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柔性咪唑鎓大环化合物:阴离子诱导自组装的构建单元

Flexible imidazolium macrocycles: building blocks for anion-induced self-assembly.

作者信息

Yang Yu-Dong, Sessler Jonathan L, Gong Han-Yuan

机构信息

College of Chemistry, Beijing Normal University, Xinjiekouwaidajie 19, Beijing, 100875, P. R. China.

出版信息

Chem Commun (Camb). 2017 Aug 29;53(70):9684-9696. doi: 10.1039/c7cc04661h.

Abstract

This feature article summarises recent contributions of the authors in the area of anion-induced supramolecular self-assembly. It is based on the chemistry of a set of tetracationic imidazolium macrocycles, specifically the so-called 'Texas-sized' molecular box, cyclo22 (1), and its congeners, cyclo22 (2), cyclo22 (3), and cyclo22 (4). These systems collectively have been demonstrated as being versatile building blocks that interact with organic carboxylate or sulfonate anions, as well as substrates (e.g., neutral molecules or metal cations). Most work to date has been carried out with 1, a system that has been found to support the construction of a number of stimuli responsive self-assembled ensembles. This macrocycle and others of the 'Texas-sized' box family also show the potential to react as carbene precursors and to undergo post-synthetic modification (PSM) to produce new functional macrocycles, such as trans- and cis-cyclo22 (5 and 6, respectively). On the basis of the work reviewed in this Feature article, we propose that the imidazolium macrocycles 1-4 can be considered as useful tools for the construction of ensembles with environmentally responsive features, including control over self-assembly and an ability to undergo precursor-specific PSM.

摘要

这篇专题文章总结了作者们近期在阴离子诱导的超分子自组装领域所做的贡献。它基于一组四阳离子咪唑鎓大环化合物的化学性质,具体而言是所谓的“德州尺寸”分子盒,即环[2](2,6 - 二(1H - 咪唑 - 1 - 基)吡啶)[2](1,4 - 二亚甲基苯)(1)及其同系物,环[2](2,6 - 二(1H - 咪唑 - 1 - 基)吡啶)[2](1,2 - 二亚甲基苯)(2)、环[2](2,6 - 二(1H - 咪唑 - 1 - 基)吡啶)[2](1,3 - 二亚甲基苯)(3)以及环[2](2,6 - 二(1H - 咪唑 - 1 - 基)吡啶)[2](2,6 - 二亚甲基吡啶)(4)。这些体系已被证明是通用的构建单元,可与有机羧酸根或磺酸根阴离子以及底物(例如中性分子或金属阳离子)相互作用。迄今为止,大多数工作是针对1进行的,该体系已被发现能够支持构建多种刺激响应性自组装聚集体。这种大环化合物以及“德州尺寸”盒家族的其他成员还显示出作为卡宾前体进行反应以及进行后合成修饰(PSM)以产生新的功能大环化合物的潜力,例如反式和顺式环2-N-(2 - ((6 - (1H - 咪唑 - 1 - 基)吡啶 - 2 - 基)氨基)乙烯基)甲酰胺)[2](1,4 - 双甲基苯)(分别为5和6)。基于本专题文章中所综述的工作,我们提出咪唑鎓大环化合物1 - 4可被视为构建具有环境响应特性的聚集体的有用工具,包括对自组装的控制以及进行前体特异性PSM的能力。

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