Indolin-2-one derivatives as corrosion inhibitors: Structural insights and evaluation through experimental and computational techniques

被引:11
|
作者
Mansour, Abdelkarim Ait [1 ]
Lgaz, Hassane [2 ]
Allah, Abderrazzak Elmoutaouakil Ala [3 ]
Jang, JongMin [4 ]
Messali, Mouslim [5 ]
Bazzi, Lahcen [6 ]
Lee, Han-seung [4 ]
Ramli, Youssef [3 ,7 ]
Salghi, Rachid [1 ,6 ,8 ]
机构
[1] Univ Ibn Zohr, Lab Appl Chem & Environm, ENSA, POB 1136, Agadir 80000, Morocco
[2] Hanyang Univ ERICA, Innovat Durable Bldg & Infrastructure Res Ctr, Ctr Creat Convergence Educ, 55 Hanyangdaehak Ro, Ansan 15588, Gyeonggi Do, South Korea
[3] Mohammed V Univ Rabat, Fac Med & Pharm, Drug Sci Res Ctr, Lab Med Chem, Rabat, Morocco
[4] Hanyang Univ ERICA, Dept Architectural Engn, 55 Hanyangdaehak Ro, Ansan 15588, Gyeonggi Do, South Korea
[5] Imam Mohammad Ibn Saud Islamic Univ, Coll Sci, Dept Chem, POB 90950, Riyadh 11623, Saudi Arabia
[6] SupMTI, Lab Genie Ind Energet & Environm LGI2E, Rabat 10000, Morocco
[7] Mohammed VI Ctr Res & Innovat CM6, Rabat 10000, Morocco
[8] Euromed Univ Fes, Euromed Res Ctr, Euromed Polytech Sch, Ecocampus,Meknes Rd, Fes 30030, Morocco
基金
新加坡国家研究基金会;
关键词
Indolin-2-one derivatives; Corrosion inhibitors; Sustainable industrial processes; Atomistic simulations; MILD-STEEL; ACIDIC MEDIUM; CARBON-STEEL; ADSORPTION; SURFACE; HCL; MOLECULES; MECHANISM; SCAFFOLD; INDOLE;
D O I
10.1016/j.molstruc.2024.137592
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Effective corrosion management is a pivotal challenge facing various industries and holds crucial importance in aligning industrial processes with sustainability goals. This study focused on the synthesis and evaluation of two indolin-2-one derivatives: (E)-1-allyl-3-(2-(5-oxo-4,4-diphenyl-4,5-dihydro-1H-imidazol-2-yl)hydrazono)indolin2-one (AIHI) and (E)-3-(2-(5-oxo-4,4-diphenyl-4,5-dihydro-1H-imidazol-2-yl)hydrazono)-1-(prop-2-yn-1-yl) indolin-2-one (PIHI), as sustainable corrosion inhibitors for N80 carbon steel (N80CS) in a 15 wt. % HCl medium. Chemical, electrochemical, and surface characterization techniques were utilized to evaluate the corrosion inhibition mechanism and the performance of the compounds under investigation. The weight loss method highlighted that tested compounds exhibited promising inhibition efficiencies: 91.54 % for AIHI and 81.97 % for PIHI, respectively, at 303 K, with an outstanding performance of 87.17 % at 363 K for AIHI. The simultaneous addition of AIHI and PIHI in HCl led to a substantial increase in the polarization resistance (RP) and a remarkable decrease in the corrosion current density (icorr). The potentiodynamic polarization (PDP) technique validated that both indolin-2-one compounds function as anodic/cathodic corrosion inhibitors with remarkable anodic effect. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) showed that inhibitors altered steel surface morphology, forming a protective layer, and significantly reduced surface roughness. Atomistic simulations (DFT and SCC-DFTB methods) pointed out that the inhibitors AIHI and PIHI acted by physicochemical adsorption through donor-acceptor interactions between AIHI or PIHI molecules (s and p orbitals) and the 3d orbitals of Fe(110). The insights obtained serve as a foundation for future advancements in greener corrosion management strategies for sustainable industrial applications, thus reinforcing our commitment to biocircular economies and sustainable chemistry.
引用
收藏
页数:17
相关论文
共 50 条
  • [1] SYNTHESIS OF SPIRO INDOLIN-2-ONE DERIVATIVES
    ELAHL, AAS
    AFEEFY, H
    METWALLY, MA
    JOURNAL OF CHEMICAL RESEARCH-S, 1994, (01): : 14 - 15
  • [2] Preliminary evaluation of antiproliferative and apoptotic activities of novel indolin-2-one derivatives
    Turhal, Gulseren
    Demirkan, Busra
    Baslilar, Izel Nermin
    Yuncu, Nimet Sule
    Baytas, Sultan Nacak
    Demiroglu-Zergeroglu, Asuman
    DRUG DEVELOPMENT RESEARCH, 2024, 85 (05)
  • [3] Synthesis, Biological, and Computational Evaluation of Novel 1,3,5-Substituted Indolin-2-one Derivatives as Inhibitors of Src Tyrosine Kinase
    Kilic-Kurt, Zuhal
    Bakar, Filiz
    Olgen, Sureyya
    ARCHIV DER PHARMAZIE, 2015, 348 (10) : 715 - 729
  • [4] Design, synthesis and biological evaluation of novel indolin-2-one derivatives as potent second-generation TRKs inhibitors
    Qin, Qiaohua
    Fu, Qinglin
    Wang, Xin
    Lv, Ruicheng
    Lu, Shuyu
    Guo, Zhiqiang
    Wu, Tianxiao
    Sun, Yin
    Sun, Yixiang
    Liu, Nian
    Zhao, Dongmei
    Cheng, Maosheng
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 253
  • [5] Indolin-2-one derivatives as selective Aurora B kinase inhibitors targeting breast cancer
    Dokla, Eman M. E.
    Abdel-Aziz, Amal Kamal
    Milik, Sandra N.
    Mahmoud, Amr H.
    Saadeldin, Mona Kamal
    McPhillie, Martin J.
    Minucci, Saverio
    Abouzid, Khaled A. M.
    BIOORGANIC CHEMISTRY, 2021, 117
  • [6] The Development of 3-substituted Indolin-2-one Derivatives as Kinase Inhibitors for Cancer Therapy
    Xu, Changqing
    Liu, Yang
    Zhao, Guisen
    CURRENT MEDICINAL CHEMISTRY, 2022, 29 (11) : 1891 - 1919
  • [7] Synthesis and Biological Evaluation of Novel Indolin-2-One Derivatives as Protein Tyrosine Phosphatase 1B Inhibitors
    Dai, Hou-Ling
    Shen, Qiang
    Zheng, Jian-Bin
    Li, Jing-Ya
    Wen, Ren
    Li, Jia
    LETTERS IN ORGANIC CHEMISTRY, 2011, 8 (07) : 526 - 530
  • [8] Synthesis and antiproliferative evaluation of piperazine-1-carbothiohydrazide derivatives of indolin-2-one
    Lin, Hui-Hui
    Wu, Wei-Yao
    Cao, Sheng-Li
    Liao, Ji
    Ma, Li
    Gao, Man
    Li, Zhong-Feng
    Xu, Xingzhi
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (11) : 3304 - 3307
  • [9] THE INVESTIGATION OF BENZ[C,D]INDOLIN-2-ONE DERIVATIVES - THE BROMINATION OF BENZ[C,D]INDOLIN-2-ONE CARBOXYLIC-ACIDS
    BYSTRITSKII, GI
    RODIONOVA, GN
    YELETSKAYA, SV
    SHEBAN, GV
    VOROZHTSOV, GN
    ZAITSEV, BY
    PARTALLA, NA
    KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII, 1985, (10): : 1363 - 1367
  • [10] Crystal and Molecular Structural Features of Indolin-2-One Derivatives with Sterically Hindered Phenol Moieties
    E. V. Mironova
    A. V. Bogdanov
    G. N. Nugumanova
    S. V. Bukharov
    V. F. Mironov
    I. A. Litvinov
    Journal of Structural Chemistry, 2018, 59 : 439 - 448