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Copolyethers with controlled structure: Mechanism of formation and microstructure

机译:结构受控的共聚醚:形成机理和微观结构

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摘要

Cationic copolymerization of 3-membered cyclic ethers (oxiranes) with 5-membered cyclic ether (tetrahydrofuran) leads to linear copolyethers containing significant amount of cyclic fraction. When the copolymerization is conducted in the presence of diols, telechelic copolymers are formed by the process in which oxirane is incorporated into copolymer irreversibly by Activated Monomer mechanism, while tetrahydrofuran is incorporated reversibly by Active Chain End mechanism. Thus both kinetic and thermodynamic factors can be used to control the rate of the incorporation of comonomers. Studies of the kinetics of the competing reactions leading to formation of copolymer, studies of copolymer microstructure by C-13-NMR and analysis of the composition of the cyclic fraction, led to the correlation between the copolymer microstructure and the amount of cyclic faction formed. The dependence of the cyclic faction content on the reaction conditions was therefore explained. [References: 11]
机译:3元环醚(oxiranes)与5元环醚(四氢呋喃)的阳离子共聚导致线性共聚醚含有大量的环状部分。当在二醇的存在下进行共聚时,通过螯合环氧乙烷通过活化单体机理不可逆地结合到共聚物中,而四氢呋喃通过活性链末端机理可逆地结合到共聚物中的过程形成远螯共聚物。因此,动力学和热力学因素均可用于控制共聚单体的掺入速率。对导致共聚物形成的竞争反应动力学的研究,通过C-13-NMR对共聚物微观结构的研究以及对环状部分组成的分析,导致了共聚物微观结构与形成的环状部分之间的相关性。因此,说明了环状部分含量对反应条件的依赖性。 [参考:11]

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