Poly(di-n-pentylsilylene) copolymers containing diethyleneglycol-diethylether side chains

L. A. Schwegler, M. Möller
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引用次数: 5

Abstract

Poly(dipentylsilylene) copolymers containing 4,7,10-trioxadodecylmethylsilylene units as comonomer were synthesized via a Wurtz-type coupling reaction from the corresponding dichlorosilanes. The copolymers were characterized by GPC and NMR spectroscopy. Solvent- and temperature-dependent UV absorption was observed. The bulk polymers underwent broad endothermic transitions below room temperature, whose temperature and heat effect depended on the incorporation of comonomer. This suggested that the high-temperature state can be described as a columnar mesophase corresponding to the well established case of the poly(dipentylsilylene). Correlated to this transition, the copolymers also showed thermochromic behavior at low temperatures. The materials could be oriented by shearing in the mesophase, which was demonstrated by polarized optical microscopy, polarized IR spectroscopy and UV spectroscopy.

含有二乙二醇-二乙醚侧链的聚(二正戊基硅烯)共聚物
以相应的二氯硅烷为共聚单体,通过wurtz型偶联反应合成了以4,7,10-三恶十二基甲基硅烷为共聚单元的聚二戊基硅烯共聚物。用GPC和NMR对共聚物进行了表征。观察到紫外吸收与溶剂和温度有关。整体聚合物在室温下经历了广泛的吸热转变,其温度和热效应取决于共聚单体的掺入。这表明高温态可以被描述为柱状中间相,与聚二戊基硅烯的情况相一致。与这种转变相关,共聚物在低温下也表现出热致变色行为。偏振光显微镜、偏振光红外光谱和紫外光谱分析证实了材料在中间相发生剪切定向。
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