Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/2103
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dc.contributor.authorGutman, Ivan-
dc.contributor.authorĐurđević, Jelena-
dc.contributor.authorFurtula, Boris-
dc.contributor.authorMilivojević, Bojana-
dc.date.accessioned2008-09-25T10:55:53Z-
dc.date.available2008-09-25T10:55:53Z-
dc.date.issued2008-06-
dc.identifier.issn0376-4710-
dc.identifier.urihttp://hdl.handle.net/123456789/2103-
dc.description803-807en_US
dc.description.abstractThe energy effects of cycles and pairs of cycles in mono- and dicyclopenta-derivatives of anthracene and phenanthrene are computed by a graph-theoretical method. Our results show that there is no significant difference between the extent of cyclic conjugation in anthracene and its cyclopenta-derivative (aceanthrylene) and phenanthrene and its cyclopenta-derivative (acephenanthrylene). In contrast to this, the presence of two cyclopentane rings causes drastic changes in the modes of cyclic conjugation. Our results provide an explanation for the peculiar stability order: dicyclopenta[de,mn] anthracene (never isolated) < dicyclopenta[de,kl]anthracene (stable) 1000oC).en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCA Vol.47A(6) [June 2008]en_US
dc.titleCyclic conjugation in mono- and dicyclopenta-derivatives of anthracene and phenanthreneen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.47A(06) [June 2008]

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