Patrick Sophie C, Beer Paul D, Davis Jason J
Department of Chemistry, University of Oxford, Oxford, UK.
Nat Rev Chem. 2024 Apr;8(4):256-276. doi: 10.1038/s41570-024-00584-4. Epub 2024 Mar 6.
Anion recognition is pertinent to a range of environmental, medicinal and industrial applications. Recent progress in the field has relied on advances in synthetic host design to afford a broad range of potent recognition motifs and novel supramolecular structures capable of effective binding both in solution and at derived molecular films. However, performance in aqueous media remains a critical challenge. Understanding the effects of bulk and local solvent on anion recognition by host scaffolds is imperative if effective and selective detection in real-world media is to be viable. This Review seeks to provide a framework within which these effects can be considered both experimentally and theoretically. We highlight proposed models for solvation effects on anion binding and discuss approaches to retain strong anion binding in highly competitive (polar) solvents. The synthetic design principles for exploiting the aforementioned solvent effects are explored.
阴离子识别与一系列环境、医药和工业应用相关。该领域的最新进展依赖于合成主体设计的进步,以提供广泛的有效识别基序和新型超分子结构,这些结构能够在溶液中和衍生的分子膜中实现有效结合。然而,在水性介质中的性能仍然是一个关键挑战。如果要在实际介质中实现有效和选择性检测,了解本体和局部溶剂对主体支架阴离子识别的影响至关重要。本综述旨在提供一个框架,在其中可以从实验和理论两方面考虑这些影响。我们重点介绍了关于溶剂化对阴离子结合影响的模型,并讨论了在高竞争性(极性)溶剂中保持强阴离子结合的方法。探索了利用上述溶剂效应的合成设计原则。