Synthesis, Structural Characterization, and Antibacterial Activity of Cu(II) and Zn(II) Complexes With Tetradentate Schiff Bases

References

• Tehrani, K. H. M. E.; Sardari, S.; Mashayekhi, V.; Zadeh, M. E.; Azerang, P.; Kobarfard, F. One pot synthesis and biological activity evaluation of novel Schiff bases derived from 2-hydrazinyl-1,3,4-thiadiazole. Chem. Pharm. Bull. 2013, 61, 160–166.
   PubMed Web of Science ®Google Scholar
• Sallam, S. A.; Ibrahim, E. S. I.; Anwar, M. I. Synthesis, complexation and biological activity of new Isatin-Schiff bases. J. Chil. Chem. Soc. 2012, 57, 1482–1491.
   Web of Science ®Google Scholar
• Azizian, J.; Mohammadi, M. K.; Firuzi, O.; Razzaghi-asl, N.; Miri, R. Synthesis, biological activity and docking study of some new isatin Schiff base derivatives. Met. Chem. Res. 2012, 21, 3730–3740.
   Web of Science ®Google Scholar
• Makawana, J. A.; Sun, J.; Zhu, H.-L. Schiff's base derivatives bearing nitroimidazole moiety: New class of antibacterial, anticancer agents and potential EGFR tyrosine kinase inhibitors. Bioorg. Med. Chem. Lett. 2013, 23, 6264–6268.
   PubMed Web of Science ®Google Scholar
• El-Sherif, A. A.; Aljahdali, M. S. Review: protonation, complex-formation equilibria, and metal-ligand interaction of salicylaldehyde Schiff bases. J. Coord. Chem. 2013, 66, 3423–3468.
   Web of Science ®Google Scholar
• Islam, S. M.; Paul, S.; Roy, A. S.; Banerjee, S.; Mobarok, M.; Santra, S. C. Synthesis, catalytic activity and phytotoxicity of a supported nickel(II) Schiff base complex. Transition Met. Chem. 2013, 38, 855–864.
   Web of Science ®Google Scholar
• Maiti, M.; Thakurta, S.; Sadhukhan, D.; Pilet, G.; Rosair, G. M.; Nonat, A.; Charbonniere, L. J.; Mitra, S. Thermally stable luminescent zinc-Schiff base complexes: A thiocyanato bridged 1D coordination polymer and a supramolecular 1D polymer. Polyhedron 2013, 65, 6–15.
   Web of Science ®Google Scholar
• Rosu, T.; Pahontu, E.; Ilies, D.-C.; Georgescu, R.; Mocanu, M.; Leabu, M.; Shova, S.; Gulea, A. Synthesis and characterization of some new complexes of Cu(II), Ni(II) and V(IV) with Schiff base derived from indole-3-carboxaldehyde. Biological activity on prokaryotes and eukaryotes. Eur. J. Med. Chem. 2012, 53, 380–389.
   PubMed Web of Science ®Google Scholar
• Zhao, X.-J.; Xue, L.-W.; Zhao, G.-Q. Synthesis, structures, and antimicrobial activities of dimeric oxovanadium(V) complexes with tridentate Schiff bases. Synth. React. Inorg. Met.-Org. Nano-Met. Chem. 2013, 43, 1344–1348.
   Web of Science ®Google Scholar
• Patel, R. N.; Singh, A.; Sondhiya, V. P.; Singh, Y.; Shukla, K. K.; Patel, D. K.; Pandey, R. Synthesis, characterization, and biological activity of nickel(II) complexes with a tridentate Schiff base derived from heterocyclic aldehyde. J. Coord. Chem. 2012, 65, 795–812.
   Web of Science ®Google Scholar
• Mobinikhaledi, A.; Zendehdel, M.; Safari, P.; Hamta, A.; Shariatzadeh, S. M. Synthesis and biological activity evaluation of some binuclear metal complexes of Cu(II) and Zn(II) with tridentate Schiff base ligands. Synth. React. Inorg. Met.-Org. Nano-Met. Chem. 2012, 42, 165–170.
   Web of Science ®Google Scholar
• Ghosh, M.; Fleck, M.; Mahanti, B.; Ghosh, A.; Pilet, G.; Bandyopadhyay, D. Syntheses, crystal structures, and antibacterial activities of manganese(III), nickel(II), and copper(II) complexes containing a tetradentate Schiff base. J. Coord. Chem. 2012, 65, 3884–3894.
   Web of Science ®Google Scholar
• Joseph, J.; Mary, N. L.; Sidambaram, R. Synthesis, characterization, and antibacterial activity of the Schiff bases derived from thiosemicarbazide, salicylaldehyde, 5-bromosalicylaldehyde and their Copper(II) and Nickel(II) complexes. Synth. React. Inorg. Met.-Org. Nano-Met. Chem. 2010, 40, 930–933.
   Web of Science ®Google Scholar
• You, Z.-L.; Zhu, H.-L. Syntheses, crystal structures, and antibacterial activities of four Schiff base copper(II), zinc(II), and cadmium(II) complexes derived from 2-[(2-dimethylaminoethylimino)methyl]phenol. Z. Anorg. Allg. Chem. 2006, 632, 140–146.
   Web of Science ®Google Scholar
• Chohan, Z. H.; Arif, M.; Shafiq, Z.; Yaqub, M.; Supuran, C. T. In vitro antibacterial, antifungal & cytotoxic activity of some isonicotinoylhydrazide Schiff's bases and their cobalt(II), copper(II), nickel(II) and zinc(II) complexes. J. Enzyme Inhib. Med. Chem. 2006, 21, 95–103.
   PubMed Web of Science ®Google Scholar
• Bruker. SAINT Software Reference Manual; Bruker AXS, Madison, WI, 1998.
   Google Scholar
• Sheldrick, G. M. SADABS, Siemens Area Detector Absorption Corrected Software; University of Göttingen, Germany, 1996.
   Google Scholar
• Sheldrick, G. M. SHELXTL NT Version 5.1. Program for Solution and Refinement of Crystal Structures; University of Göttingen, Germany, 1997.
   Google Scholar
• Rosu, T.; Pahontu, E.; Pasculescu, S.; Georgescu, R.; Stanica, N.; Curaj, A.; Popescu, A.; Leabu, M. Synthesis, characterization antibacterial and antiproliferative activity of novel Cu(II) and Pd(II) complexes with 2-hydroxy-8-R-tricyclo[7.3.1.0.2,7]. Eur. J. Med. Chem. 2010, 45, 1627–1634.
   PubMed Web of Science ®Google Scholar
• Geary, W. J. Use of conductivity measurements in organic solvents for characterisation of coordination compounds. Coord. Chem. Rev. 1971, 7, 81–122.
   Web of Science ®Google Scholar
• Rayati, S.; Zakavi, S.; Koliaei, M.; Wojtczak, A.; Kozakiewicz, A. Electron-rich salen-type Schiff base complexes of Cu(II) as catalysts for oxidation of cyclooctene and styrene with tert-butylhydroperoxide: a comparison with electron-deficient ones. Inorg. Chem. Commun. 2010, 13, 203–207.
   Web of Science ®Google Scholar
• Naiya, S.; Biswas, C.; Drew, M. G. B.; Gomez-Garcia, C.-J.; Clemente-Juan, J. M.; Ghosh, A. A unique example of structural and magnetic diversity in four interconvertible copper(II)-azide complexes with the same Schiff base ligand: A monomer, a dimer, a chain, and a layer. Inorg. Chem. 2010, 49, 6616–6627.
   PubMed Web of Science ®Google Scholar
• Chu, Z. L.; Huang, W.; Wang, L.; Gou, S. H. Chiral 27-membered [3+3] Schiff-base macrocycles and their reactivity with first-row transition metal ions. Polyhedron 2008, 27, 1079–1092.
   Web of Science ®Google Scholar
• Gao, J.; Liu, Y. G.; Zhou, Y. Q.; Boxer, L. M.; Woolley, F. R.; Zingaro, R. A. Artificial zinc(II) complexes regulate cell cycle and apoptosis-related genes in tumor cell lines. ChemBioChem 2007, 8, 332–340.
   PubMed Web of Science ®Google Scholar
• Hothi, H. S.; Makkar, A.; Sharma, J. R.; Manrao, M. R. Synthesis and antifungal potential of Co(II) complexes of 1-(2′-hydroxyphenyl)ethylideneanilines. Eur. J. Med. Chem. 2006, 41, 253–255.
   PubMed Web of Science ®Google Scholar
• Patil, M.; Hunoor, R.; Gudasi, K. Transition metal complexes of a new hexadentate macroacyclic N2O4-donor Schiff base: Inhibitory activity against bacteria and fungi. Eur. J. Med. Chem. 2010, 45, 2981–2986.
   PubMed Web of Science ®Google Scholar
• Tumer, M.; Ekinci, D.; Tumer, F.; Bulut, A. Synthesis, characterization and properties of some divalent metal(II) complexes: their electrochemical, catalytic, thermal and antimicrobial activity studies. Spectrochim. Acta A: Mol. Biomol. Spectrosc. 2007, 67, 916–929.
   PubMed Web of Science ®Google Scholar