ArticleChemical communications (Cambridge, England)2019
The road to aryl CHanion binding was paved with good intentions: fundamental studies, host design, and historical perspectives in CH hydrogen bonding.
Article in Chemical communications (Cambridge, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed, 67 citations in OpenAlex.
- Pyridine and N-Pyridinium Functionalized Macrocyclic Squaramide Anion Receptors with High Affinity for Aqueous Sulfate.Chemistry, an Asian journal · 2026Article
- Spectroscopic, X-Ray Crystallographic, and Hirshfeld Surface Analyses for the Investigation of Intermolecular Interactions in Carboxamide Hydrazone Hybrids.ChemistryOpen · 2025Article
- Tunable Anion Recognition at the Lower Rim of Resorcin[4]arenes: Strength, Selectivity, and Transport.JACS Au · 2025Article
- Gem-Diboronic Acids: A Motif for Anion Recognition in Competitive Media.Angewandte Chemie (International ed. in English) · 2025Article
- Tandem catalysis enables chlorine-containing waste as chlorination reagents.Nature chemistry · 2024Article
- Noncovalent Stabilization of Radical Intermediates in the Enantioselective Hydroamination of Alkenes with Sulfonamides.Journal of the American Chemical Society · 2022Article
- Pushing the limits of the hydrogen bond enhanced halogen bond-the case of the C-H hydrogen bond.Chemical science · 2022Article
- Mining anion-aromatic interactions in the Protein Data Bank.Chemical science · 2022Article
- C-H⋯S hydrogen bonding interactions.Chemical Society reviews · 2022Review
- Nonspherical anion sequestration by C-H hydrogen bonding.Chemical science · 2022Article
- Molecular Recognition of Nerve Agents and Their Organophosphorus Surrogates: Toward Supramolecular Scavengers and Catalysts.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021Review
- Carbazole sulfonamide-based macrocyclic receptors capable of selective complexation of fluoride ion.RSC advances · 2021Article
- A neutral porous organic polymer host for the recognition of anionic dyes in water.Chemical science · 2020Article
- Tuning Supramolecular Selectivity for Hydrosulfide: Linear Free Energy Relationships Reveal Preferential C-H Hydrogen Bond Interactions.Journal of the American Chemical Society · 2020Article
- Chiral anion recognition using calix[4]arene-based ureido receptors in aBeilstein journal of organic chemistry · 2020Article
- Hydrogen bond design principles.Wiley interdisciplinary reviews. Computational molecular scienceArticle
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
Throughout the design and development of supramolecular receptors for anion binding, many different non-covalent anion-binding motifs have been employed. One motif seen in many host-guest systems is the sometimes weaker, 'non-traditional' aryl CH hydrogen bond. From June Sutor's discovery of the interaction and its subsequent dismissal by the field in the 1960s to today's use of the aryl CH hydrogen bond in synthetic anion receptors, the path our lab took to begin studying this interaction has been influenced by many other researchers in the field. This feature article highlights the history and properties of the CH hydrogen bond, with a particular focus on aryl CH hydrogen bonds in anion recognition. We highlight select recent developments in the field of anion receptors utilizing aryl CH hydrogen bonds, with an emphasis on how this has influenced the evolution of our approach in designing fundamental studies on CH hydrogen bonding and exploiting this interaction in efforts aimed toward preferential anion binding.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.