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Halogen-Bonding-Driven Self-Assembly of Solvates of Tetrabromoterephthalic Acid

机译:卤素键合驱动的四苯二甲酸溶剂化物的自组装

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摘要

Halogen bonding is one of the most interesting noncovalent attractions capable of self-assembly and recognition processes in both solution and solid phase. In this contribution, we report on the formation of two solvates of tetrabromoterephthalic acid (H2Br4tp) with acetonitrile (MeCN) and methanol (MeOH) viz. H2Br4tp·2MeCN (1MeCN) and H2Br4tp·2MeOH (2MeOH). The host structures of both 1MeCN and 2MeOH are assembled via the occurrence of simultaneous Br···Br, Br···O, and Br···π halogen bonding interactions, existing between the H2Br4tp molecular tectons. Among them, the cooperative effect of the dominant halogen bond in combination with hydrogen bonding interactions gave rise to different supramolecular assemblies, whereas the strength of the halogen bond depends on the type of hydrogen bond between the molecules of H2Br4tp and the solvents. These materials show a reversible release/resorption of solvent molecules accompanied by evident crystallographic phase transitions.
机译:卤素键是能够在溶液和固相中自组装和识别过程的最有趣的非共价景点之一。在这一贡献中,我们报告了用乙腈(MECN)和甲醇(MeOH)viz形成四甲苯二甲酸(H2BR4TP)的两种溶剂化物。 H2BR4TP·2MECN(1MECN)和H2BR4TP·2MEOH(2MEEOH)。在H2BR4TP分子构造之间存在于同时BR····和BR·卤素键合相互作用的同时组装1MECN和2MEOH的主体结构。其中,主导卤素结合与氢键相互作用的合作效应产生了不同的超分子组件,而卤素键的强度取决于H2BR4TP分子与溶剂之间的氢键的类型。这些材料显示可逆释放/再吸收溶剂分子,伴随着明显的晶体相转变。

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