oxazoline-Ligated Cobalt Complexes

被引:2
作者
Hao, Xiuge [1 ]
Liu, Jin-Kui [1 ]
Zhuo, Weize [1 ]
Zheng, Jiajing [1 ]
Hao, Xin-Qi [1 ]
Gong, Jun-Fang [1 ]
Jiang, Hui [1 ]
Song, Mao-Ping [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
pyridine-oxazoline ligand; cobalt catalyst; isoprene polymerization; isoprene; SYNDIOTACTIC 1,2-POLYBUTADIENE; BUTADIENE POLYMERIZATION; ETHYLENE; LIGANDS; BEARING; PROGRESS; NICKEL; SYSTEM; IRON;
D O I
10.3390/polym16050578
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 family of pyridine-oxazoline-ligated cobalt complexes L2CoCl2 3a-h were synthesized and characterized. Determined via single-crystal X-ray diffraction, complexes 3a and 3d, ligated by two ligands, displayed a distorted tetrahedral coordination of a cobalt center. The X-ray structure indicated the pyridine-oxazoline ligands acted as unusual mono-dentate ligands by coordinating only to Noxazoline. Upon activation with AlEt2Cl (diethylaluminum chloride), these cobalt complexes all exhibited high catalytic activity (up to 2.5 x 106 g center dot molCo-1 center dot h-1), affording cis-1,4-co-3,4-polyisoprene with molecular weights of 4.4-176 kg mol-1 and a narrow of 1.79-3.42, suggesting a single-site nature of the active sites. The structure of cobalt catalysts and reaction parameters, especially co-catalysts and the reaction temperature, all have significant influence on the polymerization activity but not on the microstructure of polyisoprene.
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页数:12
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