Vinylic and ring-opening metathesis polymerization of norbornene with bis(β-ketoamine) cobalt complexes

被引:36
作者
Bao, F
Lü, XQ
Gao, HY
Gui, GQ
Wu, Q [1 ]
机构
[1] Zhongshan Univ, Inst Polymer Sci, Guangzhou 510275, Peoples R China
[2] Cent China Normal Univ, Coll Chem, Wuhan 430079, Peoples R China
[3] Zhongshan Univ, Sch Chem & Chem Engn, Guangzhou 510275, Peoples R China
关键词
beta-ketoamine; cobalt complexes; catalysts; crystal structures; norbornene; ROMP; vinylic polymerization;
D O I
10.1002/pola.21036
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cobalt complexes 1-4 bearing NO-chelate ligands based on condensation products of 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone with aniline, o-methylaniline, alpha-naphthylamine, and p-nitroaniline, respectively, were synthesized, and the structures of 1 and 4 were characterized by single-crystal X-ray diffraction analyses. The bis(beta-ketoamine) cobalt complexes could act as moderately active catalyst precursors for norbornene polymerization with the activation of methylaluminoxane. This catalytic reaction proceeded mainly through a vinyl-type polymerization mechanism. H-1 NMR and IR showed that in all cases, a small amount of double bonds raised from ring-opening metathesis polymerization (ROMP) was present in the polymerization products. The variation of the polymerization conditions affected the ROMP unit ratio in the polynorbornenes. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:5535 / 5544
页数:10
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