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Hyperbranched-linear polyethylene block polymers constructed with chain blocks of hybrid chain topologies via one-pot stagewise chain walking ethylene 'living' polymerization

机译:通过一锅式逐步链走乙烯“活性”聚合反应,由杂化链拓扑结构的链嵌段构成的超支化线性聚乙烯嵌段聚合物

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摘要

We demonstrate in this article the facile synthesis of a novel range of "treelike" polyethylene block polymers constructed uniquely with chain blocks of hybrid hyperbranched-linear chain topologies from sole ethylene stock. Though chemically identical, the blocks in the polymers are featured with distinctly different chain topologies, varying from hyperbranched to linear. This synthesis is achieved uniquely through one-pot stagewise chain walking ethylene "living" polymerization with a Pd-diimine catalyst, [(ArNC(Me)-(Me)CNAr)Pd(CH_3)(N≡CMe)]~+SbF _6~- (Ar = 2,6-(iPr)_2C_6H_3) (1), under varying conditions. It takes advantage of the combined outstanding features of the Pd-diimine catalyst in ethylene polymerization the "living" polymerization behavior at a broad range of ethylene pressure and temperature and the capability of topology tuning by changing both parameters. In this stagewise "living" polymerization technique, the polymerization condition (ethylene pressure and temperature) is varied from stage to stage to grow blocks of different desired topologies while with maintained "living" behavior. With this technique, diblock polymers, containing a hyperbranched first block and a linear second block with controllable narrow-distributed sizes, have been obtained through two-stage polymerizations using the growth order of "hyperbranched-first" with the first stage at 1 atm/15 °C and the second stage at 27 atm/5 °C. The distinct block structure in these diblock polymers is verified based on the fact that their intrinsic viscosity data follow consistently the combination rule found with conventional diblock polymers. In addition, the synthesis of triblock polymers, composed of a hyperbranched first block, a medium-compact second block, and a linear third block, is also demonstrated through three-stage polymerization involving the first stage at 1 atm/15 °C, the second at 3 atm/15 °C, and the third at 27 atm/5 °C.
机译:我们在本文中证明了从单一乙烯原料中轻松合成新型“树状”聚乙烯嵌段聚合物的方法,该聚合物独特地构建有杂化超支化-线性链拓扑结构的链嵌段。尽管在化学上相同,但是聚合物中的嵌段具有明显不同的链拓扑结构,从超支化到线性变化。这种合成是通过使用Pd-二亚胺催化剂[(ArNC(Me)-(Me)CNArAr)Pd(CH_3)(N≡CMe)]〜+ SbF _6单步逐步链走乙烯“活性”聚合来实现的〜-(Ar = 2,6-(iPr)_2C_6H_3)(1),在不同条件下。它利用了Pd-二亚胺催化剂在乙烯聚合中综合的突出特征,在宽广的乙烯压力和温度范围内的“活性”聚合行为以及通过改变两个参数进行拓扑调整的能力。在这种阶段性的“活性”聚合技术中,聚合条件(乙烯压力和温度)在各个阶段之间变化,以生长具有不同期望拓扑的嵌段,同时保持“活性”行为。通过这种技术,使用“超支化优先”的生长顺序,第一步为1 atm / m2的生长顺序,通过两步聚合反应,获得了含有超支化的第一嵌段和线性第二嵌段且可控制的窄分布尺寸的二嵌段聚合物。 15°C,第二阶段温度为27 atm / 5°C。基于以下事实验证了这些二嵌段聚合物中独特的嵌段结构:它们的特性粘度数据始终遵循常规二嵌段聚合物发现的组合规则。此外,三嵌段聚合物的合成还包括三步聚合反应,该反应由超支化的第一个嵌段,中等致密的第二个嵌段和线性的第三个嵌段组成,该过程涉及第一步在1 atm / 15°C的条件下进行。第二个温度为3 atm / 15°C,第三个温度为27 atm / 5°C。

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