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Retraction: Design of 1-methylimidazolium tricyanomethanide as the first nanostructured molten salt and its catalytic application in the condensation reaction of various aromatic aldehydes, amides and β-naphthol compared with tin dioxide nanoparticles

Mohammad Ali Zolfigol*a, Saeed Bagherya, Ahmad Reza Moosavi-Zare*b, Seyed Mohammad Vahdatc, Heshmatollah Alinezhadd and Mohammad Norouzide
aFaculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, Iran. E-mail: zolfi@basu.ac.ir; mzolfigol@yahoo.com; Fax: +98 8138257407
bDepartment of Chemistry, University of Sayyed Jamaleddin Asadabadi, Asadabad 6541835583, Iran. E-mail: moosavizare@yahoo.com
cDepartment of Chemistry, Ayatollah Amoli Branch, Islamic Azad University, P.O. Box 678, Amol, Iran
dFaculty of Chemistry, University of Mazandaran, Babolsar 47415, Iran
eDepartment of Chemistry, Payame Noor University, P.O. Box 19395-3697, Tehran, Iran

Received 6th September 2022 , Accepted 6th September 2022

First published on 26th September 2022


Abstract

Retraction of ‘Design of 1-methylimidazolium tricyanomethanide as the first nanostructured molten salt and its catalytic application in the condensation reaction of various aromatic aldehydes, amides and β-naphthol compared with tin dioxide nanoparticles’ by Mohammad Ali Zolfigol et al., RSC Adv., 2015, 5, 45027–45037, https://doi.org/10.1039/C5RA02718G.


The Royal Society of Chemistry hereby wholly retracts this RSC Advances article as the synthesis of 1-methylimidazolium tricyanomethanide reported in the article, whereby tricyanomethane is used as a starting material, is not reproducible. The authors stated that they did not report the synthesis of tricyanomethane in the published paper as they purchased this compound from a commercial center and used it in the synthesis of ionic liquids, molten salts and various kinds of catalysts. The authors thought the reaction between tricyanomethane and organic bases is a simple acid–base reaction, therefore they did not cite the previously reported literature and its related history for the preparation of tricyanomethane. However, according to papers by Banert et al.,1,2 and based on their obtained analysis of the chemical sold to them as tricyanomethane, it became clear to the authors that this purchased compound was not tricyanomethane as there were differences in the 1H NMR and 13C NMR chemical shift between the purchased compound and the reports of Banert et al.1 According to these documents, the authors believe that the compound sold to them as tricyanomethane was fake. While the authors have now re-prepared 1-methylimadazolium tricyanomethanide, by synthesising potassium tricyanomethanide as a starting material for the synthesis,3–5 the synthesis reported in this article is not accurate. Therefore, this article is being retracted to avoid misleading readers and to protect the accuracy and integrity of the scientific record.

Mohammad Ali Zolfigol, Saeed Baghery and Ahmad Reza Moosavi-Zare oppose the retraction. Seyed Mohammad Vahdat, Heshmatollah Alinezhad and Mohammad Norouzi were contacted but did not respond.

Signed: Laura Fisher, Executive Editor, RSC Advances

Date: 17th August 2022

References

  1. K. Banert and M. Hagedorn, Synlett, 2019, 30, 1427 CrossRef CAS.
  2. K. Banert, M. Chityala, M. Hagedorn, H. Beckers, T. Stueker, S. Riedel, T. Rueffer and H. Lang, Angew. Chem., Int. Ed., 2017, 56, 9582 CrossRef CAS PubMed.
  3. S. Trofimenko, E. L. Little and H. F. Mower, J. Org. Chem., 1962, 27, 433 CrossRef CAS.
  4. R. A. Carboni, Org. Synth., 1959, 39, 64 CrossRef CAS.
  5. R. C. Beaumont, K. B. Aspin, T. J. Demas, J. H. Hoggatt and G. E. Potter, Inorg. Chim. Acta, 1984, 84, 141 CrossRef CAS.

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