Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9228
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dc.rights.licenseBY-NC-ND-
dc.contributor.authorRadenkovic, Slavko-
dc.contributor.authorTošović, Jelena-
dc.contributor.authorHavenith R.-
dc.contributor.authorBultinck P.-
dc.date.accessioned2020-09-19T17:47:45Z-
dc.date.available2020-09-19T17:47:45Z-
dc.date.issued2015-
dc.identifier.issn1439-4235-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9228-
dc.description.abstract©2015 Wiley-VCH Verlag GmbH & Co. KGaA , Weinheim. The effect of benzo and benzocyclobutadieno annelation on the current density induced in a series of biphenylene derivatives is examined at the B3LYP/cc-pVDZ level of theory, by using the CTOCD-DZ method. Angular benzo annelation increases, whereas linear benzo annelation decreases the intensity of paratropic (antiaromatic) current density along the fourmembered ring of biphenylene. The opposite effect is found for benzocyclobutadieno annelation. It is shown that the extent of local aromaticity of the four-membered ring in biphenylene congeners can vary from highly antiaromatic to nonaromatic, as a result of different modes of annelation.-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceChemPhysChem-
dc.titleRing currents in benzo- And benzocyclobutadieno-annelated biphenylene derivatives-
dc.typearticle-
dc.identifier.doi10.1002/cphc.201402468-
dc.identifier.scopus2-s2.0-84920175280-
Appears in Collections:Faculty of Science, Kragujevac

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