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dc.contributor.authorMuglu, Halit
dc.contributor.authorCavus, M. Serdar
dc.contributor.authorBakir, Temelkan
dc.contributor.authorYakan, Hasan
dc.date.accessioned2020-06-21T12:19:57Z
dc.date.available2020-06-21T12:19:57Z
dc.date.issued2019
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2019.07.002
dc.identifier.urihttps://hdl.handle.net/20.500.12712/10486
dc.descriptioncavus, Muhammet Serdar/0000-0002-3721-0883en_US
dc.descriptionWOS: 000487930600082en_US
dc.description.abstract1,5-Bis(5-chloro-2-oxoindolin-3-ylidene)thiocarbohydrazone (3), 1,5-Bis(5-metoxy-2-oxoindolin-3-ylidene)thiocarbohydrazone (4), 1,5-Bis(5-metoxy-2-oxoindolin-3-ylidene)carbohydrazone (5) were obtained from isatins and thio/carbohydrazides under reflux in absolute ethanol. The structures of these synthesized compounds were determined using FT-IR, H-1 NMR, C-13 NMR spectroscopy, and elemental analysis. Quantum chemical calculations were also performed at B3LYP/6-311++G(2d,2p) level in order to obtain information about the molecular geometries and electronic data, such as HOMO-LUMO energy eigenvalues and density of states (DOSs). In addition, structural and antioxidant properties of the compounds were studied theoretically. QTAIM analysis was performed to investigate the relationship between intramolecular interactions, electronic data and antioxidant activity. The in vitro antioxidant activity of all the compounds was determined by 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging method. Antioxidant activity was followed by Ascorbic acid > 3 > 4 > 5. (C) 2019 Elsevier B.V. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.molstruc.2019.07.002en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectIsatinen_US
dc.subjectCarbohydrazideen_US
dc.subjectAntioxidant activityen_US
dc.subjectDFTen_US
dc.subjectQTAIMen_US
dc.subjectSpectroscopic techniquesen_US
dc.titleSynthesis, characterization, quantum chemical calculations and antioxidant activity of new bis-isatin carbohydrazone and thiocarbohydrazone derivativesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume1196en_US
dc.identifier.startpage819en_US
dc.identifier.endpage827en_US
dc.relation.journalJournal of Molecular Structureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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