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Complexes of Pyrimidine Thiones: Mechanochemical Synthesis and Biological Evaluation
Corresponding Author(s) : Pooja Sethi
Asian Journal of Chemistry,
Vol. 32 No. 10 (2020): Vol 32 Issue 10
Abstract
A new series of metal complexes with 1-(2-methylphenyl)-4,4,6-trimethyl pyrimidine-2-thione (2-HL1) and 1-(4-methylphenyl)-4,4,6-trimethyl pyrimidine-2-thione (4-HL2) ligands, [M(mppt)2(H2O)n] (M(II) = Cu, Mn, Co; n = 2 and M(II) = Ni, Zn; n = 0) have been synthesized using mechanochemical protocol. The complexes have been framed as [M(mppt)2(H2O)n] due to 1:2 (metal:ligand) nature of these metal complexs. Structures have been further confirmed on the basis of elemental analysis, Magnetic susceptibility measurements, electronic, infrared, far infrared, proton NMR, Mass spectral moment and thermogravimetric analysis studies. The infrared spectral data suggested that ligand behaves as a bidentate, coordinating through – N (endocyclic) and – S (exocyclic) donor atoms. All the compounds have also been screened for antibacterial and DNA photocleavage potential. Ligands complexed with Mn and Ni metals have shown the effect of substitution on their biological potentials. It was found that substitution at 4th or para position makes the ligand and its metal complexes have better antibacterial and DNA photocleaving agents.
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E.S. Raper, Coord. Chem. Rev., 153, 199 (1996); https://doi.org/10.1016/0010-8545(95)01233-8
V. Sharma, N. Chitranshi and A.K. Agarwal, Int. J. Med. Chem., 2014, 202784 (2014); https://doi.org/10.1155/2014/202784
K.L. Haas and K.J. Franz, Chem. Rev., 109, 4921 (2009); https://doi.org/10.1021/cr900134a
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T.S. Lobana, R. Sharma, G. Bawa and S. Khanna, Coord. Chem. Rev., 253, 977 (2009); https://doi.org/10.1016/j.ccr.2008.07.004
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J.R. Anacona, E. Bastardo and J. Camus, Transition. Met. Chem., 24, 478 (1999); https://doi.org/10.1023/A:1006997706762
J. Lewis and R.G. Wilkins, Modern Coordination Chemistry, Interscience: New York (1967).
M. Gulcan and M. Sonmez, Phosphorus Sulfur Silicon Rel. Elem., 186, 1962 (2011); https://doi.org/10.1080/10426507.2011.553501
B.N. Figgis, J. Lewis and F.A. Cotton, ed.: F.A. Cotton, Progress in Inorganic Chemistry, Interscience: New York (1964).
E.N. Sathyanarayana, Electronic Absorption Spectroscopy and Related Techniques, University Press: India (2001).
B.E. Douglas, D.H. McDaniel and J.J. Alexander, Concepts and Models of Inorganic Chemistry, Wiley: New York, edn 3 (1994).
L. Casella and M. Gullotti, J. Am. Chem. Soc., 103, 6338 (1981); https://doi.org/10.1021/ja00411a013
A.A. Osowole, R. Kempe, R. Schobert and K. Effenberger, Synth. React. Inorg. Met. Org. Chem. Nano-Met. Chem., 41, 825 (2011); https://doi.org/10.1080/15533174.2011.591310
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Z.H. Chohan, A. Scozzafava and C.T. Supuran, J. Enzyme Inhib. Med. Chem., 18, 259 (2003); https://doi.org/10.1080/1475636031000071817
U.M. Hassan, C.T. Chohan and C.T. Supuran, Main Group Met. Chem., 25, 291 (2002); https://doi.org/10.1515/MGMC.2002.25.5.291
Z.H. El-Wahab, M.M. Mashaly, A.A. Salman, B.A. El-Shetary and A.A. Faheim, Spectrochim. Acta A Mol. Biomol. Spectrosc., 60, 2861 (2004); https://doi.org/10.1016/j.saa.2004.01.021
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