Copyright (c) 2023 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis, Antimicrobial and Corrosion Inhibition Studies of 1,3-Benzothiazole Derivatives
Corresponding Author(s) : Ramesh S. Bhat
Asian Journal of Chemistry,
Vol. 35 No. 2 (2023): Vol 35 Issue 2, 2023
Abstract
With an emphasis on potential medicinal and corrosion inhibition applications, four N-(4-(substituted benzylidene)benzo[d]thiazol-2-amine were synthesized by the condensation of 2,3-dihydro-1,3-benzothiazol-2-amine with 4-substituted benzaldehydes. Nuclear magnetic resonance (NMR), infrared (IR) and mass spectroscopy were used to characterize the synthesized compounds. To assess the antibacterial activity of synthetic drugs, the conventional serial dilution approach has been used. The synthesized compounds showed excellent bioactivities comparable to those of a typical medication. The corrosion inhibition effect of benzothiazole derivatives has been investigated against mild steel in 0.1 N HCl solution using potentiodynamic polarization and electrochemical impedance spectroscopy methods at room temperature. The results revealed that 4-{[(1,3-benzothiazol-2-yl)imino]methyl}-N,N-dimethylaniline inhibitor has high inhibition efficiency (56.39%) at room temperature for a 50 mg/L concentration when compared to other compounds.
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- E.E.A. El Aal, S.A. El Wanees, A. Farouk and S.M.A. El Haleem, Corros. Sci., 68, 14 (2013); https://doi.org/10.1016/j.corsci.2012.09.038
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- R. Rosliza, H.B. Senin and W.B.W. Nik, Colloids Surf., 312, 185 (2008); https://doi.org/10.1016/j.colsurfa.2007.06.061
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R.J. Alaimo, S.S. Pelosi and R. Freedman, J. Pharm. Sci., 67, 281 (1978); https://doi.org/10.1002/jps.2600670247
M. Singh, S.K. Singh, M. Gangwar, G. Nath and S.K. Singh, RSC Adv., 4, 19013 (2014); https://doi.org/10.1039/C4RA02649G
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D.S. Dogruer, S. Unlu, M.F. Sahin and E. Yqilada, Il Farmaco, 53, 80 (1998); https://doi.org/10.1016/S0014-827X(97)00017-7
M.A. El-Sherbeny, Arzneimittelforschung, 50, 848 (2000); https://doi.org/10.1055/s-0031-1300300
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B. Rajeeva, N. Srinivasulu and S.M. Shantakumar, E-J. Chem., 6, 775 (2009); https://doi.org/10.1155/2009/404596
R. Danzeisen, B. Schwalenstoecker, F. Gillardon, E. Buerger, V. Krzykalla, K. Klinder, L. Schild, B. Hengerer, A.C. Ludolph, C. Dorner- Ciossek and L. Kussmaul, J. Pharmacol. Exp. Ther., 316, 189 (2006); https://doi.org/10.1124/jpet.105.092312
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M.A. Quraishi and R. Sardar, Corrosion, 58, 748 (2002); https://doi.org/10.5006/1.3277657
D.S. Zinad, M. Hanoon, R.D. Salim, S.I. Ibrahim, A.A. Al-Amiery, M.S. Takriff and A.A.H. Kadhum, J. Corros. Scale Inhib., 9, 228 (2020); https://doi.org/10.17675/2305-6894-2020-9-1-14
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K. Raviprabha and R.S. Bhat, J. Fail. Anal. Prev., 19, 1464 (2019); https://doi.org/10.1007/s11668-019-00744-5
D.D.N. Singh, T.B. Singh and B. Gaur, Corros. Sci., 37, 1005 (1995); https://doi.org/10.1016/0010-938X(95)00010-H
E.E.A. El Aal, S.A. El Wanees, A. Farouk and S.M.A. El Haleem, Corros. Sci., 68, 14 (2013); https://doi.org/10.1016/j.corsci.2012.09.038
S. Safak, B. Duran, A. Yurt and G. Turkoglu, Corros. Sci., 54, 251 (2012); https://doi.org/10.1016/j.corsci.2011.09.026
H. Farooqi, M.A. Quraishi and P.A. Saini, Natural Compounds as Cooling Water Inhibitors for Cooling Systems, In Proceedings of the EUROCORR’97, vol. 2, p. 347 (1997).
V.O. Njoku, E.E. Oguzie, C. Obi and A.A. Ayuk, Adv. Chem., 10, 1125 (2014).
R. Rosliza, H.B. Senin and W.B.W. Nik, Colloids Surf., 312, 185 (2008); https://doi.org/10.1016/j.colsurfa.2007.06.061
G.M. Pinto, J. Nayak and A.N. Shetty, Mater. Chem. Phys., 125, 628 (2011); https://doi.org/10.1016/j.matchemphys.2010.10.006
M.A. Migahed, Mater. Chem. Phys., 93, 48 (2005); https://doi.org/10.1016/j.matchemphys.2005.02.003