Abstract
The structure of water–acetonitrile solutions of derivatives of quinoline and tetrahydroquinoline is investigated by means of аb initio molecular dynamics. It is shown that the propensity of molecules to form different types of hydrogen bonds depends largely on both the nature of the functional groups and on steric factors. When porous graphitic carbon is used as a sorbent, a linear correlation is observed between the fraction of configurations with hydrogen bonds and the logarithm of the retention factor under conditions of reverse-phase liquid chromatography.
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ACKNOWLEDGMENTS
This work was supported by the RF Ministry of Education and Science, project no. 4.5883.2017/BCh; and by megagrant no. 14.V25.31.0005.
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Translated by L. Brovko
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Nekrasova, N.A., Kurbatova, S.V. Intermolecular Interactions in Water–Acetonitrile Solutions of Quinoline. Russ. J. Phys. Chem. 93, 67–74 (2019). https://doi.org/10.1134/S0036024418120324
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DOI: https://doi.org/10.1134/S0036024418120324