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dc.contributor.authorKavitha, P.-
dc.contributor.authorSaritha, M.-
dc.contributor.authorLaxma Reddy, K.-
dc.date.accessioned2025-01-01T05:10:33Z-
dc.date.available2025-01-01T05:10:33Z-
dc.date.issued2013-02-
dc.identifier.citation10.1016/j.saa.2012.10.037en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2274-
dc.descriptionNITWen_US
dc.description.abstractCu(II) complexes have been synthesized from different Schiff bases, such as 3-((2-hydroxy phenylimino)methyl)-4H-chromen-4-one (HL1), 2-((4-oxo-4H-chromen-3-yl)methylneamino) benzoicacid (HL2), 3-((3-hydroxypyridin-2-ylimino)methyl)-4H-chromen-4-one (HL3) and 3-((2-mercaptophenylimino)methyl)-4H-chromen-4-one (HL4). The complexes were characterized by analytical, molar conductance, IR, electronic, magnetic, ESR, thermal, powder XRD and SEM studies. The analytical data reveal that metal to ligand molar ratio is 1:2 in all the complexes. Molar conductivity data indicates that all the Cu(II) complexes are neutral. On the basis of magnetic and electronic spectral data, distorted octahedral geometry is proposed for all the Cu(II) complexes. Thermal behaviour of the synthesized complexes illustrates the presence of lattice water molecules in the complexes. X-ray diffraction studies reveal that all the ligands and their Cu(II) complexes have triclinic system with different unit cell parameters. Antimicrobial, antioxidant and DNA cleavage activities indicate that metal complexes exhibited greater activity as compared with ligands.en_US
dc.language.isoenen_US
dc.publisherSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopyen_US
dc.subjectAntimicrobial activityen_US
dc.subjectAntioxidanten_US
dc.subjectDNA cleavageen_US
dc.subjectFluorescenceen_US
dc.titleSynthesis, structural characterization, fluorescence, antimicrobial, antioxidant and DNA cleavage studies of Cu(II) complexes of formyl chromone Schiff basesen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

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