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dc.contributor.author | Oliver-Meseguer, Judit | es_ES |
dc.contributor.author | Boronat Zaragoza, Mercedes | es_ES |
dc.contributor.author | Vidal Moya, José Alejandro | es_ES |
dc.contributor.author | Concepción Heydorn, Patricia | es_ES |
dc.contributor.author | Rivero-Crespo, Miguel Ángel | es_ES |
dc.contributor.author | Leyva Perez, Antonio | es_ES |
dc.contributor.author | Corma Canós, Avelino | es_ES |
dc.date.accessioned | 2020-11-07T04:32:39Z | |
dc.date.available | 2020-11-07T04:32:39Z | |
dc.date.issued | 2018-03-07 | es_ES |
dc.identifier.issn | 0002-7863 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/154389 | |
dc.description.abstract | [EN] The reactive nature of carbenes can be modulated, and ultimately reversed, by receiving additional electron density from a metal. Here, it is shown that Au nanoparticles (NPs) generate an electron-rich carbene on surface after transferring electron density to the carbonyl group of an in situ activated diazoacetate, as assessed by Fourier transformed infrared (FT¿IR) spectroscopy, magic angle spinning nuclear magnetic resonance (MAS NMR), and Raman spectroscopy. Density functional theory (DFT) calculations support the observed experimental values and unveil the participation of at least three different Au atoms during carbene stabilization. The surface stabilized carbene shows an extraordinary stability against nucleophiles and reacts with electrophiles to give new products. These findings showcase the ability of catalytic Au NPs to inject electron density in energetically high but symmetrically allowed valence orbitals of sluggish molecules. | es_ES |
dc.description.sponsorship | Financial support by MINECO through the Severo Ochoa program, RETOS program (CTQ2014-55178-R), and Ramon y Cajal Program (to A.L.-P.) is acknowledged. J.O.-M. thanks ITQ for the concession of a contract. We are thankful for the electron microscopy service of UPV. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | American Chemical Society | es_ES |
dc.relation.ispartof | Journal of the American Chemical Society | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject.classification | QUIMICA ANALITICA | es_ES |
dc.subject.classification | QUIMICA ORGANICA | es_ES |
dc.title | Generation and Reactivity of Electron-Rich Carbenes on the Surface of Catalytic Gold Nanoparticles | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1021/jacs.7b13696 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//CTQ2014-55178-R/ES/HIERRO Y BISMUTO SUB-NANOMETRICO Y CATALITICO/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Instituto Universitario Mixto de Tecnología Química - Institut Universitari Mixt de Tecnologia Química | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Química - Departament de Química | es_ES |
dc.description.bibliographicCitation | Oliver-Meseguer, J.; Boronat Zaragoza, M.; Vidal Moya, JA.; Concepción Heydorn, P.; Rivero-Crespo, MÁ.; Leyva Perez, A.; Corma Canós, A. (2018). Generation and Reactivity of Electron-Rich Carbenes on the Surface of Catalytic Gold Nanoparticles. Journal of the American Chemical Society. 140(9):3215-3218. https://doi.org/10.1021/jacs.7b13696 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1021/jacs.7b13696 | es_ES |
dc.description.upvformatpinicio | 3215 | es_ES |
dc.description.upvformatpfin | 3218 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 140 | es_ES |
dc.description.issue | 9 | es_ES |
dc.identifier.pmid | 29460623 | es_ES |
dc.relation.pasarela | S\358009 | es_ES |
dc.contributor.funder | Ministerio de Economía y Competitividad | es_ES |