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dc.contributor.authorCorral, Jorge A.
dc.contributor.authorLópez, María I.
dc.contributor.authorEsquivel, Dolores
dc.contributor.authorMora, Manuel
dc.contributor.authorJiménez-Sanchidrián, César
dc.contributor.authorRomero-Salguero, F.J.
dc.date.accessioned2017-11-09T12:22:41Z
dc.date.available2017-11-09T12:22:41Z
dc.date.issued2013
dc.identifier.urihttp://hdl.handle.net/10396/15399
dc.description.abstractThree periodic mesoporous materials, i.e., two organosilicas with either ethylene or phenylene bridges and one silica, have been used as supports for Pd nanoparticles. All Pd-supported samples (1.0 wt%) were prepared by the incipient wetness method and subsequently reduced in an H2 stream at 200 °C. Both hydrogen chemisorption and temperature programmed reduction experiments revealed significant differences depending on the support. Pd2+ species were more reducible on the mesoporous organosilicas than on their silica counterpart. Also, remarkable differences on the particle morphology were observed by transmission electron microscopy. All Pd-supported samples were active in the Suzuki cross-coupling reaction between bromobenzene and phenylboronic acides_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightshttps://creativecommons.org/licenses/by/4.0/es_ES
dc.sourceMaterials 6(4), 1554-1565 (2013)es_ES
dc.subjectPeriodic mesoporous organosilicaes_ES
dc.subjectPalladium nanoparticleses_ES
dc.subjectHydrogen chemisorptiones_ES
dc.subjectTemperature programmed reductiones_ES
dc.subjectPd-supported catalystses_ES
dc.subjectSuzuki cross-couplinges_ES
dc.titlePreparation of Palladium-Supported Periodic Mesoporous Organosilicas and their Use as Catalysts in the Suzuki Cross-Coupling Reactiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttp://dx.doi.org/10.3390/ma6041554es_ES
dc.relation.projectIDGobierno de España. MAT2010-18778es_ES
dc.relation.projectIDJunta de Andalucía. FQM-346es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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