Polymer supported palladium nanoparticles, generated in situ by Pd(II) reduction under reaction conditions, catalyzed the hydrogenation of nitroarenes to anilines with high efficiency in water at room temperature in the presence of NaBH4. The protocol proved to be highly selective and generally favored the formation of the desired aniline as single product in high yields with short reaction times. TEM analyses revealed that the size distribution of the formed Pd nanocrystals was regulated by the reductant agent. In details, when 1 atm H2 was used as the nitroarene reductant, the in situ generated polymer supported palladium nanoparticles were crystallites with diameters ranging from 6 to 10 nm. On the contrary, when the reaction was carried out in the presence of NaBH4 in water under N2 or air, the formation of Pd nanocrystallites was observed as well, but this time they were smaller (mean size diameter ca. 3 nm) and catalytically more active compared to the palladium nanoparticles formed under 1 atm H2 in the absence of NaBH4. The catalyst displayed excellent recyclability over twelve cycles and no leaching of metal into solution occurred, which made the overall system eco-friendly and economic.

Polymer supported palladium nanocrystals as efficient and recyclable catalyst for the reduction of nitroarenes to anilines under mild conditions in water / Dell'Anna, M.M., Intini, S., Romanazzi, G., Rizzuti, A., Leonelli, C., Piccinni, F., Mastrorilli, P.. - In: JOURNAL OF MOLECULAR CATALYSIS. A: CHEMICAL. - ISSN 1381-1169. - ELETTRONICO. - 395:(2014), pp. 307-314. [10.1016/j.molcata.2014.08.033]

Polymer supported palladium nanocrystals as efficient and recyclable catalyst for the reduction of nitroarenes to anilines under mild conditions in water

RIZZUTI, Antonino;LEONELLI, Cristina;
2014

Abstract

Polymer supported palladium nanoparticles, generated in situ by Pd(II) reduction under reaction conditions, catalyzed the hydrogenation of nitroarenes to anilines with high efficiency in water at room temperature in the presence of NaBH4. The protocol proved to be highly selective and generally favored the formation of the desired aniline as single product in high yields with short reaction times. TEM analyses revealed that the size distribution of the formed Pd nanocrystals was regulated by the reductant agent. In details, when 1 atm H2 was used as the nitroarene reductant, the in situ generated polymer supported palladium nanoparticles were crystallites with diameters ranging from 6 to 10 nm. On the contrary, when the reaction was carried out in the presence of NaBH4 in water under N2 or air, the formation of Pd nanocrystallites was observed as well, but this time they were smaller (mean size diameter ca. 3 nm) and catalytically more active compared to the palladium nanoparticles formed under 1 atm H2 in the absence of NaBH4. The catalyst displayed excellent recyclability over twelve cycles and no leaching of metal into solution occurred, which made the overall system eco-friendly and economic.
2014
no
Inglese
395
307
314
http://www.sciencedirect.com/science/article/pii/S1381116914003902
Nitrobenzene reduction; Palladium nanoparticles; Polymer supported catalyst; Water solvent; Catalysis; Physical and Theoretical Chemistry; Process Chemistry and Technology
The manuscript presents the results of the fruitful research collaboration between the DICATECh, Politecnico di Bari, Bari, Italy, and the Dipartimento d'Ingegneria Dei Materiali e dell'Ambiente, Università di Modena e Reggio Emilia, Modena, Italy. For this particular experimental study the Consiglio Nazionale delle Ricerche, Istituto di Chimica dei Composti Organometallici (CNR-ICCOM), Bari, Italy, was involved. 
reserved
info:eu-repo/semantics/article
Contributo su RIVISTA::Articolo su rivista
262
Polymer supported palladium nanocrystals as efficient and recyclable catalyst for the reduction of nitroarenes to anilines under mild conditions in water / Dell'Anna, M.M., Intini, S., Romanazzi, G., Rizzuti, A., Leonelli, C., Piccinni, F., Mastrorilli, P.. - In: JOURNAL OF MOLECULAR CATALYSIS. A: CHEMICAL. - ISSN 1381-1169. - ELETTRONICO. - 395:(2014), pp. 307-314. [10.1016/j.molcata.2014.08.033]
Dell'Anna, Maria Michela; Intini, Simona; Romanazzi, Giuseppe; Rizzuti, Antonino; Leonelli, Cristina; Piccinni, Ferruccio; Mastrorilli, Piero
7
   Informal reserach collaboration between DICATECh, Politecnico di Bari, Bari, Italy, and the Dipartimento d'Ingegneria Dei Materiali e dell'Ambiente, Università di Modena e Reggio Emilia, Modena, Italy
File in questo prodotto:
File Dimensione Formato  
j molecular catalyst 2014.pdf

Accesso riservato

Descrizione: Articolo pubblicato
Tipologia: VOR - Versione pubblicata dall'editore
Dimensione 1.26 MB
Formato Adobe PDF
1.26 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1107544
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 68
  • ???jsp.display-item.citation.isi??? 64
social impact