Catalytic Advantages of SO3H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel–Crafts Acylation Reaction
dc.contributor.author | Bauza, Marta | |
dc.contributor.author | Leo, Pedro | |
dc.contributor.author | Palomino Cabello, Carlos | |
dc.contributor.author | Martín, Antonio | |
dc.contributor.author | Orcajo, Gisela | |
dc.contributor.author | Turnes Palomino, Gemma | |
dc.contributor.author | Martínez, Fernando | |
dc.date.accessioned | 2024-09-11T07:37:49Z | |
dc.date.available | 2024-09-11T07:37:49Z | |
dc.date.issued | 2024-09-03 | |
dc.description.abstract | The 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 integrity | es |
dc.identifier.citation | Bauza, 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.4c01792 | es |
dc.identifier.doi | 10.1021/acs.inorgchem.4c01792 | es |
dc.identifier.issn | 0020-1669 (print) | |
dc.identifier.issn | 1520-510X (online) | |
dc.identifier.uri | https://hdl.handle.net/10115/39468 | |
dc.language.iso | eng | es |
dc.publisher | American Chemical Society | es |
dc.rights | Atribución 4.0 Internacional | * |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | Catalysts | es |
dc.subject | Chemical synthesis | es |
dc.subject | Materials Organic reactions | es |
dc.subject | Post-translational modification | es |
dc.title | Catalytic Advantages of SO3H-Modified UiO-66(Zr) Materials Obtained via Microwave Synthesis in Friedel–Crafts Acylation Reaction | es |
dc.type | info:eu-repo/semantics/article | es |
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