Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/16204
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dc.contributor.authorJovanović, Bojanen
dc.contributor.authorMišić-Vukovic M.en
dc.contributor.authorVajs V.en
dc.contributor.authorČanadi, Janošen
dc.date.accessioned2020-03-03T15:03:00Z-
dc.date.available2020-03-03T15:03:00Z-
dc.date.issued1992-01-01en
dc.identifier.issn00222860en
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/16204-
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.en
dc.relation.ispartofJournal of Molecular Structureen
dc.titleSubstituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acidsen
dc.typeJournal/Magazine Articleen
dc.identifier.doi10.1016/0022-2860(92)87065-4en
dc.identifier.scopus2-s2.0-44049115837en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/44049115837en
dc.relation.lastpage414en
dc.relation.firstpage411en
dc.relation.issueCen
dc.relation.volume267en
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFakultet tehničkih nauka, Departman za saobraćaj-
crisitem.author.deptPrirodno-matematički fakultet, Departman za hemiju, biohemiju i zaštitu životne sredine-
crisitem.author.orcid0000-0003-3145-0752-
crisitem.author.parentorgFakultet tehničkih nauka-
crisitem.author.parentorgPrirodno-matematički fakultet-
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