Multifunctional catalysts based on palladium nanoparticles supported on functionalized halloysites: Applications in catalytic C-C coupling, selective oxidation and dehalogenation reactions

dc.affiliation.dptoBiología y Geología, Física y Química Inorgánica
dc.contributor.authorDíaz-Sánchez, Miguel
dc.contributor.authorGómez, I. Jénnifer
dc.contributor.authorPrashar, Sanjiv
dc.contributor.authorHoráček, Michal
dc.contributor.authorLamač, Martin
dc.contributor.authorUrbán, Béla
dc.contributor.authorPinkas, Jiří
dc.contributor.authorGómez-Ruiz, Santiago
dc.contributor.funderMinisterio de Ciencia e Innovación of Spain
dc.contributor.funderDirección General de Investigación e Innovación, Consejería de Educación e Investigación de la Comunidad de Madrid
dc.contributor.funderUniversidad Rey Juan Carlos
dc.contributor.funderBanco de Santander
dc.date.accessioned2025-12-15T08:12:39Z
dc.date.issued2021-11
dc.description.abstractA series of hybrid catalysts of the type, support-ligand-Pd (Sup-L-Pd), has been prepared and characterized and their activity in C-C coupling (Suzuki-Miyaura), selective oxidations and dehalogenation‑hydrogenation processes studied. The hybrid Sup-L-Pd catalysts are made up of (i) different nano-sized supports, such as halloysite nanotubes (HNTs), SiO2, Al2O3 and mesoporous silica nanoparticles (MSNs), (ii) ligands (L) with N-, S- or P-donor atoms and (iii) different quantities of Pd. Several combinations of support, ligand, and Pd quantity were used to determine the optimal composition of the nanostructured systems for the proposed catalytic reactions. The system based on HNTs functionalized with 2-(diphenylphosphino)ethyltriethoxysilane (PPETS) and 0.25% wt. Pd (HNTs-PPETS-Pd0.25) showed the most promising catalytic behaviour with multifunctional applicability in different catalytic processes and potential reusability. This catalyst gave turnover frequency (TOF) values of up to 155 h−1 in catalytic Suzuki-Miyaura C-C coupling reactions, up to 43 h−1 in selective catalytic oxidations and up to 65 h−1 in dehalogenation‑hydrogenation processes of halogenated aromatic compounds. Furthermore, the system demonstrated in the different catalytic reactions, good recyclability after consecutive cycles with low Pd leaching.
dc.description.sponsorshipMinisterio de Ciencia e Innovación of Spain (formerly Ministerio de Ciencia Innovación y Universidades of Spain), grant number RTI2018-094322-B-I00 Dirección General de Investigación e Innovación, Consejería de Educación e Investigación de la Comunidad de Madrid for the predoctoral grant PEJD-2017-PRE/AMB-4047 (M. D.-S.). Universidad Rey Juan Carlos (International School of Doctoral Studies) and Banco de Santander are gratefully acknowledged for the mobility scholarship to obtain International Doctor mention BDNS (496679).
dc.identifier.citationMiguel Díaz-Sánchez, I. Jénnifer Gómez, Sanjiv Prashar, Michal Horáček, Martin Lamač, Béla Urbán, Jiří Pinkas, Santiago Gómez-Ruiz, Multifunctional catalysts based on palladium nanoparticles supported on functionalized halloysites: Applications in catalytic C-C coupling, selective oxidation and dehalogenation reactions, Applied Clay Science, Volume 214, 2021, 106272, ISSN 0169-1317, https://doi.org/10.1016/j.clay.2021.106272.
dc.identifier.doi10.1016/j.clay.2021.106272
dc.identifier.publicationfirstpage1
dc.identifier.publicationissue106272
dc.identifier.publicationlastpage11
dc.identifier.publicationtitleApplied Clay Science
dc.identifier.publicationvolume214
dc.identifier.urihttps://hdl.handle.net/10115/129937
dc.language.isoen
dc.publisherElsevier
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectcatalysis
dc.subjectpalladium
dc.subjectnanoclays
dc.subjecthalloysite nanotubes
dc.subjectalumina
dc.subjectsilica
dc.subjectnanocatalysis
dc.titleMultifunctional catalysts based on palladium nanoparticles supported on functionalized halloysites: Applications in catalytic C-C coupling, selective oxidation and dehalogenation reactions
dc.typeArticle
dc.type.hasVersionhttp://purl.org/coar/version/c_ab4af688f83e57aa

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