Copyright (c) 2018 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Chelating Behaviour of Multidentate Ligand With Some Transition Metal(II) Ions
Corresponding Author(s) : Shivadhar Sharma
Asian Journal of Chemistry,
Vol. 30 No. 11 (2018): Vol 30 Issue 11
Abstract
A multidentate ligand, 1-benzoyl-2-(2′-carboxylphenyl)iminopropane (BIPH) has been prepared by the condensation of 1-phenylbutane-1,3-dione and anthranilic acid. This ligand has been used for chelation with Co(II), Ni(II) and Zn(II) metal ions as primary ligand while H2O, pyridine and α-picoline as the secondary ligands. The low value of molar conductivity of 10-3 M DMF solution of complexes shows that all the complexes are non-electrolyte. The comparison of IR spectra of complexes with that of free ligand reveals that the ligand chelates through deprotonated enolic -OH group oxygen and azomethine nitrogen and not through azomethine nitrogen and carboxylic oxygen or through carbonyl oxygen and carboxylic oxygen. On the basis of magnetic moment values and electronic spectra, octahedral symmetry has been assigned to these complexes with tetragonal distortion. Thermogravimetric analysis also confirms the tetragonal distortion with elongation along z-axis in complexes.
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S.J.S. Flora and V. Pachauri, Int. J. Environ. Res. Public Health, 7, 2745 (2010); https://doi.org/10.3390/ijerph7072745.
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H. Sigel and B. Martin, Chem. Rev., 82, 385 (1982); https://doi.org/10.1021/cr00050a003.
J.E. Coleman and D.P. Giedroc, Met. Ions Biol. Syst., 25, 171 (1979).
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P.B. Chakrawarty and R. Agarwal, Orient. J. Chem., 10, 119 (1994).
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M.A. Hitchman, Inorg. Chem., 11, 2387 (1972); https://doi.org/10.1021/ic50116a019.
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A. Joseph, B. Joseph and B. Narayana, J. Indian Chem. Soc., 85, 479 (2008).
I.P. Khullar and U. Agarwal, Can. J. Chem., 53, 1165 (1975); https://doi.org/10.1139/v75-161.
D. Kumar, J. Kumar, S. Chadha and S. Shymal, J. Indian Chem. Soc., 91, 185 (2014).
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A. Rastogi and A.K. Anurag Pandey, J. Indian Chem. Soc., 87, 1053 (2010).
R.L. Carlin and E. Weissberger, Inorg. Chem., 3, 611 (1964); https://doi.org/10.1021/ic50014a044.
A.B.P. Lever, I.M. Walker and P.J. McCarthy, Spectrosc. Lett., 12, 739 (1979); https://doi.org/10.1080/00387017908069200.
R. Ranjan, S. Suraiya, V. Kumar and S. Sharma, Proceedings of DAEBRNS, International Symposium on Material Chemistry, BARC, Mumbai, pp. 494-497 (2006).
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N.H. Butters, S.M. Mohaned, A.A. Sabah and E.A. Abdalarazaq, Asian J. Chem., 25, 4856 (2013); https://doi.org/10.14233/ajchem.2013.14125.
B. Krishnan and S.A. Iqbal, J. Indian Chem. Soc., 91, 367 (2014).
S. Karim and S. Saffrian, J. Indian Chem. Soc., 92, 325 (2015).
A.V. Nikolayev, V.A. Logvineko and L.I. Mychina, Thermal Analysis, Academic Press: New York, vol. 2, p. 779 (1969).