Abstract
Anion binding is a timely research field that is developing rapidly because anions play important roles in many areas. Hydrogen (H)-bonding has proven to be a highly effective tool in binding anions due to its directionality and strength. This chapter focuses on the H-bonding-driven anion recognition by neutral receptors that bear H-bond donors, such as (thio)amide, (thio)urea, pyrroles, acidic CHs, and hydroxyl groups. The design and synthesis of receptors based on these binding units have been explored by a number of research groups to achieve a better binding for different kinds of anions in terms of binding constant and selectivity. Recent progress in these aspects is summarized in this chapter. In particular, we emphasize the properties of XH∙∙∙anion (X = N, C, O) H-bonds in the crystal structure of anion complexes, such as the binding mode, the number of H-bonds, and the H-bond lengths and angles. Some solution studies of anion binding including the association constants are also presented. The aim is to provide an overview of this field, including the utilization of H-bonding in anion binding/coordination, the design strategies of the receptors, and their potential applications.
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Cao, L., Zhao, J., Yang, D., Yang, XJ., Wu, B. (2015). Hydrogen Bonding-Driven Anion Recognition. In: Li, ZT., Wu, LZ. (eds) Hydrogen Bonded Supramolecular Structures. Lecture Notes in Chemistry, vol 87. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-45756-6_5
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