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dc.contributor.authorPajuelo Corral, Oier
dc.contributor.authorPérez Yáñez, Sonia ORCID
dc.contributor.authorVitorica Yrezabal, Iñigo J.
dc.contributor.authorBeobide Pacheco, Garikoitz ORCID
dc.contributor.authorZabala Lekuona, Andoni
dc.contributor.authorRodríguez Diéguez, Antonio
dc.contributor.authorSeco Botana, José Manuel ORCID
dc.contributor.authorCepeda Ruiz, Javier
dc.date.accessioned2022-05-25T07:53:32Z
dc.date.available2022-05-25T07:53:32Z
dc.date.issued2022-06
dc.identifier.citationMaterials Today Chemistry 24 : (2022) // Article ID 100794es_ES
dc.identifier.issn2468-5194
dc.identifier.urihttp://hdl.handle.net/10810/56720
dc.description.abstract[EN] A versatile metal-organic system consisting of Co-based compounds that show reversible transformations between a 3D metal-organic framework (MOF) of {[Co(mu-3isoani)(2)]center dot DMF}(n) (1) formula (where 3isoani - 3-aminoisonicotinato and DMF - dimethylformamide) and a 0D monomeric [Co(3isoani)(2)(H2O)(4)] (2) complex is reported. These 1 <-> 2 transformations, triggered by the exposure of the MOF and the monomer-based compound to H2O and DMF, respectively, involve colour changes from purple (in MOF 1) to light brown (in monomeric complex 2), which imbues the system with colourimetric sensing capacity towards these solvents. Despite the high reactivity of the MOF in contact with water, it presents good thermal stability and permanent porosity with a remarkably high CO2 capture capacity at room temperature (3.35 mmol/g), which is further analysed by in situ single-crystal X-ray diffraction. Experimental magnetic properties and CASSCF/NEVPT2 calculations of all compounds reveal distinct slow magnetic relaxations for 3D and 0D compounds.es_ES
dc.description.sponsorshipThis work has been funded by the Spanish Ministry of Science, Innovation and Universities (MCIU/AEI/FEDER, UE; PGC2018-102052-A-C22, PGC2018-102052-B-C21 and PID2019-108028GBC21), University of the Basque Country (GIU20/028), Gobierno Vasco/Eusko Jaurlaritza (IT1005-16, IT1291-19) and Junta de Andalucia (FQM-394, B-FQM-734-UGR20). O.P.C. thanks his predoctoral fellowship to UPV/EHU. The authors thank for technical and human support provided by SGIker of UPV/EHU and European funding (ERDF and ESF).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/MICIU/PGC2018-102052-A-C22es_ES
dc.relationinfo:eu-repo/grantAgreement/MICIU/PGC2018-102052-B-C21es_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2019-108028GBC21es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectCO2 adsorptiones_ES
dc.subjectsolvent-triggered reversible transformationses_ES
dc.subjectcolorimetric sensinges_ES
dc.subjectsingle-molecule magnet behavioures_ES
dc.subjectMOFses_ES
dc.titleA metal-organic framework based on Co(II) and 3-aminoisonicotinate showing specific and reversible colourimetric response to solvent exchange with variable magnet behavioures_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S2468519422000234?via%3Dihubes_ES
dc.identifier.doi10.1016/j.mtchem.2022.100794
dc.departamentoesQuímica Orgánica e Inorgánicaes_ES
dc.departamentoesQuímica aplicadaes_ES
dc.departamentoeuKimika Organikoa eta Ez-Organikoaes_ES
dc.departamentoeuKimika aplikatuaes_ES


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© 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as © 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).