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首页> 外文期刊>Crystal growth & design >Cobalt complexes appended with para - And meta -arylcarboxylic acids: Influence of cation, solvent, and symmetry on hydrogen-bonded assemblies
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Cobalt complexes appended with para - And meta -arylcarboxylic acids: Influence of cation, solvent, and symmetry on hydrogen-bonded assemblies

机译:带有对-和间-芳基羧酸的钴配合物:阳离子,溶剂和对称性对氢键组装体的影响

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摘要

The present work shows the syntheses, structures, and hydrogen-bonding- based self-assembly of Co~(3+) coordination complexes containing appended arylcarboxylic acid groups. The carboxylic acid groups are present at either the para or the meta position of the appended arene ring. Every Co ~(3+) coordination complex offers both hydrogen-bond donors (in O-H groups of arylcarboxylic acid) and acceptors (in C=O_(amide) groups as well as C=O_(acid) of arylcarboxylic acid) in a single molecule. As a consequence, all molecules self-assemble in a highly complementary and unique structural fashion via an array of inter- and intramolecular hydrogen bonding. The position of carboxylic acid, presence of cation, type of cation, and solvent of crystallization has significantly affected/altered the self-assembly process of complementary functional groups.
机译:本工作显示了含有附加的芳基羧酸基团的Co〜(3+)配位配合物的合成,结构和基于氢键的自组装。羧酸基团存在于所连接的芳烃环的对位或间位。每个Co〜(3+)配位化合物都可在单个氢键上同时提供氢键供体(在芳基羧酸的OH基中)和受体(在C = O_(酰胺)基以及C = O_(酸)中)分子。结果,所有分子通过一系列分子间和分子内氢键以高度互补和独特的结构方式自组装。羧酸的位置,阳离子的存在,阳离子的类型和结晶溶剂已显着影响/改变了互补官能团的自组装过程。

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