Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12640
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dc.rights.licenseopenAccess-
dc.contributor.authorStanić P.-
dc.contributor.authorRodic, Marko-
dc.contributor.authorV. Soldatovic, Tanja-
dc.contributor.authorPavic A.-
dc.contributor.authorRadakovic N.-
dc.contributor.authorŠmit, Biljana-
dc.contributor.authorZivkovic, Marija-
dc.date.accessioned2021-04-20T21:21:35Z-
dc.date.available2021-04-20T21:21:35Z-
dc.date.issued2020-
dc.identifier.issn0352-5139-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/12640-
dc.description.abstract© 2020 Serbian Chemical Society. All rights reserved. The 3-arylidene-2-thiohydantoin derivative, 3-[(2-hydroxybenzyl-idene)amino]-2-thioxoimidazolidin-4-one, was synthesized in a two-step condensation reaction of 2-hydroxybenzaldehyde, thiosemicarbazide and ethyl chloroacetate. The ligand was structurally characterized by NMR and IR spectroscopy, as well as by elemental analysis. In the reaction of the well-known polymeric trans-[CuCl2(DMSO)2]n complex with the polydentate thiohydantoin type ligand, instead of the corresponding copper thiohydantoin complex, unexpectedly, the dinuclear cis-[{CuCl(DMSO)2}(μ-Cl)]2 complex (1) was formed predominantly as the final stable product. The structure of the complex 1 was confirmed by single crystal X-ray diffraction analysis. The cis-complex is obtained through assisted isomerization of the trans-form, in which the thiohydantoin derivative has a crucial role.-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceJournal of the Serbian Chemical Society-
dc.titleReaction of a 3-aryilidene-2-thiohydantoin derivative with polymeric trans-[CuCl<inf>2</inf>(DMSO)<inf>2</inf>]<inf>n</inf> complex: Unexpected isomerization to dinuclear cis-[{CuCl(DMSO)<inf>2</inf>}(μ-Cl)]<inf>2</inf>-
dc.typearticle-
dc.identifier.doi10.2298/JSC200917060S-
dc.identifier.scopus2-s2.0-85098635360-
Appears in Collections:Faculty of Medical Sciences, Kragujevac
Institute for Information Technologies, Kragujevac

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