双(3-羟基-1-甲基吡啶-1-碘化鎓)-18-冠醚-6 超分子共晶体的合成与结构表征

Mageswaran Vijayasri, Natarajan Archana, Chellakarungu Balakrishnan, Mahalingapandian Dhanalakshmi, Shanmugasundaram Parthiban
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引用次数: 0

摘要

以 3-羟基吡啶、碘化甲烷和 18-冠醚-6(18C6)为原料,成功合成了一种新的双(3-羟基-1-甲基吡啶-1-碘化鎓)-18-冠醚-6(I)超分子共晶体。通过傅立叶变换红外光谱(FT-IR)、紫外-可见光谱(UV-DRS)和聚光光谱(PL)、单晶和粉末 X 射线衍射(XRD)分析、扫描电镜和 EDS 分析以及热重分析,对该共晶体进行了表征。粉末 X 射线衍射分析证实了该化合物的体相纯度,而单晶 X 射线衍射分析则证实了该化合物具有中心对称空间群(P21/c)的单斜体系。单晶 XRD 显示其不对称单元为 C6H12O3、[C6H8NO]+[I]¯。C-H⋯O、C-H⋯I 和 O-H⋯I 分子间接触的存在有助于实现晶体内聚。通过漫反射光谱测量,直接带隙能估计为 3.21 eV。热重分析用于确定化合物在温度方面的热行为。EDS 和 SEM 研究用于检测化合物的元素组成和表面形态。
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Synthesis, structural characterization of supramolecular cocrystals of bis(3-hydroxy-1-methylpyridin-1-ium iodide)-18-crown-6
A new supramolecular cocrystal of bis(3-hydroxy-1-methylpyridin-1-ium iodide)-18-crown-6 (I) has been synthesized successfully from 3-hydroxypyridine, methyl iodide and 18-crown-6 (18C6). The cocrystal was characterized by FT-IR, UV-DRS and PL spectroscopy, single crystal and powder X-ray diffraction (XRD) analysis, SEM and EDS analysis, and thermogravimetric analysis. The bulk phase purity of the compound is confirmed by powder XRD analysis, whereas single-crystal XRD confirms that it packs in a monoclinic system with centrosymmetric space group (P21/c). Single crystal XRD shows that the asymmetric unit is C6H12O3, [C6H8NO]+[I]¯. The presence of C–H⋯O, C–H⋯I and O–H⋯I intermolecular contacts helps to achieve crystal cohesion. The direct band gap energy has been estimated to be 3.21 eV using diffuse reflectance spectral measurements. Thermogravimetric analysis was employed to determine the compound’s thermal behaviour concerning temperature. EDS and SEM investigations were used to examine the elemental composition and surface morphology of the compound.
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