Polymer supported nickel nanoparticles, generated by calcination under nitrogen of a Ni(II) containing polyacrylamide, catalyzed the hydrogenation of nitroarenes to anilines in aqueous medium at room temperature in the presence of NaBH4. The protocol generally favored the formation of the desired aniline as single product in high yields with short reaction times and proved to be highly selective in the hydrogenation of halonitrobenzene to haloaniline, avoiding the formation of hydro-dehalogenated side-products. The catalyst displayed excellent recyclability over at least five cycles (which is not trivial for nickel nanoparticle based catalysts used in water) and no leaching of metal into solution occurred, that made the overall system eco-friendly and economic. STEM analyses revealed that the thermally formed Ni nanoparticles turned into cubic nanotwins under reaction conditions, which remained almost unchanged with the re-cycles.

Polymer supported Nickel nanoparticles as recyclable catalyst for the reduction of nitroarenes to anilines in aqueous medium

Fiore, Ambra Maria;Nacci, Angelo;
2018-01-01

Abstract

Polymer supported nickel nanoparticles, generated by calcination under nitrogen of a Ni(II) containing polyacrylamide, catalyzed the hydrogenation of nitroarenes to anilines in aqueous medium at room temperature in the presence of NaBH4. The protocol generally favored the formation of the desired aniline as single product in high yields with short reaction times and proved to be highly selective in the hydrogenation of halonitrobenzene to haloaniline, avoiding the formation of hydro-dehalogenated side-products. The catalyst displayed excellent recyclability over at least five cycles (which is not trivial for nickel nanoparticle based catalysts used in water) and no leaching of metal into solution occurred, that made the overall system eco-friendly and economic. STEM analyses revealed that the thermally formed Ni nanoparticles turned into cubic nanotwins under reaction conditions, which remained almost unchanged with the re-cycles.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/209110
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