Abstract
Dependences of sorption energies of sulfur-, oxygen-, and nitrogen-containing heterocyclic compounds on the nature of heteroatoms, structure of substituents and their position in the ring were studied. The contributions of heteroatoms, functional and alkyl groups to the energy of dispersive interaction of position isomers with nonpolar stationary phases were determined for imidazoles, piperidines, morpholines, thiomorpholines, dioxalanes, oxathiolanes, dithiolanes, thiophenes, and furans. The nonequivalence of contributions of the same substituents to the sorption energy of each of the heterocyclic compounds, depending on the nature of the heteroatom and position of the substituent, was shown. The obtained values of contributions of heteroatoms and substituents can be used for apriori calculation of retention indices of position isomers of five- and six-membered heterocycles containing one or two heteroatoms in the ring.
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Translated from lzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 2033–2038, August, 1996.
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Golovnya, R.V., Misharina, T.A. Thermodynamic characteristics of sorption of heterocyclic compounds m capillary gas chromatography. Russ Chem Bull 45, 1928–1933 (1996). https://doi.org/10.1007/BF01457779
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DOI: https://doi.org/10.1007/BF01457779