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Cobalt(II) and Nickel(II) Complexes of Hydrazone Ligand ({(1E)-1-Aza-2-pyrrol-2-ylvinyl}{5,6-diphenyl(1,2,4-triazin-3-yl)}amine): Synthesis, Spectral, pH Metric, Antimicrobial and PM3 Studies
Corresponding Author(s) : Fatma Samy
Asian Journal of Chemistry,
Vol. 28 No. 12 (2016): Vol 28 Issue 12
Abstract
Binary and ternary complexes have been synthesized by reaction of the hydrazone ligand, (HL) with cobalt(II) nitrate and nickel(II) nitrate in absence and presence of second ligands. The new complexes have been characterized by elemental and thermal analyses, conductivity and magnetic susceptibility measurements as well as IR, UV-visible, ESR and mass spectra. The binary complexes have tetrahedral geometry, but ternary complexes have square planar, square pyramidal and octahedral geometries. The ligand acts as a monobasic tridentate and bidentate donor, for binary and ternary complexes, respectively. The pH metric studies at different temperature are used to calculate stepwise stability constants and thermodynamic parameters of Co(II) and Ni(II) complexes in 75 % (v/v) dioxane-water. The hyperchem 7.52 program utilized to determine the optimized structures of the ligand and its complexes. The correlation between theoretical and the experimental data of (IR and UV-visible) spectra of the complexes are good. The metal complexes exhibited remarkable antimicrobial activity.
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- N. Ozbek, S. Alyar, H. Alyar, E. Şahin and N. Karacan, Spectrochim. Acta A, 108, 123 (2013); doi:10.1016/j.saa.2013.01.005.
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- H.S. Seleem, A.A.T. Ramadan, A. Taha and F. Samy, Res. J. Chem. Sci., 1, 109 (2011).
- Hyperchem version 7.5 Hypercube Inc. (2003).
- A.W. Bauer, W.W.M. Kirby, J.C. Sherris and M. Turck, Am. J. Clin. Pathol., 45, 493 (1966).
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- A.B.P. Lever, Inorganic Electronic Spectroscopy, Elsevier, Amsterdam, edn 2 (1984).
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- A.W. Coats and J.P. Redfern, Nature, 201, 68 (1964); doi:10.1038/201068a0.
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References
N. Ozbek, S. Alyar, H. Alyar, E. Şahin and N. Karacan, Spectrochim. Acta A, 108, 123 (2013); doi:10.1016/j.saa.2013.01.005.
E.N. Nfor, A. Husian, F. Majoumo-Mbe, I.N. Njah, O.E. Offiong and S.A. Bourne, Polyhedron, 63, 207 (2013); doi:10.1016/j.poly.2013.07.028.
D.S. Raja, E. Ramachandran, N.S.P. Bhuvanesh and K. Natarajan, Eur. J. Med. Chem., 64, 148 (2013); doi:10.1016/j.ejmech.2013.03.040.
S.S. Machakanur, B.R. Patil, D.S. Badiger, R.P. Bakale, K.B. Gudasi and S.W. Annie Bligh, J. Mol. Struct., 1011, 121 (2012); doi:10.1016/j.molstruc.2011.12.023.
M. Krecmerova, M. Masojidkova and A. Holy, Bioorg. Med. Chem., 18, 387 (2010); doi:10.1016/j.bmc.2009.10.044.
M. Shebl, M.A. El-ghamry, S.M.E. Khalil and M.A.A. Kishk, Spectrochim. Acta A, 126, 232 (2014); doi:10.1016/j.saa.2014.02.014.
O.M.I. Adly and A.A.A. Emara, Spectrochim. Acta A, 132, 91 (2014); doi:10.1016/j.saa.2014.04.118.
B. Machura, A. Switlicka, R. Kruszynski, J. Mrozinski, J. Klak and J. Kusz, Polyhedron, 27, 2959 (2008); doi:10.1016/j.poly.2008.05.033.
H.S. Seleem, A.A.T. Ramadan, A. Taha and F. Samy, Res. J. Chem. Sci., 1, 109 (2011).
Hyperchem version 7.5 Hypercube Inc. (2003).
A.W. Bauer, W.W.M. Kirby, J.C. Sherris and M. Turck, Am. J. Clin. Pathol., 45, 493 (1966).
H.S. Seleem, A.A.T. Ramadan, A. Taha, M.F. Eid and F. Samy, Spectrochim. Acta A, 78, 1097 (2011); doi:10.1016/j.saa.2010.12.058.
S.A. Sallam, J. Coord. Chem., 60, 951 (2007); doi:10.1080/00958970600987990.
H.S. Seleem, G.A. El-Inany, B.A. El-Shetary and M.A. Mousa, Chem. Cent. J., 5, 2 (2011); doi:10.1186/1752-153X-5-2.
M. Ghosh, M. Layek, M. Fleck, R. Saha and D. Bandyopadhyay, Polyhedron, 85, 312 (2015); doi:10.1016/j.poly.2014.08.014.
M. Shebl, S.M.E. Khalil, A. Taha and M.A.N. Mahdi, Spectrochim. Acta A, 113, 356 (2013); doi:10.1016/j.saa.2013.04.131.
J. Devi and N. Batra, Spectrochim. Acta A, 135, 710 (2015); doi:10.1016/j.saa.2014.07.041.
K. Nakamoto, IR and Raman Spectra of Inorganic and Coordination Compounds, John Wiley & Sons, edn 5 (1997).
H.S. Seleem, A.A. Emara and M. Shebl, J. Coord. Chem., 58, 1003 (2005); doi:10.1080/00958970500066606.
A.A. El-Asmy and G.A.A. Al-Hazmi, Spectrochim. Acta A, 71, 1885 (2009); doi:10.1016/j.saa.2008.07.005.
M. Shebl, S.M.E. Khalil and F.S. Al-Gohani, J. Mol. Struct., 980, 78 (2010); doi:10.1016/j.molstruc.2010.06.040.
R. Atkins, G. Brewer, E. Kokot, G.M. Mockler and E. Sinn, Inorg. Chem., 24, 127 (1985); doi:10.1021/ic00196a003.
A.B.P. Lever, Inorganic Electronic Spectroscopy, Elsevier, Amsterdam, edn 2 (1984).
M.M. Hassanien, I.M. Gabr, M.H. Abdel-Rhman and A.A. El-Asmy, Spectrochim. Acta A, 71, 73 (2008); doi:10.1016/j.saa.2007.11.009.
A.W. Coats and J.P. Redfern, Nature, 201, 68 (1964); doi:10.1038/201068a0.
M. Shebl, Spectrochim. Acta A, 117, 127 (2014); doi:10.1016/j.saa.2013.07.107.
H.M. Irving and H.S. Rossotti, J. Chem. Soc., 2904 (1954); doi:10.1039/jr9540002904; (b) H.M. Irving, H.S. Rossotti, K. Taugbøl, H. Theorell and B. Thorell, Acta Chem. Scand., 10, 72 (1956); doi:10.3891/acta.chem.scand.10-0072.
T.A. Yousef, G.M. Abu El-Reash, O.A. El-Gammal and S.F. Ahmed, Polyhedron, 81, 749 (2014); doi:10.1016/j.poly.2014.07.035.
O.A. El-Gammal, G.M. Abu El-Reash and M.M. El-Gamil, Spectrochim. Acta A, 96, 444 (2012); doi:10.1016/j.saa.2012.05.046.
M.T. Beck, Chemistry of Complex Equilibria, Van Nostrand (1970).
V. Gutmanns, The Donor-Acceptor Approach to Molecular Interaction, Plenum Press, New York, London (1978).