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Synthesis and mesomorphic property of 2,5-aryl-1,3,4-oxadiazole/thiadiazole derivatives bearing a terminal thiophene unit

机译:含有末端噻吩单元的2,5-芳基-1,3,4-恶二唑/噻二唑衍生物的合成及其同形性质

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The synthesis and characterization of a series of heterocyclic compounds 2a-2d based on 1,3,4-oxadiazole/ thiadiazole, furan and thiophene units are reported. The thermal behaviors of these compounds were investigated by means of differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and thermogravimetric analysis (TGA). The 1,3,4-thiadiazole derivative 2b exhibited enantiotropic smectic C and A mesophases with wide temperature range and good thermal stability, while all of the other compounds did not show liquid crystalline behaviors. The results indicate that 1,3,4-thiadiazole-based compounds are more beneficial to form stable mesophases than the corresponding 1,3,4-oxadiazole analogues, and the compounds with a central furan unit as the rigid core may result in the loss of the meosgenic behaviors due to the non-linear molecular structure.
机译:报道了基于1,3,4-二唑/噻二唑,呋喃和噻吩单元的一系列杂环化合物2a-2d的合成与表征。通过差示扫描量热法(DSC),偏振光学显微镜(POM)和热重分析(TGA)来研究这些化合物的热行为。 1,3,4-噻二唑衍生物2b表现出脱嗜脱色的偏晶c和具有宽温度范围和良好热稳定性的中间蛋白酶,而所有其他化合物都没有显示出液晶行为。结果表明,基于1,3,4-噻二唑类化合物比相应的1,3,4-二唑类似物形成稳定的中间蛋白酶,以及与刚性芯的中央呋喃单元的化合物可能导致损失非线性分子结构引起的梅多斯必要行为。

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