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Catalytic Advantages of SO3H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel–Crafts Acylation Reaction

dc.contributor.authorBauza, Marta
dc.contributor.authorLeo, Pedro
dc.contributor.authorPalomino Cabello, Carlos
dc.contributor.authorMartín, Antonio
dc.contributor.authorOrcajo, Gisela
dc.contributor.authorTurnes Palomino, Gemma
dc.contributor.authorMartínez, Fernando
dc.date.accessioned2024-09-11T07:37:49Z
dc.date.available2024-09-11T07:37:49Z
dc.date.issued2024-09-03
dc.identifier.citationBauza, M., Leo, P., Palomino Cabello, C., Martin, A., Orcajo, G., Turnes Palomino, G., & Martinez, F. (2024). Catalytic Advantages of SO3H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel–Crafts Acylation Reaction. Inorganic Chemistry, 10.1021/acs.inorgchem.4c01792es
dc.identifier.issn0020-1669 (print)
dc.identifier.issn1520-510X (online)
dc.identifier.urihttps://hdl.handle.net/10115/39468
dc.description.abstractThe catalytic activity and stability of sulfonic-based UiO-66(Zr) materials were tested in the Friedel–Crafts acylation of anisole with acetic anhydride. The materials were prepared using microwave-assisted synthesis, producing microporous materials with remarkable crystallinity and physicochemical features as acid catalysts. Different ratios between both organic ligands, terephthalic acid (H2BDC) and monosodium 2-sulfoterephthalic acid (H2BDC–SO3Na), were used for the synthesis to modulate the sulfonic content. The sulfonic-based UiO-66(Zr) material synthesized with a H2BDC/H2BDC–SO3Na molar ratio of 40/60 exhibited the best catalytic performance in the acidic-catalyzed Friedel–Crafts acylation reaction. This ratio balanced the number of sulfonic acid sites and their accessibility within the UiO-66 microporous structure. The catalytic performance of this material increased remarkably at 200 °C, outperforming reference acids and commercial heterogeneous catalysts such as Nafion-SAC-13 and Amberlyst-70. Additionally, the best sulfonic-based UiO-66(Zr) material proved to be stable in four successive reaction cycles, maintaining both its catalytic activity and its structural integrityes
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCatalystses
dc.subjectChemical synthesises
dc.subjectMaterials Organic reactionses
dc.subjectPost-translational modificationes
dc.titleCatalytic Advantages of SO3H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel–Crafts Acylation Reactiones
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1021/acs.inorgchem.4c01792es
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses


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Atribución 4.0 InternacionalExcept where otherwise noted, this item's license is described as Atribución 4.0 Internacional