8 research outputs found

    Synthesis, spectroscopic characterisation, thermal analysis, DNA interaction and antibacterial activity of copper(I) complexes with N, N′- disubstituted thiourea

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    copper(I) complexes Cu(4MTU)2Cl (2), Cu(4MTU) (B)Cl (3), Cu(6MTU)2Cl (5) and Cu(6MTU) (B)Cl (6) where 4MTU = 1-Benzyl-3-(4-methyl-pyridin-2-yl)-thiourea (1) and 6MTU = 1-Benzyl-3-(6-methyl-pyridin-2-yl)-thiourea (4), B is a N,N-donor heterocyclic base, viz. 1,10-phenanthroline (phen 3, 6), were synthesized, characterized by various physico-chemical and spectroscopic techniques. The elemental analysis suggests that the stoichiometry to be 1:2 (metal:ligand) for 2, 5 1:1:1 (metal:ligand:B) for 3, 6. X-ray powder diffraction illustrates that the complexes have crystalline nature. IR data coupled with electronic spectra and molar conductance values suggest that the complex 2, 5 show the presence of a trigonal planar geometry and the complex 3, 6 show the presence of a tetrahedral geometry about the Cu(I) centre. The binding affinity towards calf thymus (CT) DNA was determined using UV-Vis, fluorescence spectroscopic titrations and viscosity studies. These studies showed that the tested phen complexes 3, 6 bind moderately (in the order of 105 M-1) to CT DNA. The complex 2, 5 does not show any apparent binding to the DNA and hence poor cleavage efficiency. Complex 3, 6 shows efficient oxidative cleavage of plasmid DNA in the presence of H2O2 involving hydroxyl radical species as evidenced from the control data showing inhibition of DNA cleavage in the presence of DMSO and KI. The in vitro antibacterial assay indicates that these complexes are good antimicrobial agents against various pathogens. Anti-bacterial activity is higher when thiourea coordinates to metal ion than the thiourea alone. © 2015 Elsevier B.V

    “In Vitro Antimicrobial Activity and DNA Cleavage Studies: Synthesis and Characterization of Novel M(II) Complexes with O, N, O donor Schiff Base Ligand Derived from Phenylpropanehydrazide”

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    Three new ternary complexes of general formulation [M(L)n] (1–3), where L=N`-(5-chloro-2-hydroxybenzylidine)-3- phenylpropanehydrazide; n=2;M= Cu, Ni, Zn, complexes are synthesized, characterized by various physicochemical and UV-Vis, FTIR, 1H NMR and ESI-MS spectroscopic methods. The Cyclic voltammetry show a quasi-reversible cyclic voltammetric response due to one electron Cu(II)/Cu(I) reduction near 100 mV (versus SCE) in DMF–0.1 M KCl. All the compounds were screened for their in-vitro antibacterial activity against Gram positive and Gram negative bacterial strains. Among them, Cu complex showed good activity against all microbes. The copper complex shows moderate chemical nuclease activity in the presence of MPA as a reducing agen

    In vitro antimicrobial activity and DNA cleavage studies: synthesis and characterization of novel M(II) complexes with tridentate [ONO] donor Schiff base ligand derived from phenylpropane hydrazide

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    Three new ternary complexes of general formulation [M(L)​n] (1-​3)​, where L = N'-​(5-​chloro-​2-​hydroxybenzylidine)​-​3-​phenylpropane hydrazide; n = 2; M = Cu, Ni, Zn, complexes are synthesized, characterized by various physicochem. and UV-​Vis, FT-​IR, 1H NMR and ESI-​MS spectroscopic methods. The Cyclic voltammetry show a quasi-​reversible cyclic voltammetric response due to one electron Cu(II)​/Cu(I) redn. near 100 mV (vs. SCE) in DMF-​0.1 M KCl. All the compds. were screened for their in-​vitro antibacterial activity against Gram pos. and Gram neg. bacterial strains. Among them, Cu complex showed good activity against all microbes. The copper complex shows moderate chem. nuclease activity in the presence of MPA as a reducing agent

    Synthesis, Crystal Structure, Antioxidant, Antimicrobial, and Mutagenic Activities and DNA Interaction Studies of Ni(II) Schiff Base 4-Methoxy-3-Benzyloxybenzaldehyde Thiosemicarbazide Complexes

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    Three new Ni(II) square planar complexes of 4-methoxy-3-benzyloxybenzaldehyde thiosemicarbazide(4m3BTSC) having polypyridyl bases of general formulation [ML2] (1) and [MLB] (2, 3), where L = 4m3BTSC and B is N,N-donor heterocyclic bases, namely, 1,10-phenanthroline (phen, 2), 2,2′-bipyridine (bpy, 3), are synthesized and characterized. The free radical scavenging assay results showed that complex 1 possesses significant activity when compared to complexes 2 and 3. The biological studies showed that the ligand and its complexes exhibited significant and different biological activities and also the prepared compounds are nonmutagenic. They may be potential commercial antioxidants because of their nonmutagenic and nontoxic nature. The DNA interaction of the new complexes is evaluated by absorption, emission, and melting temperature methods, and the results suggested that the binding affinity of the complexes increases with the presence of planar ligand in the molecule. The nickel (II) complexes with planar phenanthroline bases show moderate DNA binding and cleavage ability

    Appraisal of Ground Water Quality in and around Kolar and Malur Taluks of South-Eastern Karnataka, India

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    Atotal of 16 bore well samples were collected from Kolar and Malur taluks and analyzed for physico-chemical and irrigation water quality parameters. Electrical conductivity values indicated that 37.5% of the analyzed water samples were under permissible and doubtful categories and were unsuitable for drinking and irrigation purpose. Total hardness values classified 37.5% of the samples as very hard waters while 81.25% of the samples were non-saline (< 1000 mg L−1) in nature based on total dissolved solids (TDS) levels. Among cations, concentration of alkaline earth metals (Ca+Mg) was dominant over alkali metals (Na+K). Among anions, weak acidic anion (HCO2) concentration was dominant over strong acidic anion concentration (Cl+SO4) in 81.25% of the samples. Majority of the samples were suitable for irrigation purpose based on SAR (Sodium Absorption Ratio) and percent sodium values. WQI (Water Quality Index) values ranged from 7.56 to 24.69 (mean: 14.8) in the study area, which demonstrated their suitability for domestic and other utilitarian purposes. Fluoride content was above the BIS standard limit of 1.5 mg L−1 at Dhanamatanahally, Challahally, Garudnahally, Kolar West and Mangasandra places, which is a matter of concern in view of the health hazards of fluorid

    Novel ligand 1-Benzyl-3-(4-ethyl-pyridin-2-yl)-thiourea and Cu (I) complexes: DNA interaction, antibacterial and thermal studies

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    The new ligand 1-Benzyl-3-(4-ethyl-pyridin-2-yl)-thiourea (1), and two copper(I) complexes Cu(4ETU)2Cl (2), Cu(4ETU)(B)Cl (3) where 4ETU=1-Benzyl-3-(4-ethyl-pyridin-2-yl)-thiourea, B is a N,N-donor heterocyclic base, viz. 1,10-phenanthroline (phen, 3), were synthesized, characterized by various physico-chemical and spectroscopic techniques. The elemental analysis suggests that the stoichiometry to be 1:2 (metal:ligand) for 2 and 1:1:1 (metal:ligand:B) for 3. PXRD analysis provides the crystalline nature of the metal complexes. IR data coupled with electronic spectra and molar conductance values suggest that the complex 2 shows the presence of a trigonal planar geometry and the complex 3 shows the presence of a tetragonal geometry about the Cu(I) centre. Binding interactions of the complexes with calf thymus (CT) DNA have been investigated by absorption, emission, DNA thermal denaturation and viscosity studies. The phen complex displays significant binding propensity to the CT DNA giving an order: 3 (phen) &gt; 2. Complex 3 shows efficient oxidative cleavage of SC-DNA in the presence of H2O2 involving hydroxyl radical species as evidenced from the control data showing inhibition of DNA cleavage in the presence of DMSO and KI. The compounds were screened for their in vitro anti-bacterial activity using Gram-positive bacteria (Staphylococcus aureus, Bacillus subtilis, Micrococcus luteus) and Gramnegative bacteria (Esherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia). Complexes 2 &amp; 3 exhibits higher antibacterial activity against Gram-positive bacteria than the Gram-negative bacteria. Antibacterial activity is higher when thiourea coordinates to metal ion than the thiourea alone. The thermogram of complex 2 exhibits single step and complex 3 exhibits two step decomposition behavior
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