Interlocked host molecules for anion recognition and sensing

被引:126
作者
Caballero, Antonio [1 ]
Zapata, Fabiola [1 ]
Beer, Paul D. [1 ]
机构
[1] Univ Oxford, Chem Res Lab, Dept Chem, Oxford OX1 3TA, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
Anions; Temptation; Interpenetrated structures; Pseudorotaxanes; Rotaxanes; Catenanes; SELF-ASSEMBLED MONOLAYERS; ROTAXANE SYNTHESIS; AQUEOUS-MEDIA; HYDROGEN-BONDS; HALOGEN BONDS; SUPRAMOLECULAR CHEMISTRY; TEMPLATED SYNTHESIS; RECEPTOR MOLECULES; SELECTIVE BINDING; CHLORIDE;
D O I
10.1016/j.ccr.2013.01.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This review describes the concept and exploitation of a strategic anion templation methodology in the construction of a range of interlocked host molecular frameworks designed to recognize anionic guest species in competitive aqueous media. Rotaxane and catenane receptors that contain unique anion binding cavity domains are demonstrated to exhibit high levels of anion selectivity in aqueous media. The incorporation of redox-active ferrocene and photo-active transition metal bipyridyl and naphthalene groups into interlocked host structures enables such materials to selectively sense anions by electro-chemical and optical means. Importantly, halogen bonding interlocked host systems are shown to display enhanced anion recognition properties when compared with hydrogen bonding analogues. The assembly of interlocked architectures capable of displaying anion induced molecular motion, and of increased complexity, such as [3]rotaxanes and a handcuff catenane serves to further illustrate the scope and versatility of this anion templation approach. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:2434 / 2455
页数:22
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