Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9902
Full metadata record
DC FieldValueLanguage
dc.rights.licenseBY-NC-ND-
dc.contributor.authorGutman, Ivan-
dc.contributor.authorStojanovska B.-
dc.date.accessioned2021-04-20T14:21:23Z-
dc.date.available2021-04-20T14:21:23Z-
dc.date.issued2011-
dc.identifier.issn1857-5552-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9902-
dc.description.abstractEarlier studies showed that the intensity of cyclic conjugation in the central ring R of perylene can be significantly altered by means of benzo-annelation. In particular, linear (resp. angular) benzoannelation was found to decrease (resp. increase) the intensity of cyclic conjugation in R .We now examine the analogous effect of benzocyclobutadieno-annelation, and show that linear annelation strongly increases the cyclic conjugation in R, whereas the effect of angular annelation is negligibly small.-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceMacedonian Journal of Chemistry and Chemical Engineering-
dc.titleEffect of benzocyclobutadieno-annelation on cyclic conjugation in perylene-
dc.typearticle-
dc.identifier.doi10.20450/mjcce.2011.38-
dc.identifier.scopus2-s2.0-84855298741-
Appears in Collections:Faculty of Science, Kragujevac

Page views(s)

128

Downloads(s)

4

Files in This Item:
File Description SizeFormat 
10.20450-mjcce.2011.38.pdf471.35 kBAdobe PDFThumbnail
View/Open


This item is licensed under a Creative Commons License Creative Commons