4.6 Article

Zirconium phosphate supported-silver nanoparticles for selective hydrogenation of nitrobenzene into azoxybenzene compounds

Journal

NEW JOURNAL OF CHEMISTRY
Volume 47, Issue 30, Pages 14380-14394

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3nj00518f

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In this study, zirconium phosphate-supported silver nanoparticle catalysts were prepared and characterized. The catalysts showed a strong coordination interaction between silver nanoparticles and the phosphate group on zirconium phosphate, and the acidic sites on zirconium phosphate played a critical role in adsorbing nitrobenzene and activating NaBH4 for hydrogen transfer. The catalysts exhibited high activity and selectivity for the hydrogenation of substituted nitroarenes to azoxybenzene compounds, with full conversion of nitrobenzene achieved within 3 minutes and without leaching of silver species even after multiple recycling. Methanol was found to be an excellent solvent and hydrogen source in this reaction. Overall, the zirconium phosphate-supported silver nanoparticle catalysts are highly effective for selective hydrogenation of nitrobenzene to azoxybenzene compounds.
In this work, zirconium phosphate (ZrP) supported Ag nanoparticle (NP) catalysts were constructed. The as-obtained catalysts were characterized thoroughly by XRD, HAADF-STEM, py-IR spectroscopy, etc. A coordination interaction was found between Ag NPs and the phosphate group on ZrP, and the acidic sites on ZrP played a very critical role not only in adsorbing nitrobenzene, but also in activating NaBH4 to facilitate hydrogen transfer to Ag sites. It was indicated that the ZrP-supported Ag NP catalysts were highly active for catalytically selective hydrogenation of the substituted nitroarenes into azoxybenzene compounds by using NaBH4 as a hydrogen source. Notably, the catalysts could afford a full conversion of nitrobenzene within 3 min and an exceptional selectivity to azoxybenzene. Moreover, 1%Ag/ZrP-R was recycled eight times without obvious loss of activity. No leaching of Ag species was observed in consecutive catalytic cycles. Methanol was found to be a superior solvent for this reaction and also acted as a hydrogen resource in the reaction. On the basis of the catalytic activity test and density functional theory (DFT) calculations, the reaction pathway was proposed as well. To our knowledge, the ZrP-supported metal catalysts are some of the best catalyst systems for selective hydrogenation of nitrobenzene into azoxybenzene compounds with exceptional activity and selectivity.

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