Two-dimensional vanadium carbide (V2CTx) MXenes for one-pot synthesis of 2,5-disubstituted-1,3,4-oxadiazoles†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY New Journal of Chemistry Pub Date : 2025-03-28 DOI:10.1039/D4NJ05159A
Sahana Raju, Yarabahally R. Girish, Mohd Sajid Ali, Hamad A. Al-Lohedan, K. Pramoda and Kothanahally S. Sharath Kumar
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Abstract

The development of new reusable and efficient heterogeneous catalysts for the construction of bioactive heterocyclic compounds is of great interest in the present era. Two-dimensional (2D) materials, especially 2D vanadium carbide (V2CTx MXene), are widely used in energy storage and conversion because of their good electronic properties and broad surface area, but 2D V2CTx MXene has not been explored as a catalyst support for organic transformation. Herein, we demonstrate a smooth cyclization reaction between aldehydes and hydrazides to construct 2,5-disubstituted-1,3,4-oxadiazoles catalyzed by 2D V2CTx MXenes. We were able to attach a wide range of substituents on the 2nd and 5th positions of the 1,3,4-oxadiazole ring. The present protocol showed broad functional group tolerance with product yields ranging from 84% to 93% in a shorter reaction time (30–45 min). The 2D V2CTx MXene catalyst was able to produce good yields of product even after five catalytic cycles.

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二维碳化钒(V2CTx) MXenes一锅法合成2,5-二取代-1,3,4-恶二唑†
开发新型可重复使用的高效多相催化剂用于构建具有生物活性的杂环化合物是当前研究的热点。二维(2D)材料,特别是二维碳化钒(V2CTx MXene)由于其良好的电子性能和广阔的表面积,在能量存储和转换中得到了广泛的应用,但二维V2CTx MXene作为有机转化的催化剂载体尚未被探索。在此,我们证明了在2D V2CTx MXenes催化下,醛和肼之间的平滑环化反应构建了2,5-二取代-1,3,4-恶二唑。我们可以在1,3,4-恶二唑环的第2和第5个位置上连接很多取代基。目前的方案显示出广泛的官能团耐受性,在较短的反应时间(30-45分钟)内,产品收率从84%到93%不等。2D V2CTx MXene催化剂在经过5次催化循环后仍能产生良好的产物收率。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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