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dc.contributor.authorAlyar, Saliha
dc.contributor.authorZengin, Huseyin
dc.contributor.authorOzbek, Neslihan
dc.contributor.authorKaracan, Nurcan
dc.date.accessioned2019-11-24T20:35:28Z
dc.date.available2019-11-24T20:35:28Z
dc.date.issued2011
dc.identifier.issn0022-2860
dc.identifier.urihttps://dx.doi.org/10.1016/j.molstruc.2011.02.024
dc.identifier.urihttps://hdl.handle.net/20.500.12513/1861
dc.descriptionWOS: 000289965000004en_US
dc.description.abstractNew aryldisulfonamides were synthesized and characterized by FTIR, (1)H NMR, (13)C NMR, HETCOR, COSY, LC-MS and elemental analysis techniques. The compounds gave intense emissions, where lambda(max) = 405, 379 and 402 nm, upon irradiation by Ultra-Violet light. The photoluminescence quantum yields and long excited-state lifetimes of the compounds were calculated and were found to have photoluminescence quantum yields 39 +/- 1.8%, 45 +/- 2.2% and 34 +/- 1.4% and long excited-state lifetimes of 3.65 +/- 0.16, 4.17 +/- 0.20 and 3.15 +/- 0.12 ns, respectively. The photoluminescence intensities and quantum yields of compounds varied with the position of substituent on the ring and the chain length between aromatic rings. These novel compounds may be of interest as organic emitting materials for electroluminescent devices. The visible absorption maxima were calculated using time-depended density-functional theory (ID-OFT) and Zerner's intermediate neglect of differential overlap/spectroscopic (ZINDO/S) method in the gas phase. Further, the compounds were evaluated for in vitro antimicrobial activity against various microorganisms by microdilution and disk diffusion methods. (C) 2011 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipTUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [TBAG 104 T 390, MAG 104M 367]; Gazi University Scientific Research ProjectGazi University [05/2008-05]en_US
dc.description.sponsorshipThe authors wish to thank TUBITAK for the financial support (TBAG 104 T 390 and (MAG 104M 367) and Gazi University Scientific Research Project (05/2008-05). We would also like to thank the Departments of Chemistry at Gazi University and Gaziantep University.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.relation.isversionof10.1016/j.molstruc.2011.02.024en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDisulfonamidesen_US
dc.subjectPhotoluminescenceen_US
dc.subjectAntimicrobial activityen_US
dc.subjectTD-DFT/B3LYP calculationsen_US
dc.subjectZINDO/S calculationsen_US
dc.titleSynthesis, characterization, spectroscopic properties, theoretical calculation, and antimicrobial activity of new aryldisulfonamidesen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF MOLECULAR STRUCTUREen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Eğitim Fakültesi, İlköğretim Bölümüen_US
dc.identifier.volume992en_US
dc.identifier.issue1.Maren_US
dc.identifier.startpage27en_US
dc.identifier.endpage32en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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