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dc.contributor.authorOzturk, I. I.en
dc.contributor.authorHadjikakou, Sotiris K.en
dc.contributor.authorHadjiliadis, Nicken
dc.contributor.authorKourkoumelis, Nikolaosen
dc.contributor.authorKubicki, Maciejen
dc.contributor.authorTasiopoulos, Anastasios J.en
dc.contributor.authorScleiman, H.en
dc.contributor.authorBarsan, M. M.en
dc.contributor.authorButler, I. S.en
dc.contributor.authorBalzarini, J.en
dc.creatorOzturk, I. I.en
dc.creatorHadjikakou, Sotiris K.en
dc.creatorHadjiliadis, Nicken
dc.creatorKourkoumelis, Nikolaosen
dc.creatorKubicki, Maciejen
dc.creatorTasiopoulos, Anastasios J.en
dc.creatorScleiman, H.en
dc.creatorBarsan, M. M.en
dc.creatorButler, I. S.en
dc.creatorBalzarini, J.en
dc.date.accessioned2019-11-21T06:21:51Z
dc.date.available2019-11-21T06:21:51Z
dc.date.issued2009
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55930
dc.description.abstractNew antimony(III) bromide complexes with the heterocyclic thioamides, thiourea (TU), 2-mercapto-1-methylimidazole (MMl), 2-mercapto-benzimidazole (MBZlM), 2-mercapto-5-methyl-benzimidazole (MMBZIM), 5-ethoxy-2-mercapto- benzimidazole (EtMBZIM), 2-mercapto-3,4,5,6-tetrahydro-pyrimidine (tHPMT), 2-mercaptopyridine (PYT), 2-mercapto-thiazolidine (MTZD), 3-methyl-2- mercaptobenzothiazole (MMBZT), and 2-mereaptopyrimidine (PMTH) of formulas [SbBr3(TU)2] (1), [SbBr3(MMI)2] (2), {[SbBr2(MBZIM)4]+ [Br]- H20} (3), {[SbBr2(μ2-Br)(MMBZIM)2]2} (4), {[SbBr2(μ2μ-Br)(EtMBZIM)2]2 MeOH} (5), {[SbBr3(μ2-S-tHPMT)(tHPMT)]n} (6), {[SbBr2(μ2-Br)(PYT)2)n} (7), {[SbBr2(μ2μ-Br)(MTZD)2]n} (8), [SbBr3(MMBZT)2] (9), and {[SbBr5] 2-[(PMTH2 ++)2 +]} (10) have been synthesized and characterized by elemental analysis, conductivity measurements, FTlR spectroscopy, FT-Raman spectroscopy, TG-DTA analysis, and X-ray powder diffraction. The crystal structures of 3, 4, 5, 6, 7, 8, and 10 were also determined by X-ray diffraction. In 3, four sulfur atoms from thione ligands and two bromide ions form an octahedral (Oh) cationic [SbS4Br2]++ species in which the two bromide anions lie at axial positions. A third bromide counteranion neutralizes the whole complex. 4 and 5 are dimers, whereas 6,7 and 8 are polymers, built up by monomeric units of square pyramidal (SP) geometry around the metal center, which were formed by two sulfur atoms of thioamide ligands and three bromide ions. Finally, 10 is ionic salt containing 1D polymeric network of {[SbBr 5]2-}n anions and -[(PMTH 2 ++)2] counter cations in the lattice. The complexes showed mostly a moderate cytostatic activity against a variety of tumor cell lines. © 2009 American Chemical Society.en
dc.sourceInorganic chemistryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-64649091664&doi=10.1021%2fic8019205&partnerID=40&md5=2c3bb76f021f5c29ad1a26b9f3e94784
dc.subjectarticleen
dc.subjecthumanen
dc.subjectHumansen
dc.subjectdrug effecten
dc.subjectcell proliferationen
dc.subjectAnimalsen
dc.subjectanimalen
dc.subjectchemistryen
dc.subjectcytostatic agenten
dc.subjectcomputer simulationen
dc.subjectsynthesisen
dc.subjectchemical structureen
dc.subjectX ray crystallographyen
dc.subjectantimonyen
dc.subjecttumor cell lineen
dc.subjectorganometallic compounden
dc.subjectOrganometallic Compoundsen
dc.subjectCell Line, Tumoren
dc.subjectModels, Molecularen
dc.subjectCrystallography, X-Rayen
dc.subjectCytostatic Agentsen
dc.subjectbromideen
dc.subjectBromidesen
dc.subjectthioamideen
dc.subjectThioamidesen
dc.titleNew antimony(III) bromide complexes with thioamides: Synthesis, characterization, and cytostatic propertiesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1021/ic8019205
dc.description.volume48
dc.description.issue5
dc.description.startingpage2233
dc.description.endingpage2245
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.source.abbreviationInorg.Chem.en
dc.contributor.orcidTasiopoulos, Anastasios J. [0000-0002-4804-3822]
dc.contributor.orcidHadjikakou, Sotiris K. [0000-0001-9556-6266]
dc.gnosis.orcid0000-0002-4804-3822
dc.gnosis.orcid0000-0001-9556-6266


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