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Sisal-derived acid-char molybdenum catalyst for reductive deoxygenation of sulfoxides

dc.contributor.authorDuarte, Tiago A. G.
dc.contributor.authorMestre, Ana S.
dc.contributor.authorFerreira, Maria J. G.
dc.contributor.authorRego, Ana M. Botelho do
dc.contributor.authorFerraria, Ana M.
dc.contributor.authorKirillova, Marina V.
dc.contributor.authorCarvalho, Ana P.
dc.contributor.authorCalhorda, Maria José
dc.contributor.authorFernandes, Tiago
dc.date.accessioned2025-01-28T19:44:24Z
dc.date.available2025-01-28T19:44:24Z
dc.date.issued2023-09-30
dc.description.abstractThe deoxygenation of sulfoxides is a rather important reaction from both synthetic and biological points of view, due to the potential of sulfides as intermediates in a variety of processes. Homogenous Mo-based catalysts successfully perform the reduction of diphenyl sulfoxide to diphenyl sulfide with high yields but present the well-known limitations regarding recovery and recycling. Thus, in the present work, two new supported catalysts were prepared through the immobilization of molybdenum precursor species (dichlorodioxodi(aquo)molybdenum(VI) and sodium molybdate), onto a sisal-derived acid-char (S13.5), obtained from rope industry wastes by acid-mediated carbonization. The heterogeneous Mo-based materials were characterized by IR spectroscopy, elemental analysis, ICP, solid state NMR, XPS, and SEM, and were evaluated as catalysts for the reduction of sulfoxides to sulfides in the presence of phenylsilane as reducing agent under different reaction conditions. The influence of various experimental parameters, including reducing agent type and amount, solvent type, and acid promoter were investigated. Catalytic studies revealed that both catalysts deoxygenate sulfoxides at 120 °C in toluene solution with high yields (up to 97%). The MoO2Cl2 derived catalyst shown to be highly efficient in the reduction of diaryl, alkylaryl, dibenzyl, and dialkyl sulfoxides to the corresponding sulfoxides using phenylsilane as reductant and no need of acid promoter.eng
dc.description.sponsorshipThis work was supported by Fundaçao ˜ para a Ciˆencia e a Tecnologia (FCT) through projects PEst-OE/FIS/UI0261/2014, PEst-OE/MULTI/ UI0612/2013, UIDB/04046/2020 and UIDP/04046/2020 (BioISI), UIDB/00100/2020 and UIDP/00100/2020 (CQE), Lisboa-01–2020, LA/P/0056/2020 (IMS), UIDB/04565/2020, UIDP/04565/2020 (iBB), LA/P/0140/2020 (i4HB) and 0145FEDER-022125-IST/RNEM. TAF thanks CQB and FCT for a fellowship (PEst-OE/MULTI/00612/2013) and CEECIND/02725/2018 contract. ASM thanks FCT for the CEECIND/01371/2017 contract (Embrace Project). AMF thanks FCT and IST, Portugal, for contract no. IST-ID/131/2018. The authors thank Isabel Dias Nogueira for acquisition and refinement of SEM images. We thank Eng. Mário Dias (LAIST) for ICP-OES experimental assistance.
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.cattod.2023.114388pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.2/19431
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.titleSisal-derived acid-char molybdenum catalyst for reductive deoxygenation of sulfoxideseng
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage114388pt_PT
oaire.citation.startPage114388pt_PT
oaire.citation.titleCatalysis Todaypt_PT
oaire.citation.volume426pt_PT
person.familyNameFernandes
person.givenNameTiago
person.identifier.ciencia-id8810-5C8A-08D0
person.identifier.orcid0000-0002-3374-612X
person.identifier.ridB-6777-2013
person.identifier.scopus-author-id24449123500
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationfc21c4fc-108e-4b02-8413-5b06a96d97cc
relation.isAuthorOfPublication.latestForDiscoveryfc21c4fc-108e-4b02-8413-5b06a96d97cc

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