Synthesis, fluorescent studies, antioxidative and α-amylase inhibitory activity evaluation of some lanthanide(III) complexes

A novel heterocyclic ligand, viz. 1,2-dihydro-1,5-dimethyl-4-[[1-2- -oxo-2H-1-benzopyran-3-yl)ethylidene]amino]-2-phenyl-3H-pyrazol-3-one, was prepared by condensing 3-acetylcoumarin with 4-aminoantipyrine. This ligand is versatile in forming complexes with lanthanum(III), praseodymium(III), samariu...

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Bibliographic Details
Published inJournal of the Serbian Chemical Society Vol. 83; no. 5; pp. 561 - 574
Main Authors Surya, Philip, Preethy, Soosan Thomas, Mohanan, Kochukittan
Format Journal Article
LanguageEnglish
Published Belgrade Journal of the Serbian Chemical Society 01.01.2018
Serbian Chemical Society
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Summary:A novel heterocyclic ligand, viz. 1,2-dihydro-1,5-dimethyl-4-[[1-2- -oxo-2H-1-benzopyran-3-yl)ethylidene]amino]-2-phenyl-3H-pyrazol-3-one, was prepared by condensing 3-acetylcoumarin with 4-aminoantipyrine. This ligand is versatile in forming complexes with lanthanum(III), praseodymium(III), samarium(III), gadolin­ium(III) and dysprosium(III) ions. The ligand and the metal complexes were characterized through various physicochemical and spectral studies. The spec­tral studies revealed that the ligand is coordinated to the metal ion in a biden­tate fashion, through the azomethine nitrogen and the oxygen atom of the pyra­zolone ring. The powder XRD patterns of ligand and the dysprosium(III) com­plex were studied. The photoluminescent properties of ligand and metal com­plexes were evaluated and the relative quantum yields were determined. It was observed that in all cases the metal ions enhanced the luminescence intensity. The α-amylase inhibitory activity of the ligand and the metal complexes was evaluated using the method of Apostolidis. The metal complexes exhibited inc­reased activity compared to the ligand. The antioxidant property was also examined using the DPPH assay and the metal complexes were found to be more potent antioxidants than the ligand.
ISSN:0352-5139
1820-7421
DOI:10.2298/JSC180918010P