Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/17336
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dc.contributor.authorGutman, Ivan-
dc.contributor.authorFurtula, Boris-
dc.contributor.authorGlišić, Biljana-
dc.contributor.authorMarković, Violeta-
dc.contributor.authorVesel, Aleksander-
dc.date.accessioned2023-03-16T11:45:22Z-
dc.date.available2023-03-16T11:45:22Z-
dc.date.issued2007-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/17336-
dc.description.abstractA structure-descriptor EE, recently proposed by Estrada, is examined. If λ₁, λ₂,..., λո are the eigenvalues of the molecular graph, then EE=Ʃeλi . In the case of trees with n vertices (that are the graph representations of alkane isomers CռH2ռ₊₂), the main structural factor influencing the differences between the EE-values has been found to be the Zagreb index Zg. The coefficient b in the regression line EE = a Zg + b is an almost perfectly linear function of n, implying that in the case of alkanes, EE linearly increases with the number of carbon atoms.en_US
dc.language.isoen_USen_US
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.sourceIndian Journal of Chemistry A-
dc.titleEstrada index of acyclic moleculesen_US
dc.typearticleen_US
dc.description.versionPublisheden_US
dc.type.versionPublishedVersionen_US
Appears in Collections:Faculty of Science, Kragujevac

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