首页> 外文期刊>Liquid Crystals: An International Journal in the Field of Anisotropic Fluids >Synthesis and liquid crystal properties of a new class of calamitic mesogens based on substituted 2,5-diaryl-1,3,4-thiadiazole derivatives with wide mesomorphic temperature ranges
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Synthesis and liquid crystal properties of a new class of calamitic mesogens based on substituted 2,5-diaryl-1,3,4-thiadiazole derivatives with wide mesomorphic temperature ranges

机译:基于取代的2,5-二芳基-1,3,4-噻二唑衍生物的宽介晶温度范围的新型cal族介晶的合成和液晶性质

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Liquid crystals based on substituted 2,5-diaryl-1,3,4-thiadiazole derivatives (1a-1f, 3a and 3b) and 1,3,4-oxadiazole analogues (2a-2f, 4a and 4b) were synthesised and characterised by 1H, 13C nuclear magnetic resonance, Fourier transform infrared, mass spectrometry, high-resolution mass spectrometry techniques and elemental analyses. The X-ray crystal structure of 1e revealed that it contains tilted lamellar arrangement of molecules in the crystalline solid. The liquid crystal properties have been investigated by polarised-light optical microscopy, differential scanning calorimetry and in-situ variable-temperature X-ray diffraction. All compounds (except 2e and 2f) exhibited thermotropic liquid crystal behaviours with various mesophases (smectic A and C, nematic N or soft crystal E phases). Notably, the 1,3,4-thiadiazole derivatives consistently have wider mesomorphic temperature ranges than those of the respective 1,3,4-oxadiazole analogues. The solutions of all compounds in CH2Cl2 individually displayed one or two absorption bands with max values at 297-355nm and emitted with max values at 363-545nm and quantum yields of 0.12-0.73. Structure-property relationships of these compounds are discussed in the contexts of their molecular structures and weak intermolecular interactions.
机译:合成并表征了基于取代的2,5-二芳基-1,3,4-噻二唑衍生物(1a-1f,3a和3b)和1,3,4-恶二唑类似物(2a-2f,4a和4b)的液晶通过1H,13C核磁共振,傅里叶变换红外光谱,质谱,高分辨率质谱技术和元素分析。 1e的X射线晶体结构表明,它在结晶固体中包含倾斜的分子层状排列。通过偏光光学显微镜,差示扫描量热法和原位可变温度X射线衍射研究了液晶性质。所有化合物(2e和2f除外)均表现出具有各种中间相(近晶A和C,向列N或软晶E相)的热致液晶行为。值得注意的是,1,3,4-噻二唑衍生物始终比各自的1,3,4-恶二唑类似物具有更宽的介晶温度范围。 CH2Cl2中所有化合物的溶液分别显示一个或两个吸收带,最大值在297-355nm处,发射出的最大值在363-545nm处,且量子产率为0.12-0.73。在它们的分子结构和弱分子间相互作用的背景下讨论了这些化合物的结构-性质关系。

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