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Hirshfeld surface analyses and crystal structures of supramolecular self-assembly thiourea derivatives directed by non-covalent interactions

机译:由非共价相互作用引导的超分子自组装硫脲衍生物的Hirshfeld表面分析和晶体结构

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摘要

The novel N-(bis(3,5-dimethoxybenzyl)carbamothioyl)-4-R-benzamide (R: H, Cl, CH3 and OCH3) compounds have been synthesized and characterized by FT-IR, H-1 NMR and C-13 NMR spectroscopy. Their crystal structures were also determined by single-crystal X-ray diffraction studies. Hirshfeld surfaces analysis and their associated two dimensional fingerprint plots of compounds were used as theoretical approach to assess driving force for crystal structure formation via the intermolecular interactions in the crystal lattices of synthesized compounds. The study of X-ray single crystal diffraction and Hirshfeld surfaces analysis of the prepared compounds shows that hydrogen bonding and other weaker interactions such as N-H center dot center dot center dot S, weak C-H center dot center dot center dot S, C-H center dot center dot center dot O, C-H center dot center dot center dot N and C-H center dot center dot center dot pi intermolecular interactions and pi-pi stacking, among molecules of synthesized compounds participate in a cooperative way to stabilize the supramolecular structures. (C) 2017 Elsevier B.V. All rights reserved.
机译:已经合成了新的N-(BIS(3,5-二甲氧基苄基)氨基甲酰基)-4-R-苯甲酰胺(R:H,Cl,CH3和OCH3)化合物,其特征在于FT-IR,H-1 NMR和C- 13 NMR光谱。它们的晶体结构也通过单晶X射线衍射研究确定。 Hirshfeld表面分析及其相关的化合物的相关二维指纹图被用作评估通过合成化合物的晶格中的分子间相互作用来评估晶体结构形成的驱动力的理论方法。制备的化合物的X射线单晶衍射和Hirshfeld表面分析的研究表明,氢键和其他较弱的相互作用如NH中心点中心DOT中心点S,弱CH中心点中心DOT中心DOT S,CH中心DOT中心DOT中心点O,CH中心点中心点中心点N和CH中心点心点中心点PI分子间相互作用和PI-PI堆叠,在合成化合物的分子中参与合作方式以稳定超分子结构。 (c)2017年Elsevier B.V.保留所有权利。

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