Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10457
Title: Anomalous cyclic conjugation in the perylene/bisanthrene homologous series
Authors: Gutman I.
Đurđević Nikolić, Jelena
Radenkovic, Slavko
Matović, Zoran
Journal: Monatshefte fur Chemie
Issue Date: 1-Dec-2012
Abstract: The homologous series of benzenoid hydrocarbons, whose first members are perylene (P1), bisanthrene (P2), and tetrabenzo[bc,ef,kl,no]coronene (P3), are usually considered as consisting of to two polyacene fragments, joined by essentially single carbon-carbon bonds, forming empty rings, devoid of any cyclic conjugation. In higher members of this series, the pattern of cyclic conjugation is found to be significantly different from that predicted by means of Kekulé-structure-based models. Various measures of local aromaticity (NICS, HOMA, SCI), calculated at the B3LYP/6-311 ? G(d,p) level of DFT theory, all indicate that cyclic conjugation in the empty rings in the middle of the molecule has a high value, exceeding those in the rings of the polyacene fragments. This anomaly begins at P 4 and was demonstrated to exist at least until P 7. © Springer-Verlag 2012.
URI: https://scidar.kg.ac.rs/handle/123456789/10457
Type: article
DOI: 10.1007/s00706-012-0840-3
ISSN: 00269247
SCOPUS: 84870324731
Appears in Collections:Faculty of Science, Kragujevac

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