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A New Synthesis Strategy on Styrene-Butadiene Di-Block Copolymer Containing High cis-1,4 Unit Via Transfer of Anionic to Coordination Polymerization

机译:阴离子转移到配位聚合制备高顺式1,4单元苯乙烯-丁二烯二嵌段共聚物的合成新策略

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摘要

A novel synthesis strategy on styrene-butadiene di-block copolymer (PS-b-PB) with high cis-1,4 unit content was developed, based on a transfer technique from anionic to coordination polymerization. Firstly, the styrene monomer was initiated by n-butyllithium (Li) utilizing anionic polymerization at 50 °C, which resulted in a macromolecular alkylating initiator (PSLi). Secondly, PSLi was aged with nickel naphthenate (Ni) and boron trifluoride etherate (B) for obtaining a complex catalyst system (Ni/PSLi/B). Then, Ni/PSLi/B was applied to initiate the butadiene (Bd) polymerization. Following this new strategy, a series of PS-b-PBs were successfully synthesized. The experimental results indicated that under the molar ratio combination of [Li]/[Ni] = 5 and [B]/[Li] = 1, styrene-butadiene di-block copolymers could be easily achieved with high cis-1,4 unit content (>97%) and controlled molecular weight as well as narrow molecular weight distribution (Mw/Mn < 1.5). Furthermore, the copolymer’s block ratio could also be effectively controlled by controlling the two components’ monomer feed ratio.
机译:基于从阴离子到配位聚合的转移技术,开发了一种高顺式1,4单元含量的苯乙烯-丁二烯二嵌段共聚物(PS-b-PB)的合成策略。首先,利用正丁基锂(Li)在50°C下通过阴离子聚合引发苯乙烯单体,从而生成大分子烷基化引发剂(PSLi)。其次,将PSLi与环烷酸镍(Ni)和三氟化硼醚化物(B)进行时效处理,以获得复杂的催化剂体系(Ni / PSLi / B)。然后,应用Ni / PSLi / B引发丁二烯(Bd)聚合。遵循这一新策略,成功合成了一系列PS-b-PB。实验结果表明,在[Li] / [Ni] = 5和[B] / [Li] = 1的摩尔比组合下,高顺式1,4单元可轻松实现苯乙烯-丁二烯二嵌段共聚物含量(> 97%)和可控制的分子量以及窄的分子量分布(Mw / Mn <1.5)。此外,还可以通过控制两种组分的单体进料比来有效控制共聚物的嵌段比。

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