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支柱芳烃:具有光明未来的迷人环芳烃。

Pillar[5]arenes: fascinating cyclophanes with a bright future.

机构信息

School of Pharmacy and Biomolecular Sciences, Huxley Building, University of Brighton, Brighton BN2 4GJ, UK.

出版信息

Chem Soc Rev. 2012 Jan 21;41(2):597-607. doi: 10.1039/c1cs15164a. Epub 2011 Jul 29.

Abstract

Pillar[5]arenes are [1(5)]paracyclophane derivatives consisting of 1,4-disubstituted hydroquinones linked by methylene bridges in the 2,5-positions. The first report of these novel macrocycles was in 2008, when 1,4-dimethoxypillar[5]arene was prepared in 22% yield, and subsequent improvements in synthetic methods have allowed the number of derivatives to expand significantly. In addition to D(5) symmetric pillar[5]arenes, asymmetric pillar[5]arenes with two different substituents in the 1- and 4-positions and copillar[5]arenes consisting of two different repeat units in a 4 : 1 ratio have been synthesised. Crystallographic, computational and spectroscopic studies are starting to shed light on the compounds' unusual inclusion phenomena, from gelation and transportation of water through nanotubes to the formation of chromogenic rotaxanes. Applications as molecular sensors are starting to appear with a focus on guest detection by fluorescence quenching. This tutorial review will provide a summary of research into the pillar[5]arenes since their recent discovery.

摘要

支柱芳烃是[1(5)]对环芳烷的衍生物,由 2,5-位通过亚甲基桥连接的 1,4-二取代对苯二酚组成。这些新型大环的首次报道是在 2008 年,当时以 22%的收率制备了 1,4-二甲氧基支柱[5]芳烃,随后对合成方法的改进显著扩大了衍生物的数量。除了 D(5)对称的支柱[5]芳烃外,还合成了在 1-和 4-位具有两个不同取代基的不对称支柱[5]芳烃和由 4:1 比例的两个不同重复单元组成的共支柱[5]芳烃。晶体学、计算和光谱研究开始揭示这些化合物不寻常的包容现象,从通过纳米管凝胶化和输送水到形成显色轮烷。作为分子传感器的应用开始出现,重点是通过荧光猝灭检测客体。本综述将提供自最近发现以来对支柱[5]芳烃的研究总结。

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