Synthesis and Characterization of Some New Cu(II), Ni(II) and Zn(II) Complexes with Salicylidene Thiosemicarbazones: Antibacterial, Antifungal and in Vitro Antileukemia Activity

dc.contributor.authorPahonțu, Elena
dc.contributor.authorFala, Valeriu
dc.contributor.authorGulea, Aurelian
dc.contributor.authorPoirier, Donald
dc.contributor.authorTapcov, Victor
dc.contributor.authorRosu, Tudor
dc.date.accessioned2016-10-26T08:43:18Z
dc.date.available2016-10-26T08:43:18Z
dc.date.issued2013
dc.description.abstractThirty two new Cu(II), Ni(II) and Zn(II) complexes (1–32) with salicylidene thiosemicarbazones (H2L1–H2L10) were synthesized. Salicylidene thiosemicarbazones, of general formula (X)N-NH-C(S)-NH(Y), were prepared through the condensation reaction of 2-hydroxybenzaldehyde and its derivatives (X) with thiosemicarbazide or 4-phenylthiosemicarbazide (Y = H, C6H5). The characterization of the new formed compounds was done by 1H-NMR, 13C-NMR, IR spectroscopy, elemental analysis, magnetochemical, thermoanalytical and molar conductance measurements. In addition, the structure of the complex 5 has been determined by X-ray diffraction method. All ligands and metal complexes were tested as inhibitors of human leukemia (HL-60) cells growth and antibacterial and antifungal activities.en
dc.identifier.citationGULEA, Au., TAPCOV, Vl. et al. Synthesis and characterization of some new Cu(II), Ni(II) and Zn(II) complexes with salicylidene thiosemicarbazones:antibacterial, antifungal and in vitro antileukemia activity. In: Molecules. 2013, Vol.18, Issue 8, pp.8812-8836en
dc.identifier.issn1420-3049
dc.identifier.urihttps://msuir.usm.md/handle/123456789/890
dc.language.isoenen
dc.publisherMolecular Diversity Preservation International (MDPI)en
dc.subjectcopperen
dc.subjectnickelen
dc.subjectzinc complexesen
dc.subjectthiosemicarbazonesen
dc.subjectantimicrobial activityen
dc.subjectantileukemiaen
dc.titleSynthesis and Characterization of Some New Cu(II), Ni(II) and Zn(II) Complexes with Salicylidene Thiosemicarbazones: Antibacterial, Antifungal and in Vitro Antileukemia Activityen
dc.typeArticleen

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