Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10162
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dc.rights.licenserestrictedAccess-
dc.contributor.authorGutman I.-
dc.contributor.authorMarkovic, Svetlana-
dc.contributor.authorJeremic B.-
dc.date.accessioned2021-04-20T15:02:24Z-
dc.date.available2021-04-20T15:02:24Z-
dc.date.issued2010-
dc.identifier.issn1040-6638-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10162-
dc.description.abstractFor a long time, Kekulé structures have been used to predict and rationalize the stability, geometry, and π-electron properties of polycyclic conjugated molecules, especially hydrocarbons. We now point out an example, demonstrating that the Kekulé-structure model is not generally applicable. Namely, the molecule of dibenzo[cd,mn]indeno[123, gf ]pyrene is perfectly planar and strain-free. Yet, its geometry (determined by means of an unrestricted symmetry-broken UB3LYP/6-311G(d,p) DFT method) is in complete disagreement with what one would expect on the basis of its Kekulé structures. © Taylor & Francis Group, LLC.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourcePolycyclic Aromatic Compounds-
dc.titleA case of breakdown of the Kekulé-structure model-
dc.typearticle-
dc.identifier.doi10.1080/10406638.2010.503162-
dc.identifier.scopus2-s2.0-77956622983-
Appears in Collections:Faculty of Science, Kragujevac

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