Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10187
Title: Hydrogen-mediated Stone-Wales isomerization of dicyclopenta[de,mn] anthracene
Authors: Stanković, Vladimir
Markovic, Svetlana
Gutman I.
Sretenovic Z.
Issue Date: 2010
Abstract: The mechanism of transformation of two radicals (R1p and R1i) obtained by addition of a hydrogen atom to an external and internal carbon atom of dicyclopenta[de,mn]anthracene (P1) was investigated. Two pathways were revealed. The first mechanism is a one-step process, whereas the second mechanism includes two transition states and a cyclobutyl intermediate. The formation of R1p and R1i and the homolytic cleavage of the radicals obtained during the isomerization processes were also examined. In both pathways the addition of a hydrogen atom to the internal carbon significantly lowers the activation energy for hydrogen-mediated isomerization of P1 to acefluoranthene. This finding could be explained by the specific electronic structures of the transition states and intermediates participating in the isomerization processes. [Figure not available: see fulltext.] © 2010 Springer-Verlag.
URI: https://scidar.kg.ac.rs/handle/123456789/10187
Type: article
DOI: 10.1007/s00894-010-0669-9
ISSN: 1610-2940
SCOPUS: 2-s2.0-77955335340
Appears in Collections:Faculty of Science, Kragujevac

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