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Synthesis, Characterization and Antimicrobial Studies of Novel Binuclear Transition Metal Complexes of Schiff Base Derived from 1-Amino-5-methyl-2,6-pyrimidine-dione and 2,3-Butanedione
Corresponding Author(s) : Netra Pal Singh
Asian Journal of Chemistry,
Vol. 25 No. 1 (2013): Vol 25 Issue 1
Abstract
A series of binuclear transition metal complexes of the type [M2(L)2X4)]·nH2O (where, M = Cu(II), Ni(II), Co(II) or Zn(II), X= Cl–/CH3COO– and L = ligand) of a Schiff base ligand derived from 1-amino-5-methyl-2,6-pyrimidine-dione and 2,3-butanedione have been synthesized and characterized by elemental analysis, molar conductance measurements, magnetic moment measurements, IR, UV-visible, 1H NMR, EPR and mass spectral studies. Electronic spectral data and magnetic moment values indicate octahedral geometry for all the metal complexes. In vitro antimicrobial activity of ligand and its metal complexes were also studied against bacteria (Bacillus subtilis and Escherichia coli) and fungi (Aspergillus niger and Aspergillus flavus) which show antimicrobial activity of ligand and binuclear metal complexes.
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- J.A.R. Navarro and B. Lippert, Coord. Chem. Rev., 222, 219 (2001).
- M. Sonmez, M. Celebi and I. Berber, Eur. J. Med. Chem., 4, 1935 (2010).
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- E. Colacio, J.M. Dominguez-Vera, A. Romerosa, R. Kivekas, M. klinga and A. Escuer, Inorg. Chim. Acta, 234, 61 (1995).
- M.S. Masoud, E.A. Khalil,A.M. Hindawy, A.E. Ali and E.F. Mohamed, Spectrochim. Acta A, 60, 2807 (2004).
- M.D. Revenco, O.V. Palamarciuc, P.N. Bourosh, J. Lipkowski, M. Gdaniec, Y.A. Simonov and R. Clerac, Inorg. Chim. Acta, 368, 157 (2011).
- S. Tabassum, G.C. Sharma, F. Arjmand and A. Azam, Nanotechnology, 21, 195102 (2010).
- N.P. Singh and A.N. Srivastava, E-J. Chem., 8, 809 (2010).
- K. Kohda, I. Kobayashi, K. Itano, S. Asano and Y. Kawazoe, Tetrahedron, 49, 3947 (1993).
- C.N. Reilley, R.W. Schmidt and F.A. Sadek, J. Chem. Educ., 36, 619 (1959).
- A.I. Vogel,A Text Book of Quantitative Inorganic Analysis, Longmans, London, p. 433 (1961).
- A.K. Sadna, Y. Mirza, A. R. Aneja and O. Prakash, Eur. J. Med. Chem., 38, 533 (2003).
- W.J. Geary, Coord. Chem. Rev., 7, 81 (1971).
- M. Dolze, M. Tumer and M. Digrak, Transition Met. Chem., 29, 516 (2004).
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- A. Alagha, L. Parthasrathi, D. Gaynor, H.M. Bunz, Z.A. Starikova, E. Farkas, E.C.O. Brien, M.J. Gil and K.B. Nolan, Inorg. Chim. Acta, 368, 58 (2011).
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- M. Sonmez and M. Sekerci, Polish J. Chem., 76, 907 (2002).
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- R.M. Silverstein, C.M. Bassler and T.C. Morrill, Spectrometric Identification of Organic Compounds, New York: John Wiley, edn. 3 (1974).
- G. Ferguson, J.N. Low, M. Quiros-Olozabal, J.M. Salas-Peregrin, F. Hueso-Urena and M.N. Moreno-Carretero, Polyhedron, 15, 3233 (1996).
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- G.G. Mohamed, M.A. Zayed and N.E.A. El-Gamel, Spectrochim. Acta A, 58, 3167 (2002).
- A.M. Herrera, R.J. Staples, S.V. Kryotov, A.Y. Nazarenko and E. Vakimova, J. Chem. Soc. Dalton Trans., 846 (2003).
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- A. Bansal, S. Kumar and R.V. Singh, Synth. React. Inorg. Met. Org. Chem., 31, 1085 (2001).
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References
J.A.R. Navarro and B. Lippert, Coord. Chem. Rev., 222, 219 (2001).
M. Sonmez, M. Celebi and I. Berber, Eur. J. Med. Chem., 4, 1935 (2010).
S.E.M. Khali, H.S. Saleem, B.A. El-Shetary and M. Shebl, J. Coord. Chem., 55, 883 (2002).
T.F. Mastropietro, D. Armentano, E. Grisolia, C. Zanchini, F. Lloret, M. Julve and G.D. Munno, J. Chem. Soc. Dalton Trans., 514 (2008).
E. Colacio, J.M. Dominguez-Vera, A. Romerosa, R. Kivekas, M. klinga and A. Escuer, Inorg. Chim. Acta, 234, 61 (1995).
M.S. Masoud, E.A. Khalil,A.M. Hindawy, A.E. Ali and E.F. Mohamed, Spectrochim. Acta A, 60, 2807 (2004).
M.D. Revenco, O.V. Palamarciuc, P.N. Bourosh, J. Lipkowski, M. Gdaniec, Y.A. Simonov and R. Clerac, Inorg. Chim. Acta, 368, 157 (2011).
S. Tabassum, G.C. Sharma, F. Arjmand and A. Azam, Nanotechnology, 21, 195102 (2010).
N.P. Singh and A.N. Srivastava, E-J. Chem., 8, 809 (2010).
K. Kohda, I. Kobayashi, K. Itano, S. Asano and Y. Kawazoe, Tetrahedron, 49, 3947 (1993).
C.N. Reilley, R.W. Schmidt and F.A. Sadek, J. Chem. Educ., 36, 619 (1959).
A.I. Vogel,A Text Book of Quantitative Inorganic Analysis, Longmans, London, p. 433 (1961).
A.K. Sadna, Y. Mirza, A. R. Aneja and O. Prakash, Eur. J. Med. Chem., 38, 533 (2003).
W.J. Geary, Coord. Chem. Rev., 7, 81 (1971).
M. Dolze, M. Tumer and M. Digrak, Transition Met. Chem., 29, 516 (2004).
M.S. Masoud, E.A. Khalil, A.M. Hindway, A.E. Ali and E.F. Mohmed, Spectrochim. Acta A, 60, 2807 (2004).
A. Alagha, L. Parthasrathi, D. Gaynor, H.M. Bunz, Z.A. Starikova, E. Farkas, E.C.O. Brien, M.J. Gil and K.B. Nolan, Inorg. Chim. Acta, 368, 58 (2011).
K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds, Wiley, New York (1986).
R.C. Maurya, J. Chourasia and P. Sharma, Indian J. Chem., 47A, 517 (2008).
L.J. Bellamy, The Infrared Spectra of Complex Molecules, Chapmann and Hall, London (1978).
M. Sonmez and M. Sekerci, Polish J. Chem., 76, 907 (2002).
G. Kumar, D. Kumar, S. Devi, R. Johri and C.P. Singh, Eur. J. Med. Chem., 45, 3056 (2010).
R.M. Silverstein, C.M. Bassler and T.C. Morrill, Spectrometric Identification of Organic Compounds, New York: John Wiley, edn. 3 (1974).
G. Ferguson, J.N. Low, M. Quiros-Olozabal, J.M. Salas-Peregrin, F. Hueso-Urena and M.N. Moreno-Carretero, Polyhedron, 15, 3233 (1996).
A.B.P. Lever, Inorganic Electronic Spectroscopy, Elsevier, New York, edn. 2 (1968).
G.G. Mohamed, M.A. Zayed and N.E.A. El-Gamel, Spectrochim. Acta A, 58, 3167 (2002).
A.M. Herrera, R.J. Staples, S.V. Kryotov, A.Y. Nazarenko and E. Vakimova, J. Chem. Soc. Dalton Trans., 846 (2003).
D.R. Lorenz, J.R. Wasson, D.K. Johonson and D.A. Thorpe, J. Inorg. Nucl. Chem., 37, 2297 (1975).
A. Bansal, S. Kumar and R.V. Singh, Synth. React. Inorg. Met. Org. Chem., 31, 1085 (2001).
N. Dharmaraj, P. Viswanathamurthi, K. Natarajan, Transition Met. Chem., 26, 105 (2002)