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This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis of Mn(II), Co(II), Ni(II) and Cu(II) Complexes of Schiff's Base Ligand: Spectral Studies, Molecular Modelling and Fungicidal Screening
Corresponding Author(s) : Sulekh Chandra
Asian Journal of Chemistry,
Vol. 31 No. 2 (2019): Vol. 31 No. 2
Abstract
Mn(II), Co(II), Ni(II) and Cu(II) complexes with Schiff's base ligand, 3-(benzo[b]thiophen-2-yliminomethyl)-benzene-1,2-diol have been synthesized. All the complexes were characterized by elemental analysis, molar conductance measurements, NMR, mass, IR, EPR and electronic spectral studies. The geometry of complexes has been optimized by using Gaussian 09 W. The complexes were found to be non electrolytes. These complexes have general composition [M(L)2X2] [where L = Schiff′s base ligand, M = Mn(II), Co(II), Ni(II) and Cu(II) and X = Cl−, CH3COO−]. Spectral data indicates octahedral geometry for Mn(II), Co(II), Ni(II), but Cu(II) complexes were found to have tetragonal geometry. The fungal activity of ligand and complexes has been examined against fungi Aspergillus niger and Candida tropicalis by means of food poison method. The results suggest that the metal complexes show better antifungal activity in the comparison of ligand.
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G. Grivani, S. Delkhosh, K. Fejfarová, M. Dusek and A.D. Khalaji, Inorg. Chem. Commun., 27, 82 (2013); https://doi.org/10.1016/j.inoche.2012.10.029.
P. Souza, A. Josa, G. Vazquez and J.R. Masaguer, Transition Met. Chem., 10, 410 (1985); https://doi.org/10.1007/BF01096746.
C.J. Dhanraj and M.S. Nair, J. Coord. Chem., 62, 4018 (2009); https://doi.org/10.1080/00958970903191142.
S. Chandra and S. Gautam, Int. J. Chem. Pharm. Sci, 5, 27 (2014).
S. Rani, S. Kumar and S. Chandra, Spectrochim. Acta A Mol. Biomol. Spectrosc., 118, 244 (2014); https://doi.org/10.1016/j.saa.2013.08.079.
S. Chandra, S. Bargujar, R. Nirwal and N. Yadav, Spectrochim. Acta A Mol. Biomol. Spectrosc., 106, 91 (2013); https://doi.org/10.1016/j.saa.2012.12.014.
S. Di Bella and I. Fragala, New J. Chem., 26, 285 (2002); https://doi.org/10.1039/B108672C.
P.G. Cozzi, L.S. Dolci, A. Garelli, M. Montalti, L. Prodi and N. Zaccheroni, New J. Chem., 27, 692 (2003); https://doi.org/10.1039/b209396k.
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S. Karabocek, S. Guner and N. Karabocek, Inorg. Biochem., 66, 57 (1997); https://doi.org/10.1016/S0162-0134(96)00160-2.
P. Anand and V.M. Patil, V.K. Sharma, R.L. Khosa and N. Masand, Int. J. Drug Design Dicscov., 3, 851 (2012).
D. Bose, J. Banerjee, S.H. Rahaman, G. Mostafa, H.-K. Fun, R.D. Bailey Walsh, M.J. Zaworotko and B.K. Ghosh, Polyhedron, 23, 2045 (2004); https://doi.org/10.1016/j.poly.2004.04.035.
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M. Barwiolek, E. Szlyk, A. Surdykowski and A. Wojtczak, Dalton Trans., 42, 11476 (2013); https://doi.org/10.1039/c3dt50213a.
A.M. Alafeefy, Pharm. Biol., 46, 751 (2008); https://doi.org/10.1080/13880200802315907.
C.V. Yelamaggad, G. Shanker, U.S. Hiremath and S.K. Prasad, J. Mater. Chem., 18, 2927 (2008); https://doi.org/10.1039/b804579h.
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S. Chandra, D. Jain and Anupma, J. Ind. Chem. Soc., 87, 1245 (2010).
J. Joseph and G.B. Janaki, J. Mol. Struct., 1063, 160 (2014); https://doi.org/10.1016/j.molstruc.2014.01.028.
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S. Chandra and Ruchi, Spectrochim. Acta A Mol. Biomol. Spectrosc., 103, 338 (2013); https://doi.org/10.1016/j.saa.2012.10.065.
U. Kumar and S. Chandra, E. J. Coord. Chem., 7, 1238 (2010); https://doi.org/10.1155/2010/518723.
S. Chandra, S. Verma, U. Dev and N. Joshi, J. Coord. Chem., 74, 1327 (2009); https://doi.org/10.1080/00958970802521076.
H.D. Yin, M. Hong, Q.B. Wang, S.C. Xue and D.Q. Wang, J. Organomet Chem., 690, 1669 (2005); https://doi.org/10.1016/j.jorganchem.2004.12.037.
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S. Chandra, L.K. Gupta and Sangeetika, Synth. React. Inorg. Met.-Org. Chem., 34, 1591 (2004); https://doi.org/10.1081/SIM-200026596.
A.B.P. Lever, Crystal Field Spectra, Inorgoranic Electronic Spectroscopy, Elsevier: Amesterdam, edn 1, p. 249 (1984).
M. Sobiesiak, T. Muziol, M. Rozalski, U. Krajewska and E. Budzisz, New J. Chem., 38, 5349 (2014); https://doi.org/10.1039/C4NJ00977K.
B. Mohani and F. Arjmand, Bioinorg. Chem. Appl., 2, 225 (2004); https://doi.org/10.1155/S1565363304000147.
M. Shakir, A.K. Mohamed, S.P. Varkey, O.S.M. Nasman and Z.A. Siddiqi, Polyhedron, 14, 1277 (1995); https://doi.org/10.1016/0277-5387(94)00406-5.
B.J. Hathaway and D.E. Billing, Coord. Chem. Rev., 5, 143 (1970); https://doi.org/10.1016/S0010-8545(00)80135-6.
S. Chandra, V.P. Sangeetika, V.P. Tyagi and S. Raizada, Synth. React. Inorg. Met.-Org. Chem., 33, 147 (2003); https://doi.org/10.1081/SIM-120016879.
S. Chandra, L.K. Gupta and Sangeetika, Spectrochim. Acta A Mol. Biomol. Spectrosc., 62, 453 (2005); https://doi.org/10.1016/j.saa.2005.01.015.
B.K. Rai, V. Singh, P. Sinha, S.N. Vidyarthi, B. Sahi, A. Pandey and A. Amit, Orient. J. Chem., 30, 1411 (2014); https://doi.org/10.13005/ojc/300363.
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S. Chandra and L.K. Gupta, Transition Met. Chem., 30, 630 (2005); https://doi.org/10.1007/s11243-005-4826-4.
M. Tyagi, S. Chandra and P. Tyagi, Spectrochim. Acta Part A: Mol. Biomol. Spectrosc., 117, 1 (2014); https://doi.org/10.1016/j.saa.2013.07.074.
S. Belaid, A. Landreau, S. Djebbar, O. Benali-Baitich, G. Bouet and J.-P. Bouchara, J. Inorg. Biochem., 102, 63 (2008); https://doi.org/10.1016/j.jinorgbio.2007.07.001.