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Spectral and Biological Studies: Co(II), Ni(II), Cu(II), Zn(II) and Pd(II) Complexes of 5-Methyl-4-{(3-fluoro-4-methoxybenzylidiene)amino}-3-thiol-1,2,4-triazole
Corresponding Author(s) : Kiran Singh
Asian Journal of Chemistry,
Vol. 32 No. 12 (2020): Vol 32 Issue 12, 2020
Abstract
A series of metal-complexes of Co2+, Ni2+, Cu2+, Zn2+ and Pd2+ with new Schiff base named 5-methyl-4-((3-fluoro-4-methoxybenzylidiene)-amino)-3-thiol-s-triazole have been synthesized and characterized. Schiff base is formed by the condensation of 3-fluoro-4-methoxy-benzaldehyde and 4-amino-3-mercapto-5-methyl-1,2,4-triazoles (AMMT). After synthesis, Schiff base is characterized by IR and NMR techniques. Metal complexes are characterized by different techniques as IR, NMR, ESR, electronic and fluorescence. Elemental analysis and magnetic measurements of metal complexes have also been carried out. Using different techniques, tentative geometry for newly synthesized complexes have been proposed i.e. square planar for copper and palladium complexes and octahedral for rest of the metal complexes. The biological activities of all the metal complexes of this series are also examined.
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- R. Nazari, H. Golchoubian and G. Bruno, J. Iran. Chem. Soc., 16, 1041 (2019); https://doi.org/10.1007/s13738-018-01577-z
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- A.M. Khedr and H.M. Marwani, Int. J. Electrochem., 7, 10074 (2012).
- F.A. Cotton, C. Wilkinson and C.A. Murillo, Advanced Inorganic Chemistry, Wiley, New York, edn 6 (1999).
- A.K. Patra, S. Dhar, M. Nethaji and A.R. Chakravarty, Dalton Trans., 5, 896 (2005); https://doi.org/10.1039/b416711b
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- G.S. Kurdekar, S. Mudigoudar Puttanagouda, N.V. Kulkarni, S. Budagumpi and V.K. Revankar, Med. Chem. Res., 20, 421 (2011); https://doi.org/10.1007/s00044-010-9330-5
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References
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G.B. Bagihalli, S.A. Patil and P.S. Badami, J. Iran. Chem. Soc., 6, 259 (2009); https://doi.org/10.1007/BF03245833
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N.G. Kandile, M.I. Mohamed and H.M. Ismaeel, J. Enzyme Inhib. Med. Chem., 32, 119 (2017); https://doi.org/10.1080/14756366.2016.1238365
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Z.L. You, H.L. Zhu and W.S. Liu, J. Inorg. Gen. Chem., 630, 1617 (2004); https://doi.org/10.1002/zaac.200400125
K. Singh, M.S. Barwa and P. Tyagi, Eur. J. Med. Chem., 41, 147 (2006); https://doi.org/10.1016/j.ejmech.2005.06.006
S. Bala, R.P. Gupta, M.L. Sachdeva, A. Singh and H.K. Pujari, Indian J. Chem., 9, 481 (1978).
K.R. Aneja, C. Sharma and R. Joshi, Jundishapur J. Microbiol., 4, 175 (2011).
K. Singh, D.P. Singh, M.S. Barwa and P. Tyagi, J. Enzyme Inhib. Med. Chem., 21, 557 (2006); https://doi.org/10.1080/14756360600642131
P. Jayaseelan, S. Prasad, S. Vedanayaki and R. Rajavel, Arab. J. Chem., 9, S668 (2016); https://doi.org/10.1016/j.arabjc.2011.07.029
K. Singh, Y. Kumar, P. Puri, C. Sharma and K. Aneja, Med. Chem. Res., 21, 1708 (2012); https://doi.org/10.1007/s00044-011-9683-4
A.K. Mapari and K.V. Mangaonkar, Int. J. Chemtech Res., 3, 477 (2011).
K. Singh, Ritu and V. Kumar, Int. J. Inorg. Chem., 4, 32 (2014).
L.J. Fan and W.E. Jones, J. Phys. Chem. B, 110, 7777 (2006); https://doi.org/10.1021/jp056381q
N. Chattopadhyay, A. Mallick and S. Sengupta, J. Photochem. Photobiol. Chem., 177, 55 (2006); https://doi.org/10.1016/j.jphotochem.2005.05.011
D. Das, B. Chand, K. Sarker, J. Dinda and C. Sinha, Polyhedron, 25, 2333 (2006); https://doi.org/10.1016/j.poly.2006.01.033
G. Hennrich, H. Sonnenschein and U. Resch-Genger, J. Am. Chem. Soc., 121, 5073 (1999); https://doi.org/10.1021/ja983802r
R. Nazari, H. Golchoubian and G. Bruno, J. Iran. Chem. Soc., 16, 1041 (2019); https://doi.org/10.1007/s13738-018-01577-z
N.K. Chaudhary and P. Mishra, Bioinorg. Chem. Appl., 2017, 1 (2017); https://doi.org/10.1155/2017/6927675
A.M. Khedr and H.M. Marwani, Int. J. Electrochem., 7, 10074 (2012).
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A.P. Lever, Inorganic Electronic Spectroscopy: Studies in Physical Theoretical Chemistry, Elsevier Sci., Amsterdam, edn 2, p. 33 (1984).
G.S. Kurdekar, S. Mudigoudar Puttanagouda, N.V. Kulkarni, S. Budagumpi and V.K. Revankar, Med. Chem. Res., 20, 421 (2011); https://doi.org/10.1007/s00044-010-9330-5
K.A. Melha, J. Enzyme Inhib. Med. Chem., 23, 285 (2008); https://doi.org/10.1080/14756360701448073
V.P. Singh and P. Gupta, Pharm. Chem. J., 42, 196 (2008); https://doi.org/10.1007/s11094-008-0095-9
M.M. Hamada, A.H.M. Shallaby, O. El-Shafai and A.A. El-Asmy, Transition Met. Chem., 31, 522 (2006); https://doi.org/10.1007/s11243-006-0021-5
M.K. Biyala, K. Sharma, M. Swami, N. Fahmi and R.V. Singh, Transit. Met. Chem., 33, 377 (2008); https://doi.org/10.1007/s11243-008-9053-3
R. Singh, N. Fahmi and M. Biyala, J. Iran. Chem. Soc., 2, 40 (2005); https://doi.org/10.1007/BF03245778
M.Y. Nassar, H.M. Aly, E.A. Abdelrahman and M.E. Moustafa, J. Mol. Struct., 1143, 462 (2017); https://doi.org/10.1016/j.molstruc.2017.04.118
M. Chaurasia, D. Tomar and S. Chandra, J. Mol. Struct., 1179, 431 (2019); https://doi.org/10.1016/j.molstruc.2018.11.027
M. Shabbir, Z. Akhter, I. Ahmad, S. Ahmed, V. McKee, H. Ismail and B. Mirza, Polyhedron, 124, 117 (2017); https://doi.org/10.1016/j.poly.2016.12.039