A simple mathematical model for the effect of benzoannelation on cyclic conjugation

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DC Field	Value	Language
dc.rights.license	BY-NC-ND	-
dc.contributor.author	Gutman, Ivan	-
dc.contributor.author	Balaban A.	-
dc.date.accessioned	2021-04-20T14:26:02Z	-
dc.date.available	2021-04-20T14:26:02Z	-
dc.date.issued	2011	-
dc.identifier.issn	0352-5139	-
dc.identifier.uri	https://scidar.kg.ac.rs/handle/123456789/9931	-
dc.description.abstract	In a series of earlier studies, it was established that benzoannelation in the angular (resp. linear) position relative to a ring R of a polycyclic conjugated π-electron system, increases (resp. decreases) the intensity of the cyclic conjugation in the ring R. Herein, it is shown how this regularity can be explained by means of a simple, Kekulé-structurebased argument, itself based on an idea of Randić from the 1970s.	-
dc.rights	openAccess	-
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/4.0/	-
dc.source	Journal of the Serbian Chemical Society	-
dc.title	A simple mathematical model for the effect of benzoannelation on cyclic conjugation	-
dc.type	article	-
dc.identifier.doi	10.2298/jsc110224131g	-
dc.identifier.scopus	2-s2.0-80054976954	-
Appears in Collections:	Faculty of Science, Kragujevac

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