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dc.contributor.authorMerinero, Alba D.-
dc.contributor.authorCollado, Alba-
dc.contributor.authorCasarrubios, Luis-
dc.contributor.authorGómez Gallego, Mar-
dc.contributor.authorRamírez de Arellano, Carmen-
dc.contributor.authorCaballero, Antonio-
dc.contributor.authorZapata Fernández, Fabiola-
dc.contributor.authorSierra, Miguel A.-
dc.contributor.otherFacultades, Departamentos, Servicios y Escuelas::Departamentos de la UMU:: Química Orgánicaes
dc.date.accessioned2024-02-07T08:51:38Z-
dc.date.available2024-02-07T08:51:38Z-
dc.date.issued2019-12-02-
dc.identifier.citationInorganic Chemistry 58 (23), 2019:16267−16278es
dc.identifier.issnPrint: 0020-1669-
dc.identifier.issnElectronic: 1520-510X-
dc.identifier.urihttp://hdl.handle.net/10201/138825-
dc.description©2019. This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ This document is the Accepted, version of a Published Work that appeared in final form in Inorganic Chemistry. To access the final edited and published work see https://doi.org/10.1021/acs.inorgchem.9b02813-
dc.description.abstractThrough a Cu-catalyzed Huisgen cycloaddition between terminal alkynes and azides (CuAAC) reaction, azide [(μ-SCH2)2N(4- N3C6H4)Fe2(CO)6] has demonstrated to be a robust and versatile reagent able to incorporate the [(μ-SR)2Fe2(CO)6] fragment on a wide range of substrates, ranging from aromatic compounds to nucleosides, metallocenes, or redox and luminescent markers. The [FeIFeI]/[Fe0FeI] and [Fe0FeI]/[Fe0Fe0] reduction potentials of the triazole derivatives prepared are comparable to those of other aminodithiolate (adt) Fe−Fe hydrogenase mimics. The presence of the triazole linker influences the electrochemical behavior of these complexes depending on the strength of the acid employed.es
dc.formatapplication/pdfes
dc.format.extent12es
dc.languageenges
dc.publisherAmerican Chemical Societyes
dc.relationCTQ2016-77555-C2-1-R and CTQ2016-81797-REDC (Programa Redes Consolider) from the MINECO (Spain) and from Fundación Ramón Areces (CIVP18A3938)es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NoCommercial-NoDerivatives 4.0 Internacional-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectTriazolees
dc.subjectHydrogenase Mimics-
dc.subjectElectrocatalytic-
dc.subject.otherCDU::5 - Ciencias puras y naturales::54 - Química::547 - Química orgánicaes
dc.titleTriazole-Containing [FeFe] Hydrogenase Mimics: Synthesis and Electrocatalytic Behaviores
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.1021/acs.inorgchem.9b02813-
Aparece en las colecciones:Artículos: Química Orgánica

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