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Synthesis and Thermogravimetric Behaviour of Ni(II), Cu(II) and Zn(II) Complexes of Triazine-Salicyldamine Schiff Bases
Corresponding Author(s) : Abdulaziz Ali Alomari
Asian Journal of Chemistry,
Vol. 27 No. 11 (2015): Vol 27 Issue 11
Abstract
Synthesis, characterization and thermogravimetric behaviour of Ni(II), Cu(II) and Zn(II) complexes of Schiff bases derived from 4-phenyl-1,3,5-triazine-2,6-diamine and 5-chloro- salicylaldehyde (H2L1), 5-bromo-salicylaldehyde (H2L2) have been reported. The ligands were characterized by FT-IR, 1H and 13C NMR, UV-visible spectroscopy as well as elemental analysis. Spectral studies revealed that the ligands were acting as tetradentate chelating agents and coordinated to the metal center via deprotonated phenolate oxygen and azomethine nitrogen atoms in a 1:1 ligand to metal ratio. Thermal behaviour of the complexes has been evaluated using TGA. All complexes showed similar modes of three steps weight loss upon heating to 800 °C with gradual loss of organic and inorganic parts. The residues after heating corresponds to metal oxides, with copper complexes seemed to be the most stable and can be used in high-temperature catalytic cycles.
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- G. Ceyhan, M. Köse, M. Tümer, I. Demirtaş, A.Ş. Yaglioglu and V. McKee, J. Lumin., 143, 623 (2013); doi:10.1016/j.jlumin.2013.06.002.
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References
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(a) A. Gölcü, M. Tümer, H. Demirelli and R.A. Wheatley, Inorg. Chim. Acta, 358, 1785 (2005); doi:10.1016/j.ica.2004.11.026; (b) M. Dolaz and M. Tümer, Transition Met. Chem., 29, 516 (2004); doi:10.1023/B:TMCH.0000037518.92549.49.
T.P. Yoon and E.N. Jacobsen, Science, 299, 1691 (2003); doi:10.1126/science.1083622.
S.A. Abdel-Latif, H.B. Hassib and Y.M. Issa, Spectrochim. Acta A, 67, 950 (2007); doi:10.1016/j.saa.2006.09.013.
B. Tang, X. Sun, G. Liu and H. Li, J. Mol. Struct., 984, 111 (2010); doi:10.1016/j.molstruc.2010.09.014.
C. Maxim, T.D. Pasatoiu, V.C. Kravtsov, S. Shova, C.A. Muryn, R.E.P. Winpenny, F. Tuna and M. Andruh, Inorg. Chim. Acta, 361, 3903 (2008); doi:10.1016/j.ica.2008.03.013.
Y. Sunatsuki, Y. Motoda and N. Matsumoto, Coord. Chem. Rev., 226, 199 (2002); doi:10.1016/S0010-8545(01)00417-9.
R. Ziessel, Coord. Chem. Rev., 216–217, 195 (2001); doi:10.1016/S0010-8545(00)00410-0.
S. Yamada, Coord. Chem. Rev., 190–192, 537 (1999); doi:10.1016/S0010-8545(99)00099-5.
S. Selvamurugan, P. Viswanathamurthi, A. Endo, T. Hashimoto and K. Natarajan, J. Coord. Chem., 66, 4052 (2013); doi:10.1080/00958972.2013.858135.
E. Kimura, S. Wada, M. Shionoya and Y. Okazaki, Inorg. Chem., 33, 770 (1994); doi:10.1021/ic00082a025.
S.L. Lambert, C. Spiro, R.R. Gagne and D.N. Hendrickson, Inorg. Chem., 21, 68 (1982); doi:10.1021/ic00131a013.
K.C. Gupta and A.K. Sutar, Coord. Chem. Rev., 252, 1420 (2008); doi:10.1016/j.ccr.2007.09.005.
K. Singh, M.S. Barwa and P. Tyagi, Eur. J. Med. Chem., 42, 394 (2007); doi:10.1016/j.ejmech.2006.10.016.
Z.H. Chohan, H. Pervez, A. Rauf, K.M. Khan, G.M. Maharvi and C.T. Supuran, J. Enzyme Inhib. Med. Chem., 19, 161 (2004); doi:10.1080/14756360310001656745.
M. Mashaly, H.A. Bayoumi and A. Taha, Chem. Papers Chem. Zvesti., 53, 299 (1999).
L.C. Felton and J.H. Brewer, Science, 105, 409 (1947); doi:10.1126/science.105.2729.409.
A. Ali, N. Abdullah, M.J. Maah and M.M. Ibrahim, Asian J. Chem., 24, 5063 (2012).
S. Zolezzi, A. Decinti and E. Spodine, Polyhedron, 18, 897 (1999); doi:10.1016/S0277-5387(98)00376-3.
L. Sacconi, Coord. Chem. Rev., 1, 126 (1966); doi:10.1016/S0010-8545(00)80165-4.
L.J. Bellamg, The Infrared Spectra of Complex molecules, Chapman and Hall, London (1975).
M.G. Martin Reyes, P. Gili, P. Martin Zarza, A. Medina Ortega and M.C. Diaz Gonzales, Inorg. Chim. Acta, 116, 153 (1986); doi:10.1016/S0020-1693(00)82168-4.
G.C. Percy, J. Inorg. Nucl. Chem., 37, 2071 (1975); doi:10.1016/0022-1902(75)80832-3.
D.M. Adams, Metal ligand and Related Vibrations, Edward Arnold, London, pp. 248-284 (1967).
Z.-L. Yuan, Q.-L. Zhang, X. Liang, B.-X. Zhu, L.F. Lindoy and G. Wei, Polyhedron, 27, 344 (2008); doi:10.1016/j.poly.2007.09.012.
P. Gili, P.M. Zarza, P. Núñez, A. Medina, M.C. Díaz, M.G. Martín, J.M. Arrieta, M. Vlassi, G. Germain, M. Vermeire and L. Dupont, J. Coord. Chem., 20, 273 (1989); doi:10.1080/00958978909408169.
A. Ray, D. Sadhukhan, G.M. Rosair, C.J. Gómez-García and S. Mitra, Polyhedron, 28, 3542 (2009); doi:10.1016/j.poly.2009.07.017.
S. Zolezzi, A. Decinti and E. Spodine, Polyhedron, 18, 897 (1999); doi:10.1016/S0277-5387(98)00376-3.
D. Nicholls, Complexes and First-Row Transition Elements, American Elsevier, New York (1975).
G. Ceyhan, C. Celik, S. Urus, I. Demirtas, M. Elmastas and M. Tumer, Spectrochim. Acta A, 81, 184 (2011); doi:10.1016/j.saa.2011.05.106.
E. Suresh, M.M. Bhadbhade and D. Srinivas, Polyhedron, 15, 4133 (1996); doi:10.1016/0277-5387(96)00178-7.
A. Çukurovali, I. Yilmaz, H. Özmen and M. Ahmedzade, Transition Met. Chem., 27, 171 (2002); doi:10.1023/A:1013913027732.
M. Tumer, D. Ekinci, F. Tumer and A. Bulut, Spectrochim. Acta A, 67, 916 (2007); doi:10.1016/j.saa.2006.09.009.