Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10175
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dc.contributor.authorJeremić O.-
dc.contributor.authorRadenkovic, Slavko-
dc.contributor.authorGutman I.-
dc.date.accessioned2021-04-20T15:04:34Z-
dc.date.available2021-04-20T15:04:34Z-
dc.date.issued2010-
dc.identifier.issn0352-5139-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10175-
dc.description.abstractCyclic conjugation in benzo-annelated triphenylenes was studied by means of the energy effect (ef) and the p-electron content (EC) of the six- -membered rings. A regularity that was earlier discovered in the case of acenaphthylene and fluoranthene congeners is now shown to hold also for benzo-annelated triphenylenes: Benzenoid rings that are annelated angularly with regard to the central six-membered ring Z0 of triphenylene increase the intensity of the cyclic conjugation in Z0, whereas linearly annelated benzenoid rings decrease the cyclic conjugation in Z0. The ef- and EC-values are strongly correlated, yet in a non-linear manner.-
dc.rightsrestrictedAccess-
dc.sourceJournal of the Serbian Chemical Society-
dc.titleCyclic conjugation in benzo-annelated triphenylenes-
dc.typearticle-
dc.identifier.doi10.2298/JSC091201068J-
dc.identifier.scopus2-s2.0-77955765224-
Appears in Collections:Faculty of Science, Kragujevac

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