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Magnetically Separable Visible Light-Active Ag(0.75)Ni(0.25) Binary Alloy Nanoparticles as a Highly Efficient Photocatalyst for the Selective Oxidative Coupling of Aniline to Azobenzene

[Image: see text] Aniline wastes can be converted to useful pharmaceutical and industrial compounds like azobenzene. For this purpose, a bimetallic Ag(0.75)Ni(0.25) alloy is designed in the nanoscale range resembling a fivefold twinned morphology using water as the solvent. These newly developed all...

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Detalles Bibliográficos
Autores principales: Agarwal, Soniya, Dowara, Bidisa, Kumar, Sanjeev, Kumar, Vinod, Deori, Kalyanjyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798513/
https://www.ncbi.nlm.nih.gov/pubmed/36591159
http://dx.doi.org/10.1021/acsomega.2c07441
Descripción
Sumario:[Image: see text] Aniline wastes can be converted to useful pharmaceutical and industrial compounds like azobenzene. For this purpose, a bimetallic Ag(0.75)Ni(0.25) alloy is designed in the nanoscale range resembling a fivefold twinned morphology using water as the solvent. These newly developed alloy nanoparticles (NPs) are employed for the first time as an efficient visible light-active photocatalyst for the oxidative homocoupling of aniline to azobenzene. Our catalytic protocol is highly sustainable for a large number of aniline substrates with a high yield of the product (up to 95%), which might be attributed to the combinational and superior properties achieved on alloy formation in comparison to the monometallic counterparts. High-electron density amines (p-anisidine) display greater photocatalytic proficiency than that of low-electron density amines (4-fluoroaniline). The developed photocatalyst is magnetically well-separable and can be reused for at least five catalytic cycles without appreciable loss in its activity.