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dc.creatorJovanović, Bratislav Ž.
dc.creatorMišić-Vuković, Milica M.
dc.creatorVajs, Vlatka
dc.creatorČanadi, J. J.
dc.date.accessioned2019-04-30T21:44:04Z
dc.date.available2019-04-30T21:44:04Z
dc.date.issued1992
dc.identifier.issn0022-2860
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2789
dc.description.abstractThe 13C N.M.R. spectra of some substituted α-phenylpyridylacrylic acids, α-phenyl, α-(3-pyrydyl) and α-(3-pyrydyl-N-oxide) cinnamic acids were determined in deuterated dimethyl sulfoxide (d6-DMSO). It has been shown that the subsitutent chemical shifts (SCS) for Cβatom ethylenic bond of the examined compounds correlated linearely with the summ of the corresponding substituent constants in the both rings (σx + σY). This correlation was interpreted as evidence that the electronic effects of both substituents are involved in conjugated aromatic system. © 1992.
dc.publisherElsevier Science Publishers B.V.
dc.rightsrestrictedAccess
dc.sourceJournal of Molecular Structure
dc.titleSubstituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractВајс, Влатка; Јовановић, Б. Ж.; Мишић-Вуковиц, М.; Чанади, Ј. Ј.;
dc.rights.holderElsevier
dc.citation.volume267
dc.citation.issueC
dc.citation.spage411
dc.citation.epage414
dc.identifier.doi10.1016/0022-2860(92)87065-4
dc.identifier.scopus2-s2.0-44049115837
dc.type.versionpublishedVersion


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