New hybrid materials based on the grafting of Pd(II)-amino complexes on the graphitic surface of AC: preparation, structures and catalytic properties

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Title: New hybrid materials based on the grafting of Pd(II)-amino complexes on the graphitic surface of AC: preparation, structures and catalytic properties
Authors: Godino-Salido, M. Luz | Gutiérrez-Valero, María D. | López-Garzón, Rafael | Arranz-Mascarós, Paloma | Santiago-Medina, Antonio | Melguizo-Guijarro, Manuel | Domingo-García, María | López-Garzón, F. Javier | Abdelkader-Fernández, Victor K. | Salinas Martínez de Lecea, Concepción | Román-Martínez, M. Carmen
Research Group/s: Materiales Carbonosos y Medio Ambiente
Center, Department or Service: Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Materiales
Keywords: Hybrid materials | Grafting | Pd(II)-amino complexes | Graphitic surface | AC
Knowledge Area: Química Inorgánica
Issue Date: 7-Jun-2016
Publisher: Royal Society of Chemistry
Citation: RSC Advances. 2016, 6: 58247-58259. doi:10.1039/C6RA08858A
Abstract: A novel procedure for the preparation of solid Pd(II)-based catalysts consisting of the anchorage of designed Pd(II)-complexes on an activated carbon (AC) surface is reported. Two molecules of the Ar–S–F type (where Ar is a plane-pyrimidine moiety, F a Pd(II)-ligand and S an aliphatic linker) differing in F, were grafted on AC by π–π stacking of the Ar moiety and the graphene planes of the AC, thus favouring the retaining of the metal-complexing ability of F. Adsorption of Pd(II) by the AC/Ar–S–F hybrids occurs via Pd(II)-complexation by F. After deep characterization, the catalytic activities of the AC/Ar–S–F/Pd(II) hybrids on the hydrogenation of 1-octene in methanol as a catalytic test were evaluated. 100% conversion to n-octane at T = 323.1 K and P = 15 bar, was obtained with both catalysts and most of Pd(II) was reduced to Pd(0) nanoparticles, which remained on the AC surface. Reusing the catalysts in three additional cycles reveals that the catalyst bearing the F ligand with a larger Pd-complexing ability showed no loss of activity (100% conversion to n-octane) which is assigned to its larger structural stability. The catalyst with the weaker F ligand underwent a progressive loss of activity (from 100% to 79% in four cycles), due to the constant aggregation of the Pd(0) nanoparticles. Milder conditions, T = 303.1 K and P = 1.5 bar, prevent the aggregation of the Pd(0) nanoparticles in this catalyst allowing the retention of the high catalytic efficiency (100% conversion) in four reaction cycles.
Sponsor: The supports of the MINECO (projects MAT2014-60104-C2-1-R, MAT2014-60104-C2-2-R and CTM2010-16770), the Autonomous Regional Government (J. de Andalucía, Groups PAIDI FQM273 and RNM342), the Programa de Fortalecimiento de la I+D+I from UGR and Feder funds and the University of Jaén (Project UJA2014/02_FT/06 corresponding to the PROGRAMA OPERATIVO FEDER ANDALUCÍA) are acknowledged.
URI: http://hdl.handle.net/10045/56122
ISSN: 2046-2069
DOI: 10.1039/C6RA08858A
Language: eng
Type: info:eu-repo/semantics/article
Rights: © The Royal Society of Chemistry 2016
Peer Review: si
Publisher version: http://dx.doi.org/10.1039/C6RA08858A
Appears in Collections:INV - MCMA - Artículos de Revistas

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