4,5 -咪唑二羧酸的化学性质及配位势研究进展

W. B. Dirersa
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引用次数: 3

摘要

作为杂环咪唑的一部分,探索新的阴离子受体的兴趣;4,5-咪唑二羧酸及其衍生物在配位化学中具有重要的作用。综述了4,5-咪唑二羧酸(H3IMDC)作为配位化合物潜在基序在超分子结构活性方面的应用和行为。H3IMDC含有一个咪唑NH和两个COOH质子,这些质子可以与阴离子形成氢键。由于羧基氧的电子性质,与金属离子的配位可以以不同的模式发生。原位配体合成作为一种合成配位聚合物的新方法,越来越受到人们的关注。4,5-咪唑二羧酸(H3IMDC)及其衍生物在金属-有机框架配位聚合物中引起关注的主要原因是它具有6个潜在的给体原子:2个咪唑氮原子和4个羧酸氧原子,并能除去1 ~ 3个氢原子,形成H3-nIMDCn- (n=1、2或3)种。六个援助国可以表现出不同的协调方式,构建美丽的结构。本文综述了4,5-咪唑二羧酸的化学性质及其在配位和超分子化学方面的配位潜力,并将其作为药物合成、药理作用和生物活性的输入;综述了咪唑类杂环分子在金属有机骨架中的配位势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review on 4, 5-Imidazoledicarboxylic Acid: Their Chemistry and Coordination Potentials
As part of heterocyclic imidazole interest to explore new receptors for anion; 4,5-imidazoledicarboxylic acid and their derivatives have great roles in coordination chemistry. This review, was also update the application and behaviour of 4,5-imidazoledicarboxylic acid (H3IMDC) as a potential motif for coordination compound in supramolecular structure activity. H3IMDC contains one imidazole NH and two COOH protons which could be donated for hydrogen bonding to the anions. Due to the electronic properties of carboxyl group oxygens, coordination to metal ions can occur in different modes. In situ ligand synthesis is of growing interest as a new approach for the synthesis of coordination polymers. The main reason for interesting of 4,5-imidazoledicarboxylic acid (H3IMDC) and its derivatives in coordination polymers of metal-organic framework is because it has six potential donor atoms: two imidazole nitrogens and four carboxylate oxygen atoms, and can remove one to three hydrogen atoms forming H3-nIMDCn- (n=1,2 or 3) species. The six donors may show various coordination modes and construct beautiful structures. In present review, the chemistry of 4,5-imidazoledicarboxylic acid and its coordination potential in coordination and supramolecular chemistry, which are uses as input for medicinal and drug synthesis, pharmacological actions and as biological activity; where reviewed based on the coordination potentials of imidazole derived heterocyclic molecules in metal-organic frameworks.
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