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Назив: Dependence of the Enthalpy of Formation of Phenols on Molecular Structure–Semiempirical Study
Аутори: Markovic, Svetlana
Redžepović, Izudin
Furtula, Boris
Датум издавања: 2019
Сажетак: © 2019, © 2019 Taylor & Francis Group, LLC. The ability of three semiempirical methods (PM3, PM5, and PM7) in reproducing the enthalpy of formation (ΔfH°) of polycyclic aromatic phenols (PAPs) was tested by comparing experimental and calculated values for 33 compounds. In addition, the results from the semiempirical methods were compared to those obtained from the suitable isodesmic reactions, performed using the B3LYP–D3 and M06–2X functionals in combination with the 6-311 + G(d,p) basis set. With an average absolute error less than 10 kJ mol−1, all five methodologies yielded mutually comparable results. Considering low computational cost of semiempirical methods, the influence of structural features on ΔfH° of PAPs was investigated using the PM5 and PM7 methods. It was found that the greatest influence on ΔfH° has the size of the molecules, while the effects of other properties, i.e., the position of the OH group, number of bay regions, and molecular branching are weaker. The influence of the OH group position decreases with its moving away from molecular ends, and eventually becomes insignificant. As branching and the number of bay regions are mutually dependent and respective molecules are often nonplanar, it is difficult to examine individual contributions of these two structural features. In general, ΔfH° decreases with increasing number of bay regions and molecular branching.
URI: https://scidar.kg.ac.rs/handle/123456789/10962
Тип: article
DOI: 10.1080/10406638.2019.1696379
ISSN: 1040-6638
SCOPUS: 2-s2.0-85076057766
Налази се у колекцијама:Faculty of Science, Kragujevac

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