Helical Anion Foldamers in Solution

Eric A. John, Casey J. Massena, Orion B. Berryman

Research output: Contribution to journalArticlepeer-review

82 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)2759-2782
Number of pages24
JournalChemical Reviews
Volume120
Issue number5
DOIs
StatePublished - Mar 11 2020

Funding

We are thankful for funding provided by the National Science Foundation (NSF) CAREER CHE-1555324, the Center for Biomolecular Structure and Dynamics CoBRE (NIH NIGMS grant P20GM103546), and the University of Montana (UM). We give a special thanks to Dan Decato for his continued feedback. We thank Professor Kyu-Sung Jeong and Professor Máté Erdélyi for helpful conversations.

Funder number
CHE-1555324
P20GM103546

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