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Hydrogen bonding vs. halogen bonding: the solvent decides

机译:氢键与卤素键:溶剂决定

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摘要

Control of intermolecular interactions is integral to harnessing self-assembly in nature. Here we demonstrate that control of the competition between hydrogen bonds and halogen bonds, the two most highly studied directional intermolecular interactions, can be exerted by choice of solvent (polarity) to direct the self-assembly of co-crystals. Competitive co-crystal formation has been investigated for three pairs of hydrogen bond and halogen bond donors, which can compete for a common acceptor group. These competitions have been examined in seven different solvents. Product formation has been determined and phase purity has been examined by analysis of powder X-ray diffraction patterns. Formation of hydrogen-bonded co-crystals is favoured from less polar solvents and halogen-bonded co-crystals from more polar solvents. The solvent polarity at which the crystal formation switches from hydrogen-bond to halogen-bond dominance depends on the relative strengths of the interactions, but is not a function of the solution-phase interactions alone. The results clearly establish that an appreciation of solvent effects is critical to obtain control of the intermolecular interactions.
机译:分子间相互作用的控制对于自然地利用自组装是必不可少的。在这里我们证明控制氢键和卤素键之间的竞争是两个研究最深入的方向分子间相互作用,可以通过选择溶剂(极性)来控制共晶体的自组装。已经研究了三对氢键和卤素键供体的竞争共晶形成,它们可以竞争一个共同的受体基团。这些竞争已在七种不同的溶剂中进行了研究。通过粉末X射线衍射图的分析,已经确定了产物的形成并且已经检查了相纯度。极性较小的溶剂有利于氢键合晶体的形成,极性较大的溶剂有利于卤素键合晶体的形成。晶体形成从氢键主导转变为卤素键优势的溶剂极性取决于相互作用的相对强度,但不是溶液相相互作用的函数。结果清楚地表明,对溶剂作用的认识对于获得分子间相互作用的控制至关重要。

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