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Preparation and Characterization of Binary Organogels via Some Azobenzene Amino Derivatives and Different Fatty Acids: Self-Assembly and Nanostructures

机译:通过一些偶氮苯氨基衍生物和不同脂肪酸的二元有机凝胶的制备和表征:自组装和纳米结构

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摘要

In present work the gelation behaviors of binary organogels composed of azobenzene amino derivatives and fatty acids with different alkyl chains in various organic solvents were designed and investigated. Their gelation behaviors in 20 solvents were tested as new binary organic gelators. It showed that the length of alkyl substituent chains and azobenzene segment have played a crucial role in the gelation behavior of all gelator mixtures in various organic solvents. Longer alkyl chains in molecular skeletons in present gelators are favorable for the gelation of organic solvents. Morphological studies revealed that the gelator molecules self-assemble into different aggregates from lamella, wrinkle, to belt with change of solvents. Spectral studies indicated that there existed different H-bond formation and hydrophobic force, depending on different substituent chains in molecular skeletons. The present work may also give new perspectives for designing new binary organogelators and soft materials.
机译:在目前的工作中,设计并研究了由偶氮苯氨基衍生物和具有不同烷基链的脂肪酸组成的二元有机凝胶在各种有机溶剂中的凝胶化行为。作为新的二元有机胶凝剂,测试了它们在20种溶剂中的胶凝行为。结果表明,烷基取代基链的长度和偶氮苯链段在各种有机溶剂中的所有胶凝剂混合物的胶凝行为中起着至关重要的作用。在本发明的胶凝剂中,分子骨架中较长的烷基链对于有机溶剂的胶凝是有利的。形态学研究表明,胶凝剂分子自组装成不同的聚集体,从薄片,皱纹到溶剂变化的皮带。光谱研究表明,取决于分子骨架中不同的取代基链,存在不同的氢键形成和疏水力。本工作也可能为设计新型二元有机胶凝剂和软材料提供新的观点。

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