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Synthesis, Characterization and Antimicrobial Screening of Novel Hydrazide Ligand & It’s Transition Metal Complexes
Asian Journal of Chemistry,
Vol. 31 No. 4 (2019): Vol 31 Issue 4
Abstract
Different transition metal complexes were synthesized from novel 3-bromo-2-[1-(4-hydroxy-6-methyl- 2-oxo-2H-pyran-3-yl)ethylidene]hydrazide ligand (H2L) and characterized by spectral techniques. The synthesized ligand was found to act mono as well as di deprotonated (OH, NH) manner and stoichiometry of the ligand to metal ions was confirmed to be 1:1 in case of complex using metal chloride salts, whereas 1:2 in case of metal(II) complexes using metal acetate(II) salt. Structures of metal complexes were confirmed by IR, 1H NMR, TGA, XRD, elemental analysis and UV technique which revealed that Mn(II), Co(II), Ni(II), Cu(II) complexes were octahedral geometry and those of Cu(II), Zn(II) showed square planner and tetrahedral geometry around metal ion respectively. Furthermore H2L and its metal complexes were screened for antimicrobial activity which showed that ligand enhanced its biological activity after coordination with metal ions. In particular, Cd(II) and Mn(II) complexes exhibited excellent antifungal activity.
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- S. Naskar, S. Naskar, R.J. Butcher and S.K. Chattopadhyay, Inorg. Chim. Acta, 363, 404 (2010); https://doi.org/10.1016/j.ica.2009.11.007.
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- H.G. Aslan, S. Ozcan and N. Karacan, Inorg. Chem. Commun., 14, 1550 (2011); https://doi.org/10.1016/j.inoche.2011.05.024.
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- S.N. Pandeya, D. Sriram, G. Nath and E. DeClercq, Eur. J. Pharm. Sci., 9, 25 (1999); https://doi.org/10.1016/S0928-0987(99)00038-X.
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References
S. Naskar, S. Naskar, R.J. Butcher and S.K. Chattopadhyay, Inorg. Chim. Acta, 363, 404 (2010); https://doi.org/10.1016/j.ica.2009.11.007.
M.V. Angelusiu, S.F. Barbuceanu, C. Draghici and G.L. Almajan, Eur. J. Med. Chem., 45, 2055 (2010); https://doi.org/10.1016/j.ejmech.2010.01.033.
Q. Wang, Z.Y. Yang, G.F. Qi and D.-D. Qin, Biometals, 22, 927 (2009); https://doi.org/10.1007/s10534-009-9245-0.
H.G. Aslan, S. Ozcan and N. Karacan, Inorg. Chem. Commun., 14, 1550 (2011); https://doi.org/10.1016/j.inoche.2011.05.024.
V.P. Singh, A. Katiyar and S. Singh, Biometals, 21, 491 (2008); https://doi.org/10.1007/s10534-008-9136-9.
S.N. Pandeya, D. Sriram, G. Nath and E. DeClercq, Eur. J. Pharm. Sci., 9, 25 (1999); https://doi.org/10.1016/S0928-0987(99)00038-X.
S.A. Patil, M. Manjunath, U.V. Kamble and P.S. Badami, Der Pharma Chem., 3, 97 (2011).
E.W. Ainscough, A.M. Brodie, A.J. Dobbs, J.D. Ranford and J.M. Waters, Inorg. Chim. Acta, 267, 27 (1998); https://doi.org/10.1016/S0020-1693(97)05548-5.
A.A. Osowole, I. Ott and O.M. Ogunlana, Int. J. Inorg. Chem., Article 2012, ID 206417 (2012); https://doi.org/10.1155/2012/206417.
G. Marpadga, G.S. Rajender Reddy and M.C. Ganorkar, Transition Met. Chem., 21, 101 (1996); https://doi.org/10.1007/BF00136536.
S.M. Jadhav, A.S. Munde, S.G. Shankarwar, V.R. Patharkar, V.A. Shelke and T.K. Chondhekar, J. Korean Chem. Soc., 54, 515 (2010); https://doi.org/10.5012/jkcs.2010.54.5.515.
A. Ourari, W. Derafa and D. Aggoun, RSC Adv., 5, 82894 (2015); https://doi.org/10.1039/C5RA10819E.
Y. Nakayama, H. Bando, Y. Sonobe and T. Fujita, J. Mol. Catal. Chem., 213, 141 (2004); https://doi.org/10.1016/j.molcata.2003.11.025.
H.H. Monfared, S. Sadighian, M.A. Kamyabi and P. Mayer, J. Mol. Catal. Chem., 304, 139 (2009); https://doi.org/10.1016/j.molcata.2009.02.004.
K.G. Thomas and P.V. Kamat, J. Am. Chem. Soc., 122, 2655 (2000); https://doi.org/10.1021/ja9941835.
D.P. Singh, D.S. Raghuvanshi, K.N. Singh and V.P. Singh, J. Mol. Catal. A, 379, 21 (2013); https://doi.org/10.1016/j.molcata.2013.07.011.
S.S. Pawar, C.S. Patil, V.B. Tadke and R.P. Pawar, Int. J. Curr. Adv. Res., 7, 12934 (2018).
R.U. Ambhure, S.R. Mirgane, D.U. Thombal, R.B. Nawale, R.P. Marathe and R.P. Pawar, Modern Org. Chem. Res., 2, 11 (2017); https://doi.org/10.22606/mocr.2017.21003.
D.U. Thombal, S.R. Mirgane, R.U. Ambhure, R.P. Pawar and K.L. Ameta, Biochem. Biophys., 3, 7 (2017); https://doi.org/10.14355/bab.2017.03.002.
A.I. Vogel, Text Book of Practical Organic Chemistry, Longman: London, edn 5 (1989).
N. Chitrapriya, T. Sathiya Kamatchi, M. Zeller, H. Lee and K. Natarajan, Spectrochim. Acta A, 81, 128 (2011); https://doi.org/10.1016/j.saa.2011.05.069.
U. Kendur, G.H. Chimmalagi, S.M. Patil, K.B. Gudasi, C.S. Frampton, C.V. Mangannavar and I.S. Muchchandi, J. Mol. Struct., 1153, 299 (2018); https://doi.org/10.1016/j.molstruc.2017.10.022.
V. Kamat, D. Kokare, K. Naik, A. Kotian, S. Naveen, S.R. Dixit, N.K. Lokanath, S.D. Joshi and V.K. Revankar, Polyhedron, 127, 225 (2017); https://doi.org/10.1016/j.poly.2017.02.010.