二亚胺
阳离子聚合
乙烯
聚合
镍
催化作用
高分子化学
甲基铝氧烷
化学
齿合度
材料科学
光化学
有机化学
聚合物
茂金属
金属
作者
Igor E. Soshnikov,Nina V. Semikolenova,Konstantin P. Bryliakov,Evgenii P. Talsi
出处
期刊:Catalysts
[MDPI AG]
日期:2021-11-17
卷期号:11 (11): 1386-1386
被引量:8
标识
DOI:10.3390/catal11111386
摘要
Nickel(II) complexes with bidentate N,N-α-diimine ligands constitute a broad class of promising catalysts for the synthesis of branched polyethylenes via ethylene homopolymerization. Despite extensive studies devoted to the rational design of new Ni(II) α-diimines with desired catalytic properties, the polymerization mechanism has not been fully rationalized. In contrast to the well-characterized cationic Ni(II) active sites of ethylene polymerization and their precursors, the structure and role of Ni(I) species in the polymerization process continues to be a “black box”. This perspective discusses recent advances in the understanding of the nature and role of monovalent nickel complexes formed in Ni(II) α-diimine-based ethylene polymerization catalyst systems.
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