Sharma Aditi, Sharma Shivani, Dutta Sriparna, Yadav Sneha, Dixit Ranjana, Arora Bhavya, Mehta Shilpa, Srivastava Anju, Sharma Rakesh K
Green Chemistry Network Centre, Department of Chemistry, University of Delhi, New Delhi-110007, India.
Department of Chemistry, Ramjas College, University of, Delhi, Delhi-110007, India.
Dalton Trans. 2023 Aug 15;52(32):11303-11314. doi: 10.1039/d3dt01265d.
Two-dimensional (2D) graphene oxide nanosheets serve as an excellent support material for immobilizing metal complexes to deal with the drawbacks of homogeneous catalysis. In this work, we report a magnetically retrievable graphene oxide (MGO) based copper nanocatalytic system that has been efficiently exploited for obtaining a series of pharmaceutically and biologically active benzoxazole scaffolds. The nanocatalyst was designed by covalent immobilization of dehydroacetic acid (DHA) onto a magnetic amino-silanized graphene oxide nanosupport which was accompanied by its metallation with copper acetate. The structure of the synthesized MGO hybrid material (Cu@DHA@APTES@MGO) was characterized by numerous physico-chemical techniques such as transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), elemental mapping, atomic absorption spectroscopy (AAS), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET) surface area analysis and energy-dispersive X-ray fluorescence spectroscopy (ED-XRF). The fabricated architectures exhibited high efficiency for cyclization of 2-aminophenols and β-diketones with wide substrate scope, excellent functional group tolerance, a higher conversion percentage (>98%) and a high turnover number (TON). The exceptional catalytic activity could be attributed to the 2D architecture of graphene oxide which provides space for trapping of reactants between 2D graphitic overlayers and metal surfaces and the reaction proceeds to afford benzoxazole products with moderate to excellent conversion percentages. Notably, this nanocomposite could be recovered easily through an external magnetic force and reused for multiple runs without any appreciable loss in its catalytic efficacy.
二维(2D)氧化石墨烯纳米片作为一种优异的载体材料,用于固定金属配合物,以解决均相催化的缺点。在本工作中,我们报道了一种基于磁性可回收氧化石墨烯(MGO)的铜纳米催化体系,该体系已被有效地用于合成一系列具有药学和生物学活性的苯并恶唑支架。通过将脱氢乙酸(DHA)共价固定在磁性氨基硅烷化氧化石墨烯纳米载体上,并使其与乙酸铜金属化,设计了该纳米催化剂。通过多种物理化学技术对合成的MGO杂化材料(Cu@DHA@APTES@MGO)的结构进行了表征,如透射电子显微镜(TEM)、场发射扫描电子显微镜(FE-SEM)、傅里叶变换红外光谱(FT-IR)、X射线衍射(XRD)、振动样品磁强计(VSM)、元素映射、原子吸收光谱(AAS)、热重分析(TGA)、布鲁诺尔-埃米特-泰勒(BET)表面积分析和能量色散X射线荧光光谱(ED-XRF)。所构建的结构对2-氨基酚和β-二酮的环化反应表现出高效性,底物范围广,官能团耐受性好,转化率高(>98%)且周转数高(TON)。这种优异的催化活性可归因于氧化石墨烯的二维结构,它为反应物在二维石墨覆盖层和金属表面之间的捕获提供了空间,反应能够顺利进行,以中等至优异的转化率生成苯并恶唑产物。值得注意的是,这种纳米复合材料可以通过外部磁力轻松回收,并多次重复使用,而其催化效果没有明显损失。