NH2- or PPh2-functionalized linkers for the immobilization of palladium on magnetite nanoparticles?

Immobilization of palladium on magnetite nanoparticles has been carried out with the assistance of two differently functionalized linkers containing phosphino-or amino-terminated groups. The linkers have been anchored to the magnetite surface by means of catechol, mercapto or carboxylate groups. The...

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Detalles Bibliográficos
Autores: Caparrós Rodríguez, Francisco Javier, Guarnizo Franco, Anderson, Rossell, Marta Dàcil, Angurell Purroy, Inmaculada, Seco, Miquel (Seco García), Müller Jevenois, Guillermo, Llorca, Jordi, 1966-, Rossell Alfonso, Oriol
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/128144
Acceso en línea:https://hdl.handle.net/2445/128144
Access Level:acceso abierto
Palabra clave:Pal·ladi (Element químic)
Magnetita
Nanopartícules
Catàlisi
Palladium
Magnetite
Nanoparticles
Catalysis
Descripción
Sumario:Immobilization of palladium on magnetite nanoparticles has been carried out with the assistance of two differently functionalized linkers containing phosphino-or amino-terminated groups. The linkers have been anchored to the magnetite surface by means of catechol, mercapto or carboxylate groups. The nature of the resulting Pd nanoparticles deposited has been examined by HAADF-STEM images and XPS electron spectroscopy. The efficiency of the two kinds of catalysts has been checked and compared for the Suzuki-Miyaura reaction, 4-nitrophenol reduction and styrene hydrogenation. The results evidence that the nanoparticles equipped with the phosphino fragment are better catalysts than those functionalized with the amino group and, in some processes, they are among the most active catalysts reported in the literature.