Приказ основних података о документу

dc.creatorJovanović, Slobodanka
dc.creatorMijin, Dušan
dc.creatorMisić-Vuković, Milica
dc.date.accessioned2021-03-10T10:33:55Z
dc.date.available2021-03-10T10:33:55Z
dc.date.issued2006
dc.identifier.issn1551-7004
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/945
dc.description.abstractSpectral characteristics of the two series of previously synthesized and identified 4,6-disubstituted- 3-cyano-2-pyridones were determined, and corresponding H-1 NMR chemical shifts and IR and UV frequencies were correlated with LFER parameters. A variety of substituents were employed for both alkyl and aryl substitution, and fairly good correlations were obtained, using simple Hammett and Hammett-Taft dual parameter equations, as well as the more sophisticated multiparameter regression approaches. It was established that both polar and steric effects influence the spectra of the investigated compounds.en
dc.publisherArkat Usa Inc, Gainesville
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142063/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArkivoc
dc.subjectsubstituted 2-pyridonesen
dc.subjectLFER analysisen
dc.subjectIRen
dc.subjectNMR and UV spectraen
dc.titleCorrelation analysis of IR, H-1 NMR and UV spectral data of alkyl and aryl 4,6-disubstituted-3-cyano-2-pyridones. Part Ien
dc.typearticle
dc.rights.licenseBY
dc.citation.epage128
dc.citation.other: 116-128
dc.citation.spage116
dc.identifier.doi10.3998/ark.5550190.0007.a15
dc.identifier.fulltexthttp://TechnoRep.tmf.bg.ac.rs/bitstream/id/2383/942.pdf
dc.identifier.wos000244431900015
dc.type.versionpublishedVersion


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Приказ основних података о документу