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Synthesis and Characterization of Neodymium(III) Ternary Complex Using Lansoprazole and Uracil as Ligands
Corresponding Author(s) : Sarika Verma
Asian Journal of Chemistry,
Vol. 28 No. 11 (2016): Vol 28 Issue 11
Abstract
Ternary complex of neodymium has been synthesized by reacting neodymium(III) nitrate hexahydrate with two different (dual) biochemical ligands. One of the ligand used is an antiulcer drug, lansoprazole, 2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)pyridine-2-yl]methyl]sulfinyl]-1H-benzimidazole, other is uracil which is a RNA bases. The complex was synthesized in ethanolic medium and refluxed in reaction medium in 1:1:1, M:L:L ratio. The percentage yield of synthesized neodymium complex was 93 %. The complex was purple coloured solid and of the type (Llanso.Nd.LUra.4H2O)X·nH2O, where X is NO42-. The synthesized complex was characterized by various complementary techniques namely elemental analysis, Fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy (1H NMR), ultra violet-visible spectroscopy, mass spectroscopy, X-ray diffraction, scanning electron microscopy. An IR spectrum indicates that all the ligands behave as bidentate ligand. Molar conductance studies indicate electrolytic behaviour of the complex. Free energy changes were also calculated of synthesized complex. The complex has been screened for their antibacterial activity towards Streptococus faecalis bacteria. The results revealed that the metal chelates showed more resistance as compared with parent drug.
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J. Kido and Y. Okamoto, Chem. Rev., 102, 2357 (2002); doi:10.1021/cr010448y.
P.K. Mang, S. Larochelle and M. Greven, Nature, 426, 139 (2003); doi:10.1038/426139b.
K. Kuriki, Y. Koike and Y. Okamoto, Chem. Rev., 102, 2347 (2002); doi:10.1021/cr010309g.
C. Benelli and D. Gatteschi, Chem. Rev., 102, 2369 (2002); doi:10.1021/cr010303r.
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S.J. Franklin, Curr. Opin. Chem. Biol., 5, 201 (2001); doi:10.1016/S1367-5931(00)00191-5.
M. Khorasani-Motlagh, M. Noroozifar, S. Niroomand and J. Saffari, J. Iran. Chem. Soc., 7, 807 (2010); doi:10.1007/BF03246072.
P.K. Irena, L.M. Ilia and K.R. Maritza, Acta Pharm., 54, 119 (2004).
A.L. El-Ansary and N.S. Abdel-Kader, Int. J. Inorg. Chem., Article ID 901415 (2012); doi:10.1155/2012/901415.
F. Liu, G.-Y. Lu, W.-J. He, Z.-S. Wang and L.-G. Zhu, Chin. J. Chem., 19, 317 (2001); doi:10.1002/cjoc.20010190321.
A. Kothari, R.K. Jain and S.N. Mishra, Proc. Ind. Natn. Sci. Acad., 49a, 398 (1983).
S.C. Sweetman, Martindale-The Complete Drug Reference, Pharmaceutical Press; London, edn 34, p. 1269 (2005).
Asian Edition, Rockville, United States Pharmacopeia Convention, Inc, p. 1110 (2005).
G.T. Keith, in ed.: A.R. Gennaro, Gastrointestinal and Liver Drugs, Remington: The Science and Practice of Pharmacy, Lippincott Williams and Wilkins, Maryland, USA, edn 20, Vol. I, p. 1226 (2000).
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O.P. Agarwal, Chemistry of Organic Natural Products, Krishan Prakashan, Meerut, India, vol. 2 (2010).
R.H. Garrett and C.M. Grisham, Principals of Biochemistry with a Human Focus, S. Chand (G/L) & Company Ltd., India (1997).
D.J. Brown, The Pyrimidines, Interscience Publishers, New York (1962).
H.R. Horton, Principles of Biochemistry, Upper Saddle River, Pearson Prentice Hall, NJ (2006).
R.M. Silverstein, F.X. Webster and D.J. Kiemle, Spectrophotometric Identification of Organic Compounds, John Wiley, New York, edn 7 (2005).
J.R. Dyer, Application of Absorption Spectroscopy of Organic Compounds, Prentice Hall of India Pvt. Ltd., New Delhi (2011).
K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds, John Wiley & Sons, New York, edn 4, p. 208 (1993).
A.R. Sarkar and S. Mandal, Met. Based Drugs, 7, 157 (2000); doi:10.1155/MBD.2000.157.
P. Erno, B. Philippe and B. Martin, NMR Structure Determination of Organic Compounds, Springer-Verlag Berlin, Heidelberg (2009).
S.P. Sinha, J. Inorg. Nucl. Chem., 33, 2205 (1971); doi:10.1016/0022-1902(71)80582-1.
M. Mohan, J.P. Tandon and N.S. Gupta, Inorg. Chim. Acta, 111, 187 (1986);
doi:10.1016/S0020-1693(00)84650-2.
Powder Diffraction File, Alphabetical Index Inorganic Phases, Published By JCPDS International Centre for Diffraction Data 1601, Park Lane Swarthmore, Pennsylvania 19081 USA (1984).
F.W. McLafferty and F.K. Tureek, Interpretation of Mass Spectra Hardcover, May 1 (1993).
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