Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding
In this study, a benzoselenadiazole- and pyridine-bifunctionalized hydrogen-bonded arylamide foldamer was synthesized. A co-crystallization experiment with 1,4-diiodotetrafluorobenzene showed that a new type of supramolecular double helices, which were induced by three orthogonal interactions, namel...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-06, Vol.6 (47), p.663-666 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study, a benzoselenadiazole- and pyridine-bifunctionalized hydrogen-bonded arylamide foldamer was synthesized. A co-crystallization experiment with 1,4-diiodotetrafluorobenzene showed that a new type of supramolecular double helices, which were induced by three orthogonal interactions, namely, three-center hydrogen bonding (O H O), I N halogen bonding and Se N chalcogen bonding, have been constructed in the solid state. This work presents a novel instance of multiple non-covalent interactions that work together to construct supramolecular architectures.
A new type of supramolecular helix induced by three types of orthogonal interaction, hydrogen bonding (O H O), halogen bonding (I N and I F) and chalcogen bonding (Se N), was constructed. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d4cc01472c |