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dc.contributor.authorGómez-Oliveira, Eloy P.
dc.contributor.authorCastells-Gil, Javier
dc.contributor.authorChinchilla-Garzón, Clara
dc.contributor.authorUscategui-Linares, Andrés
dc.contributor.authorAlbero, Josep
dc.contributor.authorAlmora-Barrios, Neyvis
dc.contributor.authorTatay, Sergio
dc.contributor.authorM. Padial, Natalia
dc.contributor.authorMartí-Gastaldo, Carlos
dc.date.accessioned2025-01-30T10:34:08Z
dc.date.available2025-01-30T10:34:08Z
dc.date.issued2024-11
dc.identifier.citationJ. Am. Chem. Soc. 2024, 146, 31021–31033.es_ES
dc.identifier.urihttps://hdl.handle.net/10481/101243
dc.descriptionSubmitted versiones_ES
dc.description.abstractThe increasing use of Metal-Organic Frameworks (MOFs) in separation, catalysis or storage is linked to the targeted modification of their composition or porosity metrics. While modification of pore shape and size necessarily implies the assembly of alternative nets, compositional changes often rely on post-synthetic modification adapted to the functionalisation or exchange of the organic linker, or the modification of the inorganic cluster by metal exchange methods. We describe an alternative methodology that enables the integration of both types of modification, structural and compositional, in titanium MOFs by metal exchange reaction of the heterometallic cluster Ti2 Ca2 . A systematic analysis of this reactivity with MUV-10 is used to understand which experimental variables are crucial to enable replacement of calcium only, or to integrate metal exchange with structural transformation. The isoreticular expanded framework MUV-30, is next used to template the formation of MUV-301, a titanium framework not accessible by direct synthesis that displays the largest mesoporous cages reported to date. Given that the interest of Ti MOFs in photoredox applications often meets the limitations imposed by the challenges of titanium solution chemistry to design concrete candidates, this soft strategy based on pre-assembled frameworks will help integrating specific combinations of metals into high porosity architectures.es_ES
dc.description.sponsorshipThis work was supported by the H2020 program (ERC-2021-COG- 101043428), Generalitat Valenciana (PROMETEU/2021/054, MFA/2022/026, and SEJIGENT/2021/059), and Spanish govern- ment (CEX2019-000919-M, CNS2022-135677, PID2020118117RB-I00). C.C.-G. thanks the Spanish government for the FPI grant (PRE2021-098634). J.C.-G. thanks Generalitat Valen- ciana for the APOSTD fellowship (CIAPOS/2021/272). N.M.P. thanks the La Caixa Foundation for a Postdoctoral Junior Leader– Retaining Fellowship (ID 100010434, fellowship code LCF/BQ/PR20/11770014). We also thank the University of Valen- cia for their research facilities (NANBIOSIS) and the Synchotron ALBA for the access to synchrotron radiation at beamlines XALOC (proposal 2022086946) and MSPD (2021035124).es_ES
dc.language.isoenges_ES
dc.publisherAMERICAN CHEMICAL SOCIETY, USA.es_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.titleIntegrating Compositional and Structural Diversity in Heterometallic Titanium Frameworks by Metal Exchange Methods.es_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1021/jacs.4c10444
dc.type.hasVersionAOes_ES


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