Department of Chemistry and Biochemistry, University of Montana, 32 Campus Drive, Missoula, Montana 59812, United States.
Chem Rev. 2020 Mar 11;120(5):2759-2782. doi: 10.1021/acs.chemrev.9b00583. Epub 2020 Feb 10.
Using anions to induce molecular structure is a rapidly growing area of dynamic and switchable supramolecular chemistry. The emphasis of this review is on helical anion foldamers in solution, and many of the beautiful complexes described herein are accentuated by their crystal structures. Anion foldamers are defined as single- or multistrand complexes-often helical-that incorporate one or more anions. The review begins by discussing foldamer structure and nomenclature and follows with discourse on the anions which are employed. Recent advances in functional foldamers that bind a single anion are examined, including: induced chirality, stimuli-responsive dynamics, fluorescence changes, organocatalysis, anion transport, and halogen bonding. The review then inspects multianion foldamers, and this section is organized by the number of strands within the foldamer-from single- to triple-strand foldamers. Finally, the review is punctuated by recent hydrogen- and halogen-bonding triple-strand anion foldamers.
利用阴离子诱导分子结构是动态和可切换超分子化学中一个快速发展的领域。本篇综述的重点是溶液中的螺旋阴离子折叠体,本文中描述的许多美丽的配合物都通过其晶体结构得到了强调。阴离子折叠体被定义为包含一个或多个阴离子的单链或多链复合物——通常是螺旋状的。综述首先讨论了折叠体的结构和命名法,然后讨论了所使用的阴离子。本文还考察了与单个阴离子结合的功能折叠体的最新进展,包括:诱导手性、刺激响应动力学、荧光变化、有机催化、阴离子传输和卤素键合。然后,综述检查了多阴离子折叠体,本节按照折叠体中的链数进行组织——从单链到三链折叠体。最后,综述以最近的氢键和卤键三链阴离子折叠体为重点。