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首页> 外文期刊>Macromolecules >Influences of hydrogen bonding and peripheral chain length on mesophase structures of mesogen-jacketed liquid crystalline polymers with amide side-chain linkages
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Influences of hydrogen bonding and peripheral chain length on mesophase structures of mesogen-jacketed liquid crystalline polymers with amide side-chain linkages

机译:氢键和外围链长对带有酰胺侧链键的介晶夹层液晶聚合物中间相结构的影响

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摘要

A series of mesogen-jacketed liquid crystalline polymers, poly{2,5-bis[(4-alkoxyphenyl)aminocarbonyl]styrene} (P-Cm, where m is the number of carbon atoms in the alkoxy groups, and m = 1, 4, 8, 12), with an amide core and flexible tails of varying lengths on the two ends in the side chain were designed and successfully synthesized via conventional radical polymerization. The mesophase structures of these polymers were dependent on the number of carbon atoms in the peripheral chains. Wide-angle X-ray diffraction and polarized light microscopy results revealed that the polymers with m ≥ 4 could form smectic A phases, while a columnar nematic phase could be formed for the polymer with methoxy end groups (P-C1). The hydrogen bonding among the side-chain amide groups might play an important role in forming and stabilizing these liquid crystalline phases, which was suggested by the results from variable-temperature FTIR and 2D IR analyses.
机译:一系列介晶包覆的液晶聚合物,聚{2,5-双[(4-烷氧基苯基)氨基羰基]苯乙烯}(P-Cm,其中m是烷氧基中的碳原子数,m = 1,在图4、8、12)中,设计了酰胺核并在侧链的两端具有可变长度的柔性尾,并通过常规自由基聚合成功地合成了该尾。这些聚合物的中间相结构取决于外围链中的碳原子数。 X射线广角衍射和偏光显微镜观察结果表明,m≥4的聚合物可形成近晶A相,而甲氧基端基(P-C1)则可形成柱状向列相。可变温度FTIR和2D IR分析的结果表明,侧链酰胺基之间的氢键可能在形成和稳定这些液晶相中起重要作用。

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