Abstract
Herein, novel 5-arylazosalicylaldehyde thiosemicarbazone derivatives (H2L1–12) and their copper(II) complexes have been synthesized and characterized by NMR, IR and UV-Vis spectra and TGA/DTA. The accumulated data exhibit that thiosemicarbazone derivatives bind with copper ion via the deprotonated phenolic-OH, azomethine-N and deprotonated thiol-SH groups. Accordingly, composition of the complexes can be presented as CuL·H2O. The TGA analysis of Cu(II) complexes have revealed their thermal stability up to ca. 170°C.
Similar content being viewed by others
REFERENCES
El-Sharief, M.A.M.S., Abbas, S.Y., El-Bayouki, K.A.M., and El-Gammal, E.W., Eur. J. Med. Chem., 2013, vol. 67, p. 263. https://doi.org/10.1016/j.ejmech.2013.06.031
Khalilian, M.H., Mirzaeia, S., and Taherpour, A., New J. Chem., 2015, vol. 39, p. 9313. https://doi.org/10.1039/C5NJ02041G
Abbas, S.Y., Farag, A.A., Ammar, Y.A., Atrees, A.A., Mohamed, A.F., and El-Henawy, A.A., Monatsh Chem., 2013, vol. 144, p. 1725. https://doi.org/10.1007/s00706-013-1034-3
Abbas, S.Y., Basyouni, W.M., El-Bayouki, K.A.M., Dawood, R.M., Abdelhafez, T.H., and Elawady, M.K., Synthetic Commun., 2019, vol. 49, p. 2411. https://doi.org/10.1080/00397911.2019.1626893
Basyouni, W.M., Abbas, S.Y., El-Bayouki, K.A.M., Dawood, R.M., and Elawady, M.K., Synthetic Commun., 2021, in press. https://doi.org/10.1080/00397911.2021.1925298
Eissa, S.I., Farrag, A.M., Abbas, S.Y., El Shehry, M.F., Ragab, A., Fayed, E.A., and Ammar, Y.A., Bioorg. Chem., 2021, vol. 110, p. 104803. https://doi.org/10.1016/j.bioorg.2021.104803
Bauer, D.J. and Sheffield, F.W., Nature, 1959, vol. 184, p. 1496.
Trondl, R., Flocke, L.S., Kowol, C.R., Heffeter, P., Jungwirth, U., Mair, G.E., Steinborn, R., Enyedy, E.A., Jakupec, M.A., Berger, W., and Keppler, B.K., Mol. Pharmacol., 2014, vol. 85, p. 451. https://doi.org/10.1124/mol.113.090605
Petrasheuskaya, T.V., Kiss, M.A., Domotor, O., Holczbauer, T., May, N.V., Spengler, G., Kincses, A., Gasparovic, A.C., Frank, E., and Enyedy, E.A., New J. Chem., 2020, vol. 44, p. 12154. https://doi.org/10.1039/D0NJ01070G
Dkhar, L., Banothu, V., Poluri, K.M., Kaminsky, W., and Kollipara, M.R., J. Organomet. Chem., 2020, vol. 918, p. 121298. https://doi.org/10.1016/j.jorganchem.2020.121298
Abbas, S.Y., Basyouni, W.M., and El-Bayouki, K.A.M., J. Mol. Struct., 2013, vol. 1050, p. 192. https://doi.org/10.1016/j.molstruc.2013.07.033
Abbas, S.Y., Basyouni, W.M., and El-Bayouki, K.A.M., Appl. Organomet. Chem., 2018. vol. 32 (2), p. e4032. https://doi.org/10.1002/aoc.4032
Singh, B., and Srivastava, U., Synth. React. Inorg. Met.-Org. Chem., 1989, vol. 19, p. 279. https://doi.org/10.1080/00945718908048069
Lu, Z., Whyte, A.C., Rheingold, A.L., and Crabtree, R.H., Inorg. Chem., 1993, vol. 32, p. 3991. https://doi.org/10.1021/ic00071a006
West, D.X., Salberg, M.M., Bain, G.A., Liberta, A.E., Martinez, J.V., and Ortega, S.H., Transition Met. Chem., 1996, vol. 21, p. 206. https://doi.org/10.1007/BF00165968
Chatterjee, M. and Ghosh, S., Transition Met. Chem., 1998, vol. 23, p. 355. https://doi.org/10.1023/A:1006930013688
Funding
The authors extend their appreciation to the Deanship of Scientific Research at King Khalid University for funding this work under grant number: R.G.P.1/231/41.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
No conflict of interest was declared by the authors.
Rights and permissions
About this article
Cite this article
Salem, M.A., Abbas, S.Y., Darwish, S.A. et al. Synthesis of Novel Tridentate 5-Arylazosalicylaldehyde Thiosemicarbazone Derivatives and Their Complexes with Copper(II). Russ J Gen Chem 91, 1578–1583 (2021). https://doi.org/10.1134/S1070363221080211
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070363221080211