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Substituted Aroylhydrazone Based Polycatenars: Tuning of Liquid Crystalline Self-Assembly

机译:取代的基于阿罗伊氢唑的聚载体:液晶自组装的调整

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A systematic investigation on mesomorphic properties of two new classes of substituted-aroylhydrazones having semi-flexible ester (ester based polycatenars) and flexible ether linker (ether based polycatenars) with variable alkoxy chain length (n=6, 8, 10, 12, 14, 16) are described. The members of each series with six soft alkoxy chains formed columnar self-assembly as confirmed by differential scanning calorimetry analysis, polarized optical microscopy and powder X-ray diffraction studies. For the ester based polycatenar scaffolds, the mesophase of lower alkoxy chain members exhibited columnar oblique phase which further transformed to columnar hexagonal phase with the increase in the chain length and thus showing a mesophase crossover phenomenon. In the case of ether based polycatenars, the presence of ether link provides significant stabilization of the columnar oblique phase for all the members except the lower homologues. The driving forces for the appearance of columnar self-assembly are the intermolecular hydrogen-bonding interactions between the amide groups (-C=O···H-N-) of aroylhydrazone core, which was confirmed by the temperature dependent IR studies. In addition, both the series of compounds exhibit good gelation properties, which is assisted by the intermolecular hydrogen bonding.
机译:对具有半灵性酯(基于酯的聚猫酯)和柔性醚链接(基于乙醚的聚猫烯)的两种新型替代的 - 芳烃的介导特性的系统研究,16)被描述。通过差异扫描量热法分析,极化光学显微镜和粉末X射线衍射研究证实,每个系列的成员都具有六个软烷基链形成柱状自组装。对于基于酯的多猫支架,下烷氧基链成员的中间体表现出柱状斜相,该相进一步转化为柱状六边形相,随着链长的增加,从而显示了中间体的交叉现象。在基于乙醚的多猫的情况下,除较低同源物以外,所有成员的圆柱斜相的存在可显着稳定。出现柱状自组装的驱动力是Aroylhydrazone核心的酰胺组(-c = O··H-N-)之间的分子间氢键相互作用,这是由温度依赖性IR研究证实的。此外,这两种化合物都表现出良好的凝胶化性能,并在分子间氢键的帮助下。

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