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Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative

A new 8-hydroxyquinoline derivative, namely 1,3-bis(quinoline-8-dimethylformamide) propane (BQYP), was synthesized and characterized by different spectral methods, such as (1)H NMR, (13)C NMR, and FTIR spectra. The anticorrosive properties of the BQYP molecule against the corrosion of mild steel wer...

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Autores principales: Alamshany, Zahra M., Ganash, Aisha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889052/
https://www.ncbi.nlm.nih.gov/pubmed/31844761
http://dx.doi.org/10.1016/j.heliyon.2019.e02895
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author Alamshany, Zahra M.
Ganash, Aisha A.
author_facet Alamshany, Zahra M.
Ganash, Aisha A.
author_sort Alamshany, Zahra M.
collection PubMed
description A new 8-hydroxyquinoline derivative, namely 1,3-bis(quinoline-8-dimethylformamide) propane (BQYP), was synthesized and characterized by different spectral methods, such as (1)H NMR, (13)C NMR, and FTIR spectra. The anticorrosive properties of the BQYP molecule against the corrosion of mild steel were tested in 2 M Η(2)SO(4) acid with a varied range of concentrations (0.05–1 mM) at different temperatures using the electrochemical technique. It was clear that adsorption acted according to Langmuir's relationship. The inhibition effect improved with increases in concentration of inhibitor (~91% for 1 mM at 298 °K) and was reduced with increasing temperature. Finally, the density functional theory (DFT), with bases set according to the B3LYP/6-311+G (d,p) level, was used for calculating the quantum parameter to explain the effect of the electronic structure of the BQYP molecule on providing the experimental findings.
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spelling pubmed-68890522019-12-16 Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative Alamshany, Zahra M. Ganash, Aisha A. Heliyon Article A new 8-hydroxyquinoline derivative, namely 1,3-bis(quinoline-8-dimethylformamide) propane (BQYP), was synthesized and characterized by different spectral methods, such as (1)H NMR, (13)C NMR, and FTIR spectra. The anticorrosive properties of the BQYP molecule against the corrosion of mild steel were tested in 2 M Η(2)SO(4) acid with a varied range of concentrations (0.05–1 mM) at different temperatures using the electrochemical technique. It was clear that adsorption acted according to Langmuir's relationship. The inhibition effect improved with increases in concentration of inhibitor (~91% for 1 mM at 298 °K) and was reduced with increasing temperature. Finally, the density functional theory (DFT), with bases set according to the B3LYP/6-311+G (d,p) level, was used for calculating the quantum parameter to explain the effect of the electronic structure of the BQYP molecule on providing the experimental findings. Elsevier 2019-11-26 /pmc/articles/PMC6889052/ /pubmed/31844761 http://dx.doi.org/10.1016/j.heliyon.2019.e02895 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alamshany, Zahra M.
Ganash, Aisha A.
Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
title Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
title_full Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
title_fullStr Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
title_full_unstemmed Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
title_short Synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
title_sort synthesis, characterization, and anti-corrosion properties of an 8-hydroxyquinoline derivative
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889052/
https://www.ncbi.nlm.nih.gov/pubmed/31844761
http://dx.doi.org/10.1016/j.heliyon.2019.e02895
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