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首页> 外文期刊>CrystEngComm >Hydrogen-bonding patterns in a series of multi-component molecular solids formed by 2,3,5,6-tetramethylpyrazine with selected carboxylic acids
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Hydrogen-bonding patterns in a series of multi-component molecular solids formed by 2,3,5,6-tetramethylpyrazine with selected carboxylic acids

机译:由2,3,5,6-四甲基吡嗪与选定的羧酸形成的一系列多组分分子固体中的氢键模式

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The analysis of noncovalent interactions in several complexes constructed from 2,3,5,6-tetramethylpyrazine with different acid ligands, 1,4-cyclohexanedicarboxylic acid, 2,6-dihydroxybenzoic acid, 2,6-pyridinedicarboxylic acid, 6-hydroxy-2-naphthoic acid, 3-nitrophthalic acid, o-phthalic acid and 3-hydroxybenzoic acid, supported by single crystal X-ray diffraction analysis is presented. It reveals that all of these forms except 2 are organic supramolecular cocrystals without charge-transfer between the multicomponent acids and the base. The noncovalent interactions directing the assemblies of the eight structures are managed by classical O-H center dot center dot center dot O, O-H center dot center dot center dot N, weak C-H center dot center dot center dot O and pi-pi stacking interactions to generate 2D or 3D supermolecular architectures. For 5, 6, 7 and 8, carboxyl/pyrazine supramolecular heterosynthons R-2(2)(6) and R-2(2)(8) containing classical O-H center dot center dot center dot N and weak C-H center dot center dot center dot O interactions, usually observed in organic cocrystals of carboxylic acid and heterocyclic base, are again confirmed to participate in constructing these hydrogen-bonding supermolecular networks. In addition, weak C-H center dot center dot center dot O interactions were involved in building and consolidating their structures in all organic complexes. The thermal stability of crystals 1-8 has been investigated by thermogravimetric analysis (TGA) of mass loss.
机译:对由2,3,5,6-四甲基吡嗪与不同酸配体,1,4-环己烷二甲酸,2,6-二羟基苯甲酸,2,6-吡啶二甲酸,6-羟基-2构成的几种配合物中非共价相互作用的分析提出了由单晶X射线衍射分析支持的α-萘甲酸,3-硝基邻苯二甲酸,邻苯二甲酸和3-羟基苯甲酸。它揭示了除2以外的所有这些形式都是有机超分子共晶体,在多组分酸和碱之间没有电荷转移。通过经典OH中心点中心点中心点O,OH中心点中心点中心点N,弱CH中心点中心点中心点O和pi-pi堆积相互作用来管理引导八个结构的装配的非共价相互作用。或3D超分子架构。对于5、6、7和8,包含经典OH中心点中心点中心点N和弱CH中心点中心点的羧基/吡嗪超分子杂合子R-2(2)(6)和R-2(2)(8)中心点O的相互作用(通常在羧酸和杂环碱的有机共晶体中观察到)再次被证实参与构建这些氢键合的超分子网络。此外,在所有有机配合物中,弱的C-H中心点中心点中心点O相互作用都参与了其结构的建立和巩固。晶体1-8的热稳定性已通过质量损失的热重分析(TGA)进行了研究。

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