首页> 外文期刊>Macromolecular chemistry and physics >Polymerization of 4-methyl-1,3-pentadiene with catalysts based on cyclopentadienyl titanium chlorides: Effect of anti/syn isomerism of the allylic group on the chemo selectivity and the role of backbiting coordination in 1,3-diene polymerization
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Polymerization of 4-methyl-1,3-pentadiene with catalysts based on cyclopentadienyl titanium chlorides: Effect of anti/syn isomerism of the allylic group on the chemo selectivity and the role of backbiting coordination in 1,3-diene polymerization

机译:用基于环戊二烯基氯化钛的催化剂聚合4-甲基-1,3-戊二烯:烯丙基的抗/同位异构体对化学选择性的影响和回位配位在1,3-二烯聚合中的作用

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摘要

Homopolymerization of 4-methyl-1,3-pentadiene (MP) and copolymerization of 4-methyl-1,3-pentadiene with alkenes (ethylene, 1-pentene, 4-methyl-1-pentene) were performed to investigate the effect of the so-called backbiting coordination on the chemoselectivity of 1,3-diene polymerization. Three homogeneous catalyst systems were used: CpTiCl3-MAO, Cp2TiCl2-MAO and Cp2TiCl-MAO. Backbiting coordination is possible with the first catalyst, but not with the other two. The three catalysts gave similar results, which indicates that backbiting has no effect on the polymerization chemoselectivity, contrary to what has been reported in recent literature. An interpretation is presented for the formation of 1,4 units in MP/alkene copolymers. This interpretation is based on the fact that allyl groups have predominantly a syn configuration in MP homopolymerization, whereas allyl groups of anti configuration are formed in MP/alkene copolymerization. The role of backbiting in diene polymerization is discussed.
机译:进行了4-甲基-1,3-戊二烯(MP)的均聚和4-甲基-1,3-戊二烯与烯烃(乙烯,1-戊烯,4-甲基-1-戊烯)的共聚反应,研究了所谓的1,3-二烯聚合化学选择性的逆位配位。使用了三种均相催化剂体系:CpTiCl3-MAO,Cp2TiCl2-MAO和Cp2TiCl-MAO。使用第一个催化剂可以进行回位协调,但不能使用其他两个催化剂。这三种催化剂给出了相似的结果,这表明与最新文献报道的相反,回位对聚合的化学选择性没有影响。提出了在MP /烯烃共聚物中形成1,4单元的解释。该解释基于以下事实:烯丙基在MP均聚中主要具有顺式构型,而反构型的烯丙基在MP /烯烃共聚中形成。讨论了咬位在二烯聚合中的作用。

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