Synthesis,characterization of Uranyl(VI), Th(IV), Zr(IV) mixed-ligand complexes with S-methyl-2-(4-methoxybenzylidine)dithiocarbazate and N-donor co-ligand,and their evaluation as antimicrobial agent |
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Authors: | Mohammad Azam Md. Nur Amin Bitu Ranjan K. Mohapatra Saud I. Al-Resayes Lucia Pintilie Saikh Mohammad Wabaidur Fahad Fahhad Alqahtani Mohammad Shahidul Islam Ashish K. Sarangi Md. Kudrat-E-Zahan |
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Affiliation: | 1. Department of Chemistry, College of Science, King Saud University, Riyadh PO BOX 2455, Riyadh 11451, Saudi Arabia;2. Department of Chemistry, University of Rajshahi, Rajshahi 6205, Bangladesh;3. Department of Chemistry, Government College of Engineering, Keonjhar, Odisha 758002, India;4. Department of Synthesis of Bioactive Substances and Pharmaceutical Technologies, National Institute for Chemical & Pharmaceutical Research and Development, Bucharest, Romania;5. Department of Chemistry, School of Applied Sciences, Centurion University of Technology and Management, Odisha, India |
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Abstract: | Schiff base, S-methyl-2-(4-methoxybenzylidine) dithiocarbazate as a primary ligand (HL1), quinoline (L2) as a co-ligand, and hydrated metal salts have been reacted in ethanol in 1:2:1 M ratio to produce mixed-ligand complexes of the type, [M(L1)(L2)].NO3 [M = Uranyl(VI), Th(VI), Zr(IV)], The isolated products have been structurally investigated by elemental analyses, 1H NMR, IR and UV–Vis studies. The electronic studies shows octahedral geometry for all the studied complexes, whereas the molar conductance data suggest an ionic nature. Density functional computation (DFT) studies are also carried out in order to determine the bonding inside the structure of the complexes. The studied mixed-ligand complexes showed moderate antibacterial activity when evaluated against four pathogenic bacteria: Shigella dysenteriae, Bacillus subtilis, Agrobacterium tumefaciens, and Escherichia coli. In addition, molecular docking analysis for all the complexes, using the CLC Drug Discovery Workbench software, showed that they virtually docked on S. dysenteriae, B. subtilis, A. tumefaciens, and E. coli. |
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Keywords: | Molecular docking studies Antibacterial activity Toxicity |
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