Living Coordination Polymerization of Alkylallenes by π-Allylnickel Catalyst: Observation of an Extremely High Polymerizability of 1,2-Cyclononadiene

Living Coordination Polymerization of Alkylallenes by π-Allylnickel Catalyst: Observation of an Extremely High Polymerizability of 1,2-Cyclononadiene
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π-烯丙基镍催化剂对亚烷基的活性配位聚合:观察到 1,2-环壬二烯的极高聚合性

DOI:
10.1246/cl.1997.1187
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发表时间:
1997
期刊:
影响因子:
1.6
通讯作者:
T. Endo
T. Endo
中科院分区:
化学4区
文献类型:
--
作者:
Koji Takagi;I. Tomita;T. Endo

文献摘要

被引文献

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研究了[(π-烯丙基)NiOCOCF_3]_2与环状联烯的配位聚合,以高产率制备窄分子量分布的聚合物。聚合反应以活性机理进行,所得聚合物的分子量与单体投料比呈线性关系。特别地,1,2-环壬二烯(即,具有显著环应变的单体)与无环单体相比进行得非常快。
The coordination polymerization of cyclic allenes by [(π-allyl)NiOCOCF3]2 was investigated to produce polymers with narrow molecular weight distributions in high yields. The polymerization proceeded in a living mechanism, and the molecular weight of the resulting polymer had a linear relationship with the monomer feed ratio. Especially, the polymerization of 1,2-cyclononadiene (i.e., a monomer with substantial ring strain) proceeded dramatically fast compared with acyclic monomers.