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Интеллектуальная Система Тематического Исследования НАукометрических данных |
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Structural Descriptors of Benzenoid Hydrocarbons: A Mismatch between the Estimates and Parity Effects in Helicenesстатья
- Авторы: Sabirov Denis Sh, Ori Ottorino, Tukhbatullina Alina A., Shepelevich Igor S.
- Журнал: C — Journal of Carbon Research
- Том: 8
- Номер: 3
- Год издания: 2022
- Издательство: MDPI
- Местоположение издательства: Basel, Switzerland
- Номер статьи: 42
- DOI: 10.3390/c8030042
- Аннотация: Benzenoid hydrocarbons have regular structures, attracting the opportunity to test the structural descriptors of their series. In the present study, we compared information entropy, Wiener indices, topological efficiencies, topological roundness, and symmetries of oligoacenes, phenacenes, and helicenes. We found and discussed the mismatches between the descriptors and the symmetry of benzenoids. Among the studied series, helicenes demonstrate the parity effect when the information entropy and topological roundness form saw-like functions depending on the number of the member, odd or even. According to our quantum chemical calculations, this parity effect has no consequences for such molecular properties as molecular polarizability and frontier molecular orbital energies. Further, we demonstrated that the changes in the structural descriptors upon the chemical reactions of benzenoids could be used for the numerical description of chemical processes. Interestingly, the view of the information entropy reaction profile is similar to the energy profiles of chemical reactions. Herewith, the intermediate chemical compounds have higher information entropy values compared with the initial and final compounds, which reminisce the activation barrier.
- Добавил в систему: Сабиров Денис Шамилевич