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dc.contributor.authorSarasola Iñiguez, Ane
dc.contributor.authorBarragán Durán, Ana Isabel
dc.contributor.authorVitali, Lucia
dc.date.accessioned2024-02-09T14:03:22Z
dc.date.available2024-02-09T14:03:22Z
dc.date.issued2018-11-21
dc.identifier.citationJournal of the American Chemical Society 140(46) : 15631-15634 (2018)
dc.identifier.issn0002-7863
dc.identifier.urihttp://hdl.handle.net/10810/65937
dc.description.abstractCopper is the paradigmatic catalyzer of the Ullmann cross-coupling reaction. Despite this, its role in the reaction is still under debate. Here, we shed light on the mechanistic steps of debromination, characterizing a prototypical molecule, namely 4,7-dibromobenzo[c]-1,2,5-thiadiazole (2Br-BTD), deposited on a Cu(110) surface. By means of scanning probe techniques and first principle calculations, we demonstrate the oxidative addition of Cu atoms leading to a −C–Cu–Br metal–organic complex. The scission of the strongly bound bromine atoms requires the cooperative action of neighboring complexes resulting in the formation of Cu-coordinated BTD structures.
dc.language.isoenges_ES
dc.publisherACS
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.titleCooperative Action for Molecular Debromination Reaction on Cu(110)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2018 American Chemical Society
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/jacs.8b10329
dc.identifier.doi10.1021/jacs.8b10329
dc.departamentoesFísica Aplicada I
dc.departamentoeuFisika Aplikatua I
dc.identifier.eissn1520-5126


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