Aromatic aldehyde oxidation by hexacyanoferrate(III) catalyzed by Ru(VI) in alkaline medium
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Química Física | |
| dc.contributor.author | Alcolado Olivares, Clara Inés | |
| dc.contributor.author | Poblete Pérez, Javier | |
| dc.contributor.author | García Río, Luis | |
| dc.contributor.author | Jiménez Martínez, Elena | |
| dc.contributor.author | Poblete Martín, Francisco Javier | |
| dc.date.accessioned | 2025-12-11T10:36:44Z | |
| dc.date.available | 2025-12-11T10:36:44Z | |
| dc.date.issued | 2024-01-01 | |
| dc.description.abstract | In this study, the selective oxidation of aromatic aldehydes has been investigated using Ru(VI) as a catalyst and hexacyanoferrate (III) as a cooxidant in an alkaline medium. The reaction order with respect to the oxidant and the aromatic aldehyde is complex while the reaction order with respect to Ru(VI) is one. The proposed mechanism presents two catalytic cycles for the two active species of the catalyst. In each cycle, Ru(VI) species forms a complex with the anion of hydrated benzaldehyde which decomposes to form benzoic acid. The function of hexacyanoferrate(III) is the regeneration of catalyst species. A quantitative structure–activity relationship was analyzed using the Hammett equation for decomposition complex step. This analysis showed that deactivating groups in para- position enhances this process | |
| dc.description.peerreviewed | SI | |
| dc.description.sponsorship | inancial support from the University of Castilla-La Mancha and the European Regional Development Fund (FEDER) (grant n° 2023-GRIN-34143) is gratefully acknowledged | |
| dc.identifier.citation | C.I. Alcolado, J. Poblete, L. García-Río, E. Jiménez, F.J. Poblete, Aromatic aldehyde oxidation by hexacyanoferrate(III) catalyzed by Ru(VI) in alkaline medium, Journal of Molecular Liquids, Volume 393, 2024, 123580, ISSN 0167-7322, https://doi.org/10.1016/j.molliq.2023.123580 | |
| dc.identifier.doi | 10.1016/j.molliq.2023.123580 | |
| dc.identifier.issn | 0167-7322 | |
| dc.identifier.uri | https://hdl.handle.net/10347/44400 | |
| dc.journal.title | Journal of Molecular Liquids | |
| dc.language.iso | eng | |
| dc.publisher | Elsevier | |
| dc.relation.publisherversion | https://doi.org/10.1016/j.molliq.2023.123580 | |
| dc.rights | © 2023 The Author(s). Published by Elsevier B.V. This article is available under the Creative Commons CC-BY-NC license | |
| dc.rights | Attribution-NonCommercial 4.0 International | en |
| dc.rights.accessRights | open access | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | |
| dc.subject | Oxidation mechanism | |
| dc.subject | Aromatic aldehydes | |
| dc.subject | Ruthenate ion | |
| dc.subject | Hexacyanoferrate(III) | |
| dc.subject | Alkaline medium | |
| dc.title | Aromatic aldehyde oxidation by hexacyanoferrate(III) catalyzed by Ru(VI) in alkaline medium | |
| dc.type | journal article | |
| dc.type.hasVersion | VoR | |
| dc.volume.number | 393 | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 064dadbb-9bec-42da-b1d5-d961ce90c30f | |
| relation.isAuthorOfPublication.latestForDiscovery | 064dadbb-9bec-42da-b1d5-d961ce90c30f |
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