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dc.contributor.authorMartínez-Vivas, Sebastián
dc.contributor.authorGonell, Sergio
dc.contributor.authorPoyatos, Macarena
dc.contributor.authorPeris, Eduardo
dc.date.accessioned2024-05-31T07:05:16Z
dc.date.available2024-05-31T07:05:16Z
dc.date.issued2024-05-01
dc.identifier.citationSebastián Martínez-Vivas, Sergio Gonell, Macarena Poyatos, and Eduardo Peris. “Anion-Switchable” Pincer-Mn(I) Catalyst for the Reductive N-Methylation of Amines with Formic Acid and CO2. ACS Catalysis 2024 14 (10), 7600-7608 DOI: 10.1021/acscatal.4c01812ca_CA
dc.identifier.issn2155-5435
dc.identifier.urihttp://hdl.handle.net/10234/207562
dc.description.abstractWe report a manganese(I) complex of formula [Mn(NDI-CNC)(CO)3](BArF4), in which NDI-CNC refers to a pincer pyridine-bis-imidazolylidene ligand functionalized with a naphthalene-diimide (NDI) moiety. Due to the presence of the NDI fragment, the electron-donating strength of the pincer ligand can be increased by producing an electrochemical reduction of the NDI moiety or by the addition of tetrabutylammonium chloride (TBACl). The extent of the changes produced in the electron-donating power of the pincer ligand can be quantified by studying the variation of the C–O stretching frequencies by infrared spectroscopy. It is observed that the catalytic activity of the manganese complex in the reductive methylation of a series of secondary amines with formic acid (or CO2) in the presence of PhSiH3 is almost negligible, but the catalyst can be turned very active in the presence of TBACl. This study constitutes a rare example of an anion-sensitive catalyst. Furthermore, the activity of the catalyst can be switched on and off for several cycles by subsequent addition of TBACl or NOBF4, respectively.ca_CA
dc.description.sponsorShipFunding for open access charge: CRUE-Universitat Jaume I
dc.format.extent9 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.relationNHCS inteligentes para la obtención de ensamblajes supramoleculares y catalizadores conmutablesca_CA
dc.relationLigandos inteligentes para la reducción de CO2 (OUTCO2)ca_CA
dc.relation.isPartOfACS Catalysis, 2024, vol. 14, no 14ca_CA
dc.rightsCopyright © 2024 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.ca_CA
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/ca_CA
dc.subjectmanganeseca_CA
dc.subjectCO2 reductionca_CA
dc.subjectmethylation of aminesca_CA
dc.subjectpincer ligandsca_CA
dc.subjectswitchable catalystsca_CA
dc.subjectanion-sensitive ligandsca_CA
dc.title“Anion-Switchable” Pincer-Mn(I) Catalyst for the Reductive N-Methylation of Amines with Formic Acid and CO2ca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttps://doi.org/10.1021/acscatal.4c01812
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.relation.publisherVersion“Anion-Switchable” Pincer-Mn(I) Catalyst for the Reductive N-Methylation of Amines with Formic Acid and CO2ca_CA
dc.description.sponsorshipWe gratefully acknowledge financial support from the Ministerio de Ciencia y Universidades (PID2021-127862NBI00 and TED2021-130647B−I00) and the Universitat Jaume I (UJI-B2020-01 and UJI-B2021-39). We are grateful to the Serveis Centrals d’Instrumentació Científica (SCIC-UJI) for providing spectroscopic facilities.
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_CA
project.funder.identifierhttp://dx.doi.org/10.13039/501100011033ca_CA
project.funder.nameMinisterio de Ciencia e Innovaciónca_CA
project.funder.nameUniversitat Jaume Ica_CA
oaire.awardNumberMCIN/PEICTI2021-2023/PID2021-127862NB-I00ca_CA
oaire.awardNumberMCIN/PEICTI2021-2023/TED2021-130647B-I00ca_CA
oaire.awardNumberUJI-B2020-01ca_CA
oaire.awardNumberUJI-B2021-39ca_CA


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Copyright © 2024 The Authors. Published by American Chemical Society. This publication is licensed under  CC-BY 4.0.
Excepto si se señala otra cosa, la licencia del ítem se describe como: Copyright © 2024 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.