This work describes the one-pot direct reductive amination of carbonyl compounds with nitroarenes promoted by a polymer supported palladium catalyst, in the presence of molecular hydrogen as the reductant. This methodology is applicable, with slight differences, to both aliphatic and aromatic aldehydes. The operational simplicity, the mild reaction conditions, the high yields and the good recyclability of the supported catalyst are major advantages of this method. TEM observations of the catalyst showed that the active species are palladium nanoparticles having a size distribution centered at 5 nm within the polymeric support. © 2011 Elsevier B.V.

One-pot synthesis of aniline derivatives from nitroarenes under mild conditions promoted by a recyclable polymer-supported palladium catalyst / Dell'Anna, M.M., Mastrorilli, P., Rizzuti, A., Leonelli, C.. - In: APPLIED CATALYSIS A: GENERAL. - ISSN 0926-860X. - ELETTRONICO. - 401:1-2(2011), pp. 134-140. [10.1016/j.apcata.2011.05.010]

One-pot synthesis of aniline derivatives from nitroarenes under mild conditions promoted by a recyclable polymer-supported palladium catalyst

RIZZUTI, Antonino;LEONELLI, Cristina
2011

Abstract

This work describes the one-pot direct reductive amination of carbonyl compounds with nitroarenes promoted by a polymer supported palladium catalyst, in the presence of molecular hydrogen as the reductant. This methodology is applicable, with slight differences, to both aliphatic and aromatic aldehydes. The operational simplicity, the mild reaction conditions, the high yields and the good recyclability of the supported catalyst are major advantages of this method. TEM observations of the catalyst showed that the active species are palladium nanoparticles having a size distribution centered at 5 nm within the polymeric support. © 2011 Elsevier B.V.
2011
no
Inglese
401
1-2
134
140
http://www.sciencedirect.com/science/article/pii/S0926860X11002870
One-pot reductive amination; Palladium nanoparticles; Supported catalysis; TEM; Catalysis; Process Chemistry and Technology
The manuscript presents the results of a fruitful informal research collaboration between the Dipartimento d’Ingegneria delle Acque e di Chimica del Politecnico di Bari, Bari, Italy and Dipartimento d’Ingegneria dei Materiali e dell’Ambiente, Università di Modena e Reggio Emilia, Modena, Italy. The results of this study represent an important step forward in the direction of "green chemistry" synthetic procedures for organic compoinds preparation.
reserved
info:eu-repo/semantics/article
Contributo su RIVISTA::Articolo su rivista
262
One-pot synthesis of aniline derivatives from nitroarenes under mild conditions promoted by a recyclable polymer-supported palladium catalyst / Dell'Anna, M.M., Mastrorilli, P., Rizzuti, A., Leonelli, C.. - In: APPLIED CATALYSIS A: GENERAL. - ISSN 0926-860X. - ELETTRONICO. - 401:1-2(2011), pp. 134-140. [10.1016/j.apcata.2011.05.010]
Dell'Anna, Maria Michela; Mastrorilli, Piero; Rizzuti, Antonino; Leonelli, Cristina
4
   Collaborazione informale fra Dipartimento d’Ingegneria delle Acque e di Chimica del Politecnico di Bari, Bari, Italy e Dipartimento d’Ingegneria dei Materiali e dell’Ambiente, Università di Modena e Reggio Emilia, Modena, Italy
File in questo prodotto:
File Dimensione Formato  
J Catalyst A 2011.pdf

Accesso riservato

Descrizione: Articolo pubblicato
Tipologia: VOR - Versione pubblicata dall'editore
Dimensione 822.19 kB
Formato Adobe PDF
822.19 kB 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/11380/1107274
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 58
  • ???jsp.display-item.citation.isi??? 56
social impact