Abstract
In this paper, 1H NMR spectroscopy, isothermal titration calorimetry, X-ray crystallography and other characterization methods were used to investigate the interaction modes of tetramethyl cucurbit[6]uril(TMeQ[6]) and three benzimidazole derivatives in an aqueous solution-solid state. The results showed that the aromatic ring moieties in the three derivatives all entered the cavity of TMeQ[6] and their substituents were located at the port of TMeQ[6], forming 1:1 host-guest inclusion complexes. The crystal structures showed that the aromatic part of the benzimidazole derivatives interacted with the cavity of TMeQ[6] via hydrogen bond interactions and the N atoms on the benzimidazole ring formed hydrogen bonds with the carbonyl oxygen of TMeQ[6]. The ion-dipole interactions between [ZnCl4]2− and TMeQ[6] formed supramolecular self-assembly entities.
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This work was supported by the National Natural Science Foundation of China (No.22161010).
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Yang, N., Dai, X., Ma, Y. et al. Study on the Host-Guest Interactions Between Tetramethyl Cucurbit[6]uril and Benzimidazole Derivatives. Chem. Res. Chin. Univ. 39, 1017–1022 (2023). https://doi.org/10.1007/s40242-023-3078-1
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DOI: https://doi.org/10.1007/s40242-023-3078-1