TY - JOUR
T1 - Structural elucidation of a novel dual-substituted thiosemicarbazone scaffold as an efficient copper corrosion inhibitor
T2 - Insights from RSM, XPS, and DFT–Fukui analyses
AU - Alwi, Muhammad Ammar Mohamad
AU - Ahmad, Mohammad Norazmi
AU - Kayed, Safa Faris
AU - Dzulkifli, Nur Nadia
AU - Samah, Mohd Armi Abu
AU - Pauzi, Hariy
AU - Normaya, Erna
N1 - Publisher Copyright:
© 2025
PY - 2026/4/5
Y1 - 2026/4/5
N2 - Copper corrosion in acidic environments poses significant challenges in industrial systems, yet limited research has explored dual substitution within thiosemicarbazone scaffolds to enhance adsorption behavior and establish structure–reactivity correlations. This study reports the structural elucidation and inhibition performance of a newly designed dual-substituted thiosemicarbazone inhibitor, pyrazinyl–thiosemicarbazone–aminophenyl (PZTAP), developed for efficient copper protection in hydrochloric acid. The molecule integrates a pyrazinyl ring at N(1) and a 2-aminophenyl group at N(4), forming a conjugated donor–acceptor system that strengthens surface interactions. Corrosion inhibition was evaluated using gravimetric and electrochemical impedance spectroscopy (EIS), with optimization via response surface methodology (RSM). Under optimal conditions (40.95 °C, 2.65 M HCl, 0.63 mM, 12.55 h), PZTAP achieved inhibition efficiencies of 93.78 % (weight loss) and 94.32 % (EIS), with strong agreement between predicted and experimental models (R² > 0.99, CV < 2 %). Langmuir isotherm fitting revealed a spontaneous chemisorption mechanism (ΔG°ads = −40.83 kJ mol⁻¹), supported by Cu–N and Cu–S bonding identified by X-ray photoelectron spectroscopy. Scanning electron microscopy confirmed the formation of a protective surface film. Theoretical results showed a favorable HOMO–LUMO gap (4.04 eV), high HOMO energy (−6.33 eV), and notable global softness (0.4957 eV⁻¹), correlating with efficient electron donation to copper. Molecular electrostatic potential (MEP) and Fukui function analyses identified C = S and C = N groups as dominant nucleophilic adsorption centers. This integrated experimental–theoretical investigation demonstrates that dual substitution significantly enhances donor–acceptor interactions and adsorption strength, establishing PZTAP as a high-efficiency, structure-guided corrosion inhibitor for copper in acidic media.
AB - Copper corrosion in acidic environments poses significant challenges in industrial systems, yet limited research has explored dual substitution within thiosemicarbazone scaffolds to enhance adsorption behavior and establish structure–reactivity correlations. This study reports the structural elucidation and inhibition performance of a newly designed dual-substituted thiosemicarbazone inhibitor, pyrazinyl–thiosemicarbazone–aminophenyl (PZTAP), developed for efficient copper protection in hydrochloric acid. The molecule integrates a pyrazinyl ring at N(1) and a 2-aminophenyl group at N(4), forming a conjugated donor–acceptor system that strengthens surface interactions. Corrosion inhibition was evaluated using gravimetric and electrochemical impedance spectroscopy (EIS), with optimization via response surface methodology (RSM). Under optimal conditions (40.95 °C, 2.65 M HCl, 0.63 mM, 12.55 h), PZTAP achieved inhibition efficiencies of 93.78 % (weight loss) and 94.32 % (EIS), with strong agreement between predicted and experimental models (R² > 0.99, CV < 2 %). Langmuir isotherm fitting revealed a spontaneous chemisorption mechanism (ΔG°ads = −40.83 kJ mol⁻¹), supported by Cu–N and Cu–S bonding identified by X-ray photoelectron spectroscopy. Scanning electron microscopy confirmed the formation of a protective surface film. Theoretical results showed a favorable HOMO–LUMO gap (4.04 eV), high HOMO energy (−6.33 eV), and notable global softness (0.4957 eV⁻¹), correlating with efficient electron donation to copper. Molecular electrostatic potential (MEP) and Fukui function analyses identified C = S and C = N groups as dominant nucleophilic adsorption centers. This integrated experimental–theoretical investigation demonstrates that dual substitution significantly enhances donor–acceptor interactions and adsorption strength, establishing PZTAP as a high-efficiency, structure-guided corrosion inhibitor for copper in acidic media.
KW - Copper corrosion inhibition
KW - density functional theory (DFT–Fukui analysis)
KW - Dual-substituted thiosemicarbazone scaffold
KW - Response surface methodology (RSM)
KW - Structural elucidation
KW - X-ray photoelectron spectroscopy (XPS)
UR - https://www.scopus.com/pages/publications/105025032460
U2 - 10.1016/j.molstruc.2025.145021
DO - 10.1016/j.molstruc.2025.145021
M3 - Article
AN - SCOPUS:105025032460
SN - 0022-2860
VL - 1356
JO - Journal of Molecular Structure
JF - Journal of Molecular Structure
M1 - 145021
ER -