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首页> 外文期刊>Macromolecules >Preparation of telechelic polysilylenes: A general methodology for the synthesis of polysilylene-based triblock copolymers
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Preparation of telechelic polysilylenes: A general methodology for the synthesis of polysilylene-based triblock copolymers

机译:远螯聚硅氧烷的制备:合成基于聚硅氧烷的三嵌段共聚物的通用方法

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摘要

Telechelic polysilylenes have been developed involving the chemical degradation of poly-(di-n-hexylsilylene) with bromine. The molecular weight of the newly formed telechelic PDHS depends on the ratio of bromine to the starting PDHS. The percentage of end groups increases as the molecular weight of the telechelic PDHS is lowered, reaching a maximum of 99% difunctionality. Polystyrene-PDHS-polystyrene triblock copolymers have been prepared by coupling polystyryllithium to the telechelic PDHS in the presence of cryptand [2.1.1]. The effect of molecular weight on the disordering transition of PDHS into a columnar mesophase has been studied, and temperature and enthalpy have been shown to decrease by the presence of the PS end groups and eventually became unobservable at high fractions of PS. The morphologies of the triblock copolymers were studied by atomic force microscopy.
机译:已经开发出远螯聚硅氧烷,涉及用溴化学降解聚(二正己基甲硅烷基)。新形成的远螯PDHS的分子量取决于溴与起始PDHS的比例。端基的百分比随着远螯PDHS分子量的降低而增加,最大达到99%的双官能度。聚苯乙烯-PDHS-聚苯乙烯三嵌段共聚物是通过在有穴状配体[2.1.1]的情况下将聚苯乙烯锂与远螯PDHS偶联而制备的。已经研究了分子量对PDHS无序转变为柱状中间相的影响,并且由于PS端基的存在,温度和焓已显示降低,最终在高比例的PS下变得不可观察。通过原子力显微镜研究了三嵌段共聚物的形态。

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