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dc.contributor.authorKantar, Cihan
dc.contributor.authorMavi, Vildan
dc.contributor.authorBaltaş, Nimet
dc.contributor.authorİslamoğlu, Fatih
dc.contributor.authorŞaşmaz, Selami
dc.date.accessioned2020-12-19T19:50:04Z
dc.date.available2020-12-19T19:50:04Z
dc.date.issued2016
dc.identifier.citationKantar, C., Mavi, V., Baltas, N., Islamoglu, F., Sasmaz, S. (2016). Novel zinc(II)phthalocyanines bearing azo-containing schiff base: Determination of pKa values, absorption, emission, enzyme inhibition and photochemical properties. Journal of Molecular Structure, 1122, 88-99. https://doi.org/10.1016/j.molstruc.2016.05.055en_US
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2016.05.055
dc.identifier.urihttps://hdl.handle.net/11436/2378
dc.descriptionSasmaz, Selami/0000-0001-5311-7550; kantar, cihan/0000-0002-5234-0782en_US
dc.descriptionWOS: 000381167800011en_US
dc.description.abstractAzo-containing schiff bases are well known and there are many studies about their various properties in literature. However, phthalocyanines bearing azo-containing schiff bases, their spectral, analytical and biological properties are unknown. Therefore, new zinc (II) phthalocyanines bearing azo-containing schiff base were synthesized and investigated to determine pKa values, absorption, emission, enzyme inhibition and photochemical properties. Emission spectra were reported and large Stokes shift values were determined for all compounds, indicating that all molecules exhibit excited state intramolecular proton transfer. These phthalocyanines were the first examples of phthalocyanine showing excited state intramolecular proton transfer. Singlet oxygen quantum yields of zinc (II) phthalocyanines were determined. pKa values and indicator properties of all compounds were investigated by potentiometry. All compounds were assayed for inhibitory activity against bovine milk xanthine oxidase and acetylcholinesterase enzyme in vitro. Compound 2 showed the high inhibitory effect against xanthine oxidase (IC50 = 0.24 +/- 0.01 mu M). However, phthalocyanine compounds did not show enzyme inhibitor behavior. (C) 2016 Elsevier B.V. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPhthalocyaninesen_US
dc.subjectAzoen_US
dc.subjectSchiff baseen_US
dc.subjectESIPTen_US
dc.subjectEnzyme inhibitionen_US
dc.titleNovel zinc(II)phthalocyanines bearing azo-containing schiff base: Determination of pKa values, absorption, emission, enzyme inhibition and photochemical propertiesen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Fen - Edebiyat Fakültesi, Kimya Bölümüen_US
dc.contributor.institutionauthorKantar, Cihan
dc.contributor.institutionauthorMavi, Vildan
dc.contributor.institutionauthorBaltaş, Nimet
dc.contributor.institutionauthorİslamoğlu, Fatih
dc.contributor.institutionauthorŞaşmaz, Selami
dc.identifier.doi10.1016/j.molstruc.2016.05.055
dc.identifier.volume1122en_US
dc.identifier.startpage88en_US
dc.identifier.endpage99en_US
dc.relation.journalJournal of Molecular Structureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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