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Título: | Thermochemical insights on the conformational energetics of azepan and azepan-1-ylacetonitrile |
Autor: | Freitas, V.L.S.; Leirosa, S.; Notario, Rafael CSIC ORCID; Ribeiro da Silva, Maria das Dores M. C. | Fecha de publicación: | 2014 | Editor: | American Chemical Society | Citación: | Journal of Organic Chemistry 79: 11583- 11591 (2014) | Resumen: | © 2014 American Chemical Society. This paper is concerned with computational and experimental thermochemical studies of azepan and azepan-1-ylacetonitrile, molecules whose flexible ring structure provides several conformational forms with low energy barriers among them. The computational study describes the energetic analysis of the six most stable conformers on the potential energy surfaces and the determination of their gas-phase standard enthalpy of formation at the reference temperature of 298.15 K. The same gas-phase enthalpic parameters are also derived from the enthalpies of formation in the liquid phase and the enthalpies of vaporization, at T = 298.15 K, determined experimentally using the combustion calorimetry and the Calvet microcalorimetry techniques, respectively. The experimental data reported in this work for the two titled compounds together with other available in the literature for related molecules enabled the establishment of an increments scheme, providing a reliable approach on the prevision of gas-phase enthalpy of formation of cyclic/acyclic hydrocarbons and amines. Complementary, natural bond orbital (NBO) calculations were also performed, allowing an advance on the analysis of the structural and reactivity behavior of these type of compounds. | URI: | http://hdl.handle.net/10261/167889 | DOI: | 10.1021/jo5022376 | Identificadores: | doi: 10.1021/jo5022376 issn: 1520-6904 |
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