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Polymer-coated palladium nanoparticle catalysts for Suzuki coupling reactions.
Bortolotto, Tanize; Facchinetto, Sara Elisa; Trindade, Suelen Gauna; Ossig, Andreia; Petzhold, Cesar Liberato; Vargas, Josimar; Rodrigues, Oscar Endrigo Dorneles; Giacomelli, Cristiano; Schmidt, Vanessa.
Afiliação
  • Bortolotto T; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • Facchinetto SE; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • Trindade SG; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • Ossig A; Instituto de Química, Universidade Federal do Rio Grande do Sul, 91501-970 Porto Alegre, RS, Brazil.
  • Petzhold CL; Instituto de Química, Universidade Federal do Rio Grande do Sul, 91501-970 Porto Alegre, RS, Brazil.
  • Vargas J; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • Rodrigues OE; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • Giacomelli C; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • Schmidt V; Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil. Electronic address: vschmidt@ufsm.br.
J Colloid Interface Sci ; 439: 154-61, 2015 Feb 01.
Article em En | MEDLINE | ID: mdl-25463188
ABSTRACT
A set of seven different palladium nanoparticle (PdNP) systems stabilized by small amounts (1.0mg/mL) of structurally related macromolecular capping agents were comparatively tested as catalyst in p-nitrophenol (Nip) reduction and Suzuki cross-coupling reactions. The observed rate constants (kobs) for Nip reduction were in the range of 0.052-3.120×10(-2)s(-1), and the variation reflected the effects of polymer chain conformation, ionic strength and palladium-polymer complex coordination. Macromolecules featuring pendant pyridyl moieties or inverse temperature-dependent solubility were found to be unsuitable capping agents for PdNPs catalysts, despite being active. The catalytic activity in Suzuki cross-coupling reactions followed the same behavior; the most active particles in the Nip reaction also mediated the cross-coupling reaction providing the expected products in quantitative yields under relatively mild conditions after only 4h at 50°C. Experiments involving the successive addition of reactants and catalyst recovery/re-use indicated that the recycling potential was comparable to those of the standards used in this field.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article