TY - JOUR
T1 - Quinolinyl Triazole Derivatives-Dominant Inhibitors for Mild Steel in Hydrochloric Acid
AU - Shetty, Nitin Kumar
AU - Tasvi Shetty, Pushpanjali
N1 - Publisher Copyright:
© 2022, Iranian Institute of Research and Development in Chemical Industries. All rights reserved.
PY - 2022/8
Y1 - 2022/8
N2 - Quinolinyl triazole derivatives 4-(4-chlorophenyl)-5-{[(5-chloroquinolin-8-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (4-4CPCQMT), 4-(3-chlorophenyl)-5-{[(5-chloroquinolin-8-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (4-3CPCQMT) and 4-(4-fluorophenyl)-5-{[(5-chloroquinolin-8-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (4-4FPCQMT) are of great importance in pharmaceutical chemistry such as antifungal, antituberculosis, anticonvulsant, anticancer activities, etc. The present work highlights the synthesis of the quinolinyl triazole derivatives ((4-4CPCQMT, 4-3CPCQMTand 4-4FPCQMT). The substituents present and the compounds 4-4CPCQMT, 4-3CPCQMTand 4-4FPCQMT were confirmed by FT-IR and NMR spectroscopy. These compounds having many reactive sites were used as inhibitors for mild steel in 1.0 M hydrochloric acid medium at 303 to 323K. An inhibition study was done by electrochemical measurement. The prevention efficiency is in the order 4-4FPCQMT>4-4CPCQMT>4-3CPCQMT. The surface morphology of the mild steel surface was done using SEM, AFM, and, EDX.
AB - Quinolinyl triazole derivatives 4-(4-chlorophenyl)-5-{[(5-chloroquinolin-8-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (4-4CPCQMT), 4-(3-chlorophenyl)-5-{[(5-chloroquinolin-8-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (4-3CPCQMT) and 4-(4-fluorophenyl)-5-{[(5-chloroquinolin-8-yl)oxy]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (4-4FPCQMT) are of great importance in pharmaceutical chemistry such as antifungal, antituberculosis, anticonvulsant, anticancer activities, etc. The present work highlights the synthesis of the quinolinyl triazole derivatives ((4-4CPCQMT, 4-3CPCQMTand 4-4FPCQMT). The substituents present and the compounds 4-4CPCQMT, 4-3CPCQMTand 4-4FPCQMT were confirmed by FT-IR and NMR spectroscopy. These compounds having many reactive sites were used as inhibitors for mild steel in 1.0 M hydrochloric acid medium at 303 to 323K. An inhibition study was done by electrochemical measurement. The prevention efficiency is in the order 4-4FPCQMT>4-4CPCQMT>4-3CPCQMT. The surface morphology of the mild steel surface was done using SEM, AFM, and, EDX.
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U2 - 10.30492/IJCCE.2021.531825.4785
DO - 10.30492/IJCCE.2021.531825.4785
M3 - Article
AN - SCOPUS:85152275904
SN - 1021-9986
VL - 41
SP - 2650
EP - 2667
JO - Iranian Journal of Chemistry and Chemical Engineering
JF - Iranian Journal of Chemistry and Chemical Engineering
IS - 8
ER -