Synthesis, characterization and ethylene polymerisation of 9,10-phenanthrenequinone-based nickel(II)-α-diimine complexes

被引:47
作者
Li, Lidong
Jeon, Manseong
Kim, Sang Youl
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Polyolefin Mat Res Ctr, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Sch Mol Sci BK21, Taejon 305701, South Korea
关键词
Nickel complex; 9,10-Phenanthrenequinone; Polyethylene (PE); OLEFIN POLYMERIZATION; ALPHA-OLEFINS; COORDINATION POLYMERIZATION; CATALYTIC POLYMERIZATION; LIVING POLYMERIZATION; METAL CATALYSTS; COPOLYMERIZATION; WATER; ACTIVATION; IRON;
D O I
10.1016/j.molcata.2009.01.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two 9,10-phenanthrenequinone-based alpha-diimine ligands (N,N'Z, N,N'E)-N,N'-(phenanthrene-9,10-diylidene)bis(2,6-dimethylaniline) (1) and (Z)-2,6-dimethyl-N-((E)-10-methylbenzo[f]phenanthro[10,1-bc]azepin-8(14H)-ylidene)aniline (2), were prepared by condensation of 2,6-dimethylaniline and 9,10-phenanthrenequinone in the presence of the TiCl4/1,4-diazabicyclo[2.2.2]octine catalytic system in a one-pot reaction. It was experimentally demonstrated that a reaction temperature increase favors the formation of ligand 2. Nickel dibromide complexes 3 and 4 were synthesized from ligands 1 and 2, respectively, and both showed high productivities as catalysts for polymerisation of ethylene. Complex 3 yielded ultrahigh molecular weight polyethylenes at low temperature (e.g., 1.26 x 10(6) g/mol at -15 C), which are significantly higher than those Produced by the corresponding 2.3-butanedione- or acenaphthenequinone-based alpha-diimine nickel complexes. Complex 4 produced polyethylenes with relatively lower molecular weights, when compared to 3. It was shown that the catalyst Structure and reaction conditions, like the reaction temperature and concentration of activator (MAO), have Substantial influence on the polymerisation activities and Molecular weights and microstructures of the resulting polymers. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:110 / 116
页数:7
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