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Synthesis and liquid crystalline properties of a novel series of dimesogenic compounds containing chiral(-) menthyl groups

机译:一系列含有手性(-)薄荷基的成色化合物的合成和液晶性质

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A novel series of symmetric dimesogenic compounds which containing Schiff's base moieties and chiral menthyl groups were designed and synthesized. The target dimesogenic compounds were obtained by the reaction of corresponding (-) menthyl-containing carboxylic acids and 1, 4-bis(aminophenyl-1-oxy)butane, and the outer spacers between Schiff's base moieties and chiral menthyl groups were 2, 4, 6 and 8 methylenes. The chemical structures of this series of dimesogenic compounds and intermediates were characterized by FT-IR, 1H-NMR. The liquid crystalline properties of dimesogenic compounds were characterized by hot-stage coupled polarizing microscopy and DSC. It is found that the liquid crystalline phases much easier to be formed when the outer spacer is longer. When the outer spacer of dimesogenic compound is 8 méthylènes, it can form SmC∗, chiral nematic and an unidentified chiral Sm phases both in heating and cooling process.
机译:设计并合成了一系列新的含席夫碱部分和手性薄荷基的对称二聚化合物。通过相应的含(-)薄荷基的羧酸与1,4-双(氨基苯基-1-氧基)丁烷的反应获得目标二甲生成化合物,席夫碱部分与手性薄荷基之间的外部间隔为2,4 ,6和8个亚甲基。通过FT-IR, 1 H-NMR表征了该系列致二聚化合物和中间体的化学结构。通过热台耦合偏振显微镜和DSC表征了成二成色化合物的液晶性质。发现当外间隔物更长时,液晶相更容易形成。当致二聚化合物的外间隔基为8个甲基时,在加热和冷却过程中均可形成SmC *,手性向列相和未知的手性Sm相。

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