Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/17366
Title: Cyclic conjugation in mono- and dicyclopenta-derivatives of anthracene and phenanthrene
Authors: Gutman, Ivan
Đurđević Nikolić, Jelena
Furtula, Boris
Milivojević, Bojana
Journal: Indian Journal of Chemistry A
Issue Date: 2008
Abstract: The energy effects of cycles and pairs of cycles in mono- and dicyclopenta-derivatives of anthracene and phenanthrene tire 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]antracene (stable) <dicyclopenta[jk,mn]phenanthrene (stable even at >1000 degrees C).
URI: https://scidar.kg.ac.rs/handle/123456789/17366
Type: article
ISSN: 0376-4710
Appears in Collections:Faculty of Science, Kragujevac

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