4.7 Article

Synthesis of new piperazine derived Cu(II)/Zn(II) metal complexes, their DNA binding studies, electrochemistry and anti-microbial activity: Validation for specific recognition of Zn(II) complex to DNA helix by interaction with thymine base

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2008.12.037

Keywords

UV-vis titrations; Fluorescence; Cyclic voltammetry; Antimicrobial activity; Viscosity measurements

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Funding

  1. Third World Academy of Science, Italy [01-268RG/CHE/AS]
  2. University Grants Commission. New Delhi [31-100/2005]

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New 3,41:9,10-dibenzo-2,11-dihydroxy-1,12-bispiperazine-5,8-dioxododecane complexes [C24H36N4O6Cu] (1), [C24H32N4O4Zn] (2) have been synthesized and characterized by elemental analysis, IR, NMR, Mass, EPR. UV-vis spectroscopy and Molar conductance measurements. The complexes are non-ionic in nature and possess octahedral geometry around Cu2+, Zn2+ central metal ions. The binding studies of I and 2 with calf thymus DNA (CT-DNA) were investigated by UV-vis, fluorescence, cyclic voltammetery and viscosity measurements. The calculated binding constant K-b for 1 and 2 obtained from UV-vis absorption studies was 7.6 x 10(3) M-1, 80.8 x 10(4) M-1, respectively. The intrinsic binding constants were also estimated to be 7.0 x 10(4) M-1 and 7.53 x 10(5) M-1 for 1 and 2, respectively by using emission titrations. These experimental results Suggest that complexes are groove binders and interact to CT-DNA with different affinities. Both the complexes in presence and absence of CT-DNA show quasireversible wave Corresponding to Cu-II/Cu-I and Zn-II/Zn-I redox Couple. The changes in E-1/2, Delta E. I-pa/I-pc ascertain the interaction of 1 and 2 with CT-DNA. Further, decrease in viscosity of CT-DNA with increasing concentration of complexes was observed. In vitro. antimicrobial activity against fungi A. brassicicola, A. niger and bacteria E. coli, P. aeruginosa of complexes were carried out, which indicate that complex 2 is more active against both fungal and bacterial strains as shown by % inhibition data. (C) 2008 Elsevier B.V. All rights reserved.

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