4.5 Article

Synthesis, crystal structure, DNA binding and antitumor studies of β-diketonate complexes of divalent copper, zinc and palladium

Journal

INORGANICA CHIMICA ACTA
Volume 469, Issue -, Pages 76-86

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2017.08.056

Keywords

Isoxazolones; DNA binding; MDA-MB-231; Transition metal complexes; Antimicrobial activity

Funding

  1. University Grants Commission [F1-17.1/2012-13/RGNF-2012-13-ST-AND-18716]

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This paper reports a simple approach for the synthesis of three pairs of novel mononuclear beta-diketonate complexes of copper(II), zinc(II) and palladium(II) from monobasic (OO)-O-Lambda donor ligands 3-phenyl-4-fluorobenzolyl-5-isoxazolone (HL1) and 3-phenyl-4-toluyl-5-isxoazolone (HL2). The synthesized compounds are characterized by FT-IR, ESI/FAB mass, H-1 NMR, UVvisible and thermogravimetric analyses. The free ligand HL1 and the copper(II) complex, [Cu(L-2)(2)(CH3OH)(2)] are unambiguously characterized by single crystal X-ray diffraction studies. The free ligand HL1 has adopted orthorhombic crystal system with P2(1) space group and the unit cell parameters are a = 8.1552(3), b = 10.1169(4), c = 17.0819(6) angstrom, and alpha = beta = gamma = 90 degrees. The crystal structure of the complex, [Cu(L-2)(2)(CH3OH)(2)] is monoclinic with P2(1)/c space group and the unit cell parameters are a = 10.2571(2), b = 16.2640(3), c = 20.1717(3) angstrom, and alpha = 90, beta = 99.56 and gamma = 90 degrees. The copper(II) complex has adopted distorted octahedral geometry where the z-axis is occupied by two solvent methanol molecules according to the crystal data. While the EPR spectra of both the Cu(II) complexes display a strong axial signal with g(3/4) approximate to 2.2 and g(<^>) approximate to 2.0, which obviously suggests the square planar geometry around the copper(II) ion. The interaction of the complexes with calf thymus DNA (CT-DNA) was investigated using UV-visible and fluorescence spectroscopic techniques. Anticancer activity of the complexes revealed their potential towards inhibiting the growth of human breast cancer cell lines, MDA-MB-231. The palladium complexes of both the ligands are found to be good in exhibiting apoptosis. Moreover, the complexes of fluoro-substituted ligand are better antimicrobial agents when compared with those of methyl substituted ligand. (C) 2017 Elsevier B.V. All rights reserved.

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