1. University of Kragujevac Digital Archive
  2. University of Kragujevac
  3. Faculty of Science, Kragujevac
Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/17352
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dc.rights.licenseAttribution-NonCommercial 3.0 United States*
dc.contributor.authorGutman, Ivan-
dc.contributor.authorFurtula, Boris-
dc.date.accessioned2023-03-17T10:37:46Z-
dc.date.available2023-03-17T10:37:46Z-
dc.date.issued2008-
dc.identifier.citationIvan Gutman & Boris Furtula (2008) CYCLIC CONJUGATION IN PYRACYLENE, Polycyclic Aromatic Compounds, 28:2, 136-142, DOI: 10.1080/10406630801970511en_US
dc.identifier.issn1040-6638en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/17352-
dc.description.abstractCyclic conjugation of the π-electrons in pyracylene is studied by means of the energyeffects (ef) of its various cycles. The calculated ef-values imply that cyclic conjugation significantly destabilizes the pyracylene molecule. This seems to contradict the experimental findings that pyracylene is a reasonably stable conjugated species. We show how this apparent failure of the theory can be avoided, and how the main features of pyracylene’s molecular geometry can be rationalized.en_US
dc.language.isoen_USen_US
dc.publisherTaylor and Francis Publishingen_US
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.sourcePolycyclic Aromatic Compounds-
dc.subjectPyracyleneen_US
dc.subjectcyclic conjugationen_US
dc.subjectenergy effect of cyclic conjugationen_US
dc.subjectmolecular geometryen_US
dc.titleCYCLIC CONJUGATION IN PYRACYLENEen_US
dc.typearticleen_US
dc.description.versionPublisheden_US
dc.identifier.doi10.1080/10406630801970511en_US
dc.type.versionCorrectedVersionen_US
Appears in Collections:Faculty of Science, Kragujevac

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