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Solvatohromizam N-aril-fenilacetamida

dc.creatorMatijević, Borko M.
dc.creatorMrđan, Gorana S.
dc.creatorVaštag, Đenđi
dc.creatorApostolov, Suzana
dc.creatorNikolić, Jovana
dc.creatorMarinković, Aleksandar
dc.date.accessioned2021-03-10T12:59:32Z
dc.date.available2021-03-10T12:59:32Z
dc.date.issued2016
dc.identifier.issn0351-9465
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/3213
dc.description.abstractAmide derivates are biologically active compounds and they are widely used in all spheres of life. Therefore, it is very important to know their physical-chemical properties. In this work the influence of characteristics and nature of the solvent on the absorption spectra of N-aryl-phenylacetamide was investigated, in order to obtain information about their solvatochromic properties. The spectra of the compounds were recorded in 15 solvents, with different properties, in the wavelength range from 200 to 400 nm. The effect of the solvents on the absorption spectra of N-aryl-phenylacetamide was analyzed by using Kamlet-Taft's solvatochromic model. Also, in order to obtain detailed information on the type and dominance of the interactions that occur between the compound and the surrounding medium, correlations were made with absorption maxima and Hansen's solvent parameters. In addition to the effect of solvent, the impact of the chemical structure on the spectral behavior of tested amide derivatives was analyzed.en
dc.description.abstractDerivati amida su biološki aktivna jedinjenja i imaju široku primenu u svim sferama života. Zbog toga je veoma važno poznavati njihova fizičko-hemijska svojstva. U ovom radu ispitivan je uticaj osobina i prirode rastvarača na apsorpcione spektre N-aril-fenilacetamida radi dobijanja informacija o njihovim solvatohromnim svojstvima. Spektri ispitivanih jedinjenja su snimljeni u 15 rastvarača različitih osobina, u opsegu talasnih dužina od 200 do 400 nm. Uticaj rastvarača na apsorpcione spektre N-aril-fenilacetamida analiziran je pomoću Kamlet-Taft-ovog solvatohromnog modela. Takođe, radi dobijanja detaljnijih informacija o vrsti i dominantnosti interakcija koje se javljaju između jedinjenja i okolnog medijuma, urađene su korelacije apsorpcionih maksimuma sa Hansen-ovim parametrima rastvarača. Pored uticaja rastvarača analiziran je i uticaj hemijske strukture na spektralno ponašanje ispitivanih derivata amida.sr
dc.publisherEngineering Society for Corrosion, Belgrade, Serbia
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceZaštita materijala
dc.subjectN-phenylacetamideen
dc.subjectsolvatochromismen
dc.subjectKamlet-Taften
dc.subjectHansenen
dc.subjectspektrohhotometric metodsen
dc.subjectN-fenilacetamidisr
dc.subjectsolvatohromizamsr
dc.subjectKamlet-Taftsr
dc.subjectHansensr
dc.subjectspektrofotometrijasr
dc.titleSolvatochromism of N-aryl-phenylacetamidesen
dc.titleSolvatohromizam N-aril-fenilacetamidasr
dc.typearticle
dc.rights.licenseBY-NC-ND
dc.citation.epage264
dc.citation.issue2
dc.citation.other57(2): 253-264
dc.citation.rankM24
dc.citation.spage253
dc.citation.volume57
dc.identifier.doi10.5937/ZasMat1602253M
dc.identifier.fulltexthttp://TechnoRep.tmf.bg.ac.rs/bitstream/id/9409/0351-94651602253M.pdf
dc.type.versionpublishedVersion


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