Copyright (c) 2018 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Characterization of Palladium(II) Complexes with Thiosemicarbazones
Corresponding Author(s) : Geetika Borah
Asian Journal of Chemistry,
Vol. 30 No. 6 (2018): Vol 30 Issue 6
Abstract
Three new complexes viz., [PdCl2(H-aatp)2] (1), [Pd(dmbptz)2] (2) and [Pd(btz)] (3) have been synthesized by reacting [PdCl2(cod)] with the ligands H-aatp, H-dmbptz and H2-btz, respectively (where H-aatp = anisaldene-4-aminothiophenol; H-dmbptz = 2,5-dimethoxybenzyl-4-phenylthiosemicarbazone and H2-btz = benzil-bisthiosemicarbazone). These have been characterized by various physico-chemical techniques such as FTIR, UV-visible, 1H and 13C NMR, ESI(+)-mass spectroscopy, etc. The complexes were found to be diamagnetic, four coordinated mononuclear neutral molecules with square planar or distorted square planar geometry.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- R.N. Prabhu and R. Ramesh, Tetrahedron Lett., 57, 4893 (2016); https://doi.org/10.1016/j.tetlet.2016.09.049.
- T.S. Lobana, P. Kumari, G. Hundal, R.J. Butcher, A. Castineiras and T. Akitsu, Inorg. Chim. Acta, 394, 605 (2013); https://doi.org/10.1016/j.ica.2012.09.021.
- D. Kumar and V.K. Singh, J. Drug Disc. Therap., 2, 24 (2014).
- P. Chellan, T. Stringer, A. Shokar, P.J. Dornbush, G. Vazquez-Anaya, K.M. Land, K. Chibale and G.S. Smith, J. Inorg. Biochem., 105, 1562 (2011); https://doi.org/10.1016/j.jinorgbio.2011.07.023.
- M.X. Li, C.L. Chen, D. Zhang, J.Y. Niu and B.S. Ji, Eur. J. Med. Chem., 45, 3169 (2010); https://doi.org/10.1016/j.ejmech.2010.04.009.
- S. Datta, M.G.B. Drew and S. Bhattacharya, Indian J. Chem., 50A, 1403 (2011)
- J. Martínez, E.M. Cabaleiro-Lago, J.M. Ortigueira, M.T. Pereira, P. Frieiro, F. Lucio and J.M. Vila, Inorg. Chim. Acta, 449, 20 (2016); https://doi.org/10.1016/j.ica.2016.03.044.
- A.D. Khalaji, E. Shahsavani, N. Feizi, M. Kuceraková, M. Dusek, R. Mazandarani and A. Amiri, C.R. Chim., 20, 125 (2017); https://doi.org/10.1016/j.crci.2016.05.009.
- J.G. Da Silva, C.C.H. Perdigao, N.L. Speziali and H. Beraldo, J. Coord. Chem., 66, 385 (2013); https://doi.org/10.1080/00958972.2012.757762.
- G. Borah, J. Baruah and D. Kardong, Indian J. Chem., 53A, 1520 (2014).
- M.A. Salam, M.A. Hussein, I. Ramli and M.S. Islam, J. Organomet. Chem., 813, 71 (2016); https://doi.org/10.1016/j.jorganchem.2016.04.007.
- A. Dobrova, S. Platzer, F. Bacher, M.N.M. Milunovic, A. Dobrov, G. Spengler, É.A. Enyedy, G. Novitchi and V.B. Arion, Dalton Trans., 45, 13427 (2016); https://doi.org/10.1039/C6DT02784A.
- N. Nanjundan, R. Narayanasamy, R.J. Butcher, J.P. Jasinski, K. Velmurugan, R. Nandhakumar, M.D. Balakumaran, P.T. Kalaichelvan and V.G. Gnanasoundari, Inorg. Chim. Acta, 455, 283 (2017); https://doi.org/10.1016/j.ica.2016.10.035.
- A. Molter and F. Mohr, Polyhedron, 120, 118 (2016); https://doi.org/10.1016/j.poly.2016.07.016.
- R. Deb, P. Paul and S. Bhattacharya, Proc. Natl. Acad. Sci. India Sect. A Phys. Sci., 86, 551 (2016); https://doi.org/10.1007/s40010-016-0303-z.
- E.Z. Jahromi, A. Divsalar, A.A. Saboury, S. Khaleghizadeh, H. MansouriTorshizi and I. Kostova, J. Iran. Chem. Soc., 13, 967 (2016); https://doi.org/10.1007/s13738-015-0804-8.
- R. Manikandan, P. Anitha, P. Viswanathamurthi and J.G. Malecki, Polyhedron, 119, 300 (2016); https://doi.org/10.1016/j.poly.2016.09.005.
- D. Drew and J.R. Doyle, Inorg. Synth., 13, 47 (1972).
- S. Chandra, S. Raizada, M. Tyagi and A. Gautam, Bioinorg. Chem. Appl., Article ID 51483 (2007); https://doi.org/10.1155/2007/51483.
- D. Sutton, Electronic Spectra of Transition Metal Complexes: An Introductory Text, McGraw-Hill Publishing Company Limited, p. 192 (1968).
References
R.N. Prabhu and R. Ramesh, Tetrahedron Lett., 57, 4893 (2016); https://doi.org/10.1016/j.tetlet.2016.09.049.
T.S. Lobana, P. Kumari, G. Hundal, R.J. Butcher, A. Castineiras and T. Akitsu, Inorg. Chim. Acta, 394, 605 (2013); https://doi.org/10.1016/j.ica.2012.09.021.
D. Kumar and V.K. Singh, J. Drug Disc. Therap., 2, 24 (2014).
P. Chellan, T. Stringer, A. Shokar, P.J. Dornbush, G. Vazquez-Anaya, K.M. Land, K. Chibale and G.S. Smith, J. Inorg. Biochem., 105, 1562 (2011); https://doi.org/10.1016/j.jinorgbio.2011.07.023.
M.X. Li, C.L. Chen, D. Zhang, J.Y. Niu and B.S. Ji, Eur. J. Med. Chem., 45, 3169 (2010); https://doi.org/10.1016/j.ejmech.2010.04.009.
S. Datta, M.G.B. Drew and S. Bhattacharya, Indian J. Chem., 50A, 1403 (2011)
J. Martínez, E.M. Cabaleiro-Lago, J.M. Ortigueira, M.T. Pereira, P. Frieiro, F. Lucio and J.M. Vila, Inorg. Chim. Acta, 449, 20 (2016); https://doi.org/10.1016/j.ica.2016.03.044.
A.D. Khalaji, E. Shahsavani, N. Feizi, M. Kuceraková, M. Dusek, R. Mazandarani and A. Amiri, C.R. Chim., 20, 125 (2017); https://doi.org/10.1016/j.crci.2016.05.009.
J.G. Da Silva, C.C.H. Perdigao, N.L. Speziali and H. Beraldo, J. Coord. Chem., 66, 385 (2013); https://doi.org/10.1080/00958972.2012.757762.
G. Borah, J. Baruah and D. Kardong, Indian J. Chem., 53A, 1520 (2014).
M.A. Salam, M.A. Hussein, I. Ramli and M.S. Islam, J. Organomet. Chem., 813, 71 (2016); https://doi.org/10.1016/j.jorganchem.2016.04.007.
A. Dobrova, S. Platzer, F. Bacher, M.N.M. Milunovic, A. Dobrov, G. Spengler, É.A. Enyedy, G. Novitchi and V.B. Arion, Dalton Trans., 45, 13427 (2016); https://doi.org/10.1039/C6DT02784A.
N. Nanjundan, R. Narayanasamy, R.J. Butcher, J.P. Jasinski, K. Velmurugan, R. Nandhakumar, M.D. Balakumaran, P.T. Kalaichelvan and V.G. Gnanasoundari, Inorg. Chim. Acta, 455, 283 (2017); https://doi.org/10.1016/j.ica.2016.10.035.
A. Molter and F. Mohr, Polyhedron, 120, 118 (2016); https://doi.org/10.1016/j.poly.2016.07.016.
R. Deb, P. Paul and S. Bhattacharya, Proc. Natl. Acad. Sci. India Sect. A Phys. Sci., 86, 551 (2016); https://doi.org/10.1007/s40010-016-0303-z.
E.Z. Jahromi, A. Divsalar, A.A. Saboury, S. Khaleghizadeh, H. MansouriTorshizi and I. Kostova, J. Iran. Chem. Soc., 13, 967 (2016); https://doi.org/10.1007/s13738-015-0804-8.
R. Manikandan, P. Anitha, P. Viswanathamurthi and J.G. Malecki, Polyhedron, 119, 300 (2016); https://doi.org/10.1016/j.poly.2016.09.005.
D. Drew and J.R. Doyle, Inorg. Synth., 13, 47 (1972).
S. Chandra, S. Raizada, M. Tyagi and A. Gautam, Bioinorg. Chem. Appl., Article ID 51483 (2007); https://doi.org/10.1155/2007/51483.
D. Sutton, Electronic Spectra of Transition Metal Complexes: An Introductory Text, McGraw-Hill Publishing Company Limited, p. 192 (1968).