Abstract
In this research, the focus was on preparing a number of chalcone derivatives using the Claisen-Schmidt reaction method through the reaction of some benzaldehyde derivatives with acetophenone substitutes in the presence of a basic medium represented by (NaOH) at a concentration of 10%. The benzaldehyde derivatives and acetophenone derivatives were also dissolved in ethanol at a concentration of 98%. Before starting the preparation, a number of chalcone derivatives were banned, which were prepared and referred to as [Ch1, Ch2,Ch3, Ch4, Ch5]. The substitutes that were used in the preparation were 4-chlorobenzaldehyde, 4-aminoacetophenone, benzaldehyde, 3-Nitroacetophenone, 4-Nitrobenzaldehyde. Acetophenone ,2-4-dichlorobenzaldehyde, and 4-(dimethylamino)benzaldehyde. The compounds were spectroscopically studied using FT-IR , 1H-NMR ,13C NMR, and UV-Vis spectroscopy After that, the theoretical studies of the prepared compounds as corrosion inhibitors were conducted. They were studied theoretically using the Gaussian is a general purpose computational chemistry software package. Chalconate derivatives have the capacity to serve as electron donors as anti-corrosion agents. and it was found that derivative Ch5 is more effective theoretically as a corrosion inhibitor
Keywords
Chalcones derivatives, Characterization, Corrosion inhibition, Synthesis, Theoretical studies
Subject Area
Chemistry
Article Type
Article
First Page
2933
Last Page
2945
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
How to Cite this Article
Hamad, Acer Juma; Jawad, Hamdia Hateem; and Adem, Kadhim A.
(2025)
"Synthesis, Characterization, and Theoretical Investigation of the Effectiveness as Anti-corrosion for Chalcone Derivatives,"
Baghdad Science Journal: Vol. 22:
Iss.
9, Article 10.
DOI: https://doi.org/10.21123/2411-7986.5051