Eka Helena Sinaga , Yoga Romdoni , Bayu Ardiansah , Rika Tri Yunarti , Budi Riza Putra , Wulan Tri Wahyuni , Munawar Khalil
{"title":"Activity of two-dimensional Cr2CTx MXene for the synthesis of Eugenol-1,2,3-Triazole via click chemistry","authors":"Eka Helena Sinaga , Yoga Romdoni , Bayu Ardiansah , Rika Tri Yunarti , Budi Riza Putra , Wulan Tri Wahyuni , Munawar Khalil","doi":"10.1016/j.inoche.2025.115537","DOIUrl":null,"url":null,"abstract":"<div><div>The development of efficient heterogeneous catalysts for the synthesis of heterocyclic compounds is crucial for various applications. In this work, two-dimensional Cr<sub>2</sub>CT<sub>x</sub> MXene was successfully synthesized via a selective etching method using HF and HCl. Its formation and structural properties were comprehensively verified using various characterization techniques, including XRD, FTIR, Raman spectroscopy, FE-SEM, TEM, and XPS. In addition, the as-prepared Cr<sub>2</sub>CT<sub>x</sub> MXene was used as a catalyst support for the synthesis of eugenol-1,2,3-triazole via azide-alkyne cycloaddition reaction. Optimal reaction conditions, utilizing 10 wt% Cr<sub>2</sub>CT<sub>x</sub> MXene at 80 °C for 17 h, resulted in a 33 % yield, where both intermediate compounds and the final product were comprehensively characterized by FTIR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, and LC-MS/MS. Besides, Cr<sub>2</sub>CT<sub>x</sub> MXene catalyst was successfully reused for up to three cycles, demonstrating excellent durability and maintaining high product yields without significant loss of activity. Furthermore, the synthesized eugenol-1,2,3-triazole exhibited significant antioxidant activity in the DPPH assay, with 80 % radical scavenging at a concentration of 1000 μg/mL. This finding offers novel insights into the catalytic potential of Cr<sub>2</sub>CT<sub>x</sub> MXene for efficient organic transformations, yielding compounds with promising antioxidant properties.</div></div>","PeriodicalId":13609,"journal":{"name":"Inorganic Chemistry Communications","volume":"182 ","pages":"Article 115537"},"PeriodicalIF":5.4000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387700325016545","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
The development of efficient heterogeneous catalysts for the synthesis of heterocyclic compounds is crucial for various applications. In this work, two-dimensional Cr2CTx MXene was successfully synthesized via a selective etching method using HF and HCl. Its formation and structural properties were comprehensively verified using various characterization techniques, including XRD, FTIR, Raman spectroscopy, FE-SEM, TEM, and XPS. In addition, the as-prepared Cr2CTx MXene was used as a catalyst support for the synthesis of eugenol-1,2,3-triazole via azide-alkyne cycloaddition reaction. Optimal reaction conditions, utilizing 10 wt% Cr2CTx MXene at 80 °C for 17 h, resulted in a 33 % yield, where both intermediate compounds and the final product were comprehensively characterized by FTIR, 1H NMR, 13C NMR, and LC-MS/MS. Besides, Cr2CTx MXene catalyst was successfully reused for up to three cycles, demonstrating excellent durability and maintaining high product yields without significant loss of activity. Furthermore, the synthesized eugenol-1,2,3-triazole exhibited significant antioxidant activity in the DPPH assay, with 80 % radical scavenging at a concentration of 1000 μg/mL. This finding offers novel insights into the catalytic potential of Cr2CTx MXene for efficient organic transformations, yielding compounds with promising antioxidant properties.
期刊介绍:
Launched in January 1998, Inorganic Chemistry Communications is an international journal dedicated to the rapid publication of short communications in the major areas of inorganic, organometallic and supramolecular chemistry. Topics include synthetic and reaction chemistry, kinetics and mechanisms of reactions, bioinorganic chemistry, photochemistry and the use of metal and organometallic compounds in stoichiometric and catalytic synthesis or organic compounds.