Please use this identifier to cite or link to this item:
http://hdl.handle.net/2307/274
Title: | Palladium nanoparticles supported on polyvinylpyridine: Catalyticactivity in Heck-type reactions and XPS structural studies | Authors: | Evangelisti, Claudio Panziera, Nicoletta Pertici, Paolo Vitulli, Giovanni Salvadori, Piero Battocchio, Chiara Polzonetti, Giovanni |
Keywords: | cross-coupling reactions ray photoelectron-spectroscopy heterogeneous CATALYSTS metal-catalysts PD |
Issue Date: | Mar-2009 | Publisher: | Elsevier | Abstract: | Palladium nanoparticles, obtained by metal vapour synthesis (MVS), weredeposited on cross-linked polyvinylpyridine. The Pd/PVPy system showedhigh catalytic activity in the Heck C-C coupling reaction of iodo- andbromo-arenes (iodobenzene, bromobenzene, p-nitrobromobenzene,p-bromoacetophenone, p-(methoxy)bromobenzene) with alkyl acrylates(methyl acrylate, n-butyl acrylate, ethylhexyltrans-3-(4-methoxyphenyl)acrylate) at 100 degrees C-175 degrees Cworking under nitrogen atmosphere as well as in air. The catalyst isstable and the leaching of metal in solution is very low. When reused,the recovered Pd/PVPy maintains the catalytic activity of the pristinematerial. XPS structural studies performed on the starting catalyst aswell as on the recovered one indicate the presence of a interactionbetween the basic nitrogen of the pyridine present in the polymer andthe metal. (C) 2009 Elsevier Inc. All rights reserved. | URI: | http://hdl.handle.net/2307/274 | ISSN: | 0021-9517 | DOI: | 10.1016/j.jcat.2009.01.005 |
Appears in Collections: | A - Articolo su rivista X_Dipartimento di Fisica 'Edoardo Amaldi' |
Files in This Item:
File | Description | Size | Format | Existing users please Login |
---|---|---|---|---|
JCat.pdf | 230.69 kB | Adobe PDF | Request a copy |
Page view(s)
114
Last Week
0
0
Last month
1
1
checked on Nov 21, 2024
Download(s)
14
checked on Nov 21, 2024
Google ScholarTM
Check
Altmetric
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.