Synthesis of liquid crystalline epoxy monomers

J. Fabia, H. Galina, B. Mossety-Leszczak, J. Ulański, P. Wojciechowski, A. Włochowicz
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引用次数: 2

Abstract

A two-stage method of synthesis of liquid-crystalline diepoxy monomers has been developed. In the first stage, esterification of 4-hydroxyphenyl-4-hydroxybenzoate or 4,4'- biphenol or 4,4'-dihydroxyazobenzene was carried out using 4-penetenoic acid. The resulting olefinic precursors were oxidized with m-chloroperoxybenzoic acid to introduce the epoxy groups. The structure of products was confirmed by FT- IR and 1H NMR. Examinations on a polarization microscope with a hot plate confirmed the presence of mesomorphic phases in both the precursors and monomers. The phase transition temperatures were in the range of 73.5 (at cooling) to 128.0 degree(s)C for olefinic precursors and in the range 57.1 (at cooling) to 143 degree(s)C for epoxy compounds, as determined by DSC and thermo-optical analysis (TOA).
液晶环氧单体的合成
提出了一种两步法合成液晶二氧基单体的方法。第一阶段,用4-戊烯酸酯化4-羟基苯甲酸酯或4,4'-双酚或4,4'-二羟基偶氮苯。合成的烯烃前驱体与间氯过氧苯甲酸氧化生成环氧基。产物的结构经FT- IR和1H NMR确证。用热板偏光显微镜检查证实了前体和单体中均存在中晶相。通过DSC和热光学分析(TOA)测定,烯烃前驱体的相变温度范围为73.5(冷却)~ 128.0℃,环氧化合物的相变温度范围为57.1(冷却)~ 143℃。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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