Evidence map›Paper›PMID 39866633›Full record

ArticleACS omega2025

An Investigation into the Synthesis and Characterization of Novel Tetrazole Derivatives for Application as Mild Steel Corrosion Inhibitors in a Solution of Hydrochloric Acid.

Riham Sghyar, Yassine Rhazi, Mourad Aloui, Mouad Lahyaoui, Hajar Elmrayej, Hicham Elmsellem, Omar Abdellaoui, Noura Aflak, Oussama Moussaoui, Mohammed M Alanazi and 4 more

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Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Riham SghyarLaboratory of Applied Organic Chemistry, Faculty of Science and Techniques, Sidi Mohamed Ben Abdellah University, B.P. 2202, Routed Imouzzer, Fez 30050, Morocco.
Yassine RhaziLaboratory of Engineering, Organometallic, Molecular and Environment (LIMOME), Faculty of Science, Université Sidi Mohamed Ben Abdellah, Fez 30000, Morocco.
Mourad AlouiLIMAS Laboratory, Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, Fez 30000, Morocco.
Mouad LahyaouiLaboratory of Applied Organic Chemistry, Faculty of Science and Techniques, Sidi Mohamed Ben Abdellah University, B.P. 2202, Routed Imouzzer, Fez 30050, Morocco.ORCID https://orcid.org/0000-0002-8068-7177
Hajar ElmrayejLaboratory of Engineering, Electrochemistry, Modeling and Environment, Faculty of Sciences, Sidi Mohamed Ben Abdellah University, Fez 30000, Morocco.
Hicham ElmsellemLaboratory of Applied Chemistry and Environment (LCAE). Department of Chemistry, Faculty of Sciences, University Mohamed I, Oujda 60000, Morocco.
Omar AbdellaouiLaboratory of Applied Organic Chemistry, Faculty of Science and Techniques, Sidi Mohamed Ben Abdellah University, B.P. 2202, Routed Imouzzer, Fez 30050, Morocco.
Noura AflakTeam of Organic Chemistry and Valorization of Natural Substances (OCVNS), FSA, Ibn Zohr University, Agadir 80000, Morocco.ORCID https://orcid.org/0000-0002-6396-2114
Oussama MoussaouiLaboratory of Applied Organic Chemistry, Faculty of Science and Techniques, Sidi Mohamed Ben Abdellah University, B.P. 2202, Routed Imouzzer, Fez 30050, Morocco.
Mohammed M AlanaziDepartment of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Atul KabraUniversity Institute of Pharma Sciences, Chandigarh University, Mohali, Punjab 140301, India.
El Mestafa El HadramiLaboratory of Applied Organic Chemistry, Faculty of Science and Techniques, Sidi Mohamed Ben Abdellah University, B.P. 2202, Routed Imouzzer, Fez 30050, Morocco.
El Houssine MabroukLIMAS Laboratory, Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, Fez 30000, Morocco.
Nada Kheira SebbarDepartment of Applied Chemistry, Faculty of Applied Sciences Ait Melloul, Ibn Zohr University, Agadir 60000, Morocco.ORCID https://orcid.org/0000-0003-4944-1010

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of the study was to synthesize tetrazole molecules featuring nitro groups positioned at the para and meta locations. We aimed to assess their effectiveness in inhibiting corrosion of mild steel in a 1 M HCl solution at 298 K. Tetrazoles with 2,5-disubstitution were created using [3 + 2] cycloaddition and N-alkylation techniques, with a particular emphasis on synthesizing molecules that contain nitro groups. Tafel polarization experiments, which employ the polarization curve approach, were used to assess the effectiveness of corrosion inhibition. Furthermore, quantum chemical calculations using density functional theory and Monte Carlo simulations were used to investigate the connection between the molecular structure of the produced tetrazoles and their efficacy as corrosion inhibitors. The results showed that the 2,5-disubstituted tetrazoles exhibited high corrosion inhibition efficiencies, with compounds

Identifiers

PMID39866633
PMCPMC11755168

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