Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding

Abstract

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.

Graphical abstract: Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding

Supplementary files

Article information

Article type
Communication
Submitted
31 Mar 2024
Accepted
11 May 2024
First published
13 May 2024

Chem. Commun., 2024, Advance Article

Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding

C. Liu, C. Zhang, Z. Li, J. Chen, T. Wang, X. Zhang, M. Yan and B. Zhai, Chem. Commun., 2024, Advance Article , DOI: 10.1039/D4CC01472C

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