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Chiral Cationic [Cp′Mo(CO)2(NCMe)]+ Species – Catalyst Precursors for Olefin Epoxidation with H2O2 and tert-Butyl Hydroperoxide

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dc.contributor.authorReis, Patrícia
dc.contributor.authorGamelas ou Carla A. Gamelas, Carla
dc.contributor.authorBrito, José
dc.contributor.authorSaffon, Nathalie
dc.contributor.authorGoméz, Montserrat
dc.contributor.authorRoyo, Beatriz
dc.date.accessioned2018-03-13T14:54:15Z
dc.date.available2018-03-13T14:54:15Z
dc.date.issued2011
dc.description.abstractA novel cyclopentadienyl ligand bearing a chiral oxazoline pendant group (Cpox) has been prepared. Its coordination to molybdenum and tungsten afforded optically pure (R)-CpoxM(η3-C3H5)(CO)2 (M = Mo, W) in which the pendant oxazoline fragment is not coordinated to the metal center. Reaction of (R)-CpoxMo(η3-C3H5)(CO)2 with tetrafluoroboric acid gives the bidentate η5-cyclopentadienyloxazoline complex [CpoxMo(CO)2(NCMe)]BF4 in which the oxazoline is coordinated through the N-atom to the molybdenum center. Their catalytic performance in the epoxidation of cis-cyclooctene, (R)-limonene, and trans-β-methylstyrene with H2O2 and tert-butyl hydroperoxide (TBHP) as oxidants has been studied. (R)-CpoxW(η3-C3H5)(CO)2 displayed high catalytic activity achieving quantitative conversion of cyclooctene epoxide in 2 h with H2O2. [CpoxMo(CO)2(NCMe)]+ has been shown to be an efficient catalyst with TBHP and H2O2, reaching quantitative conversions of the corresponding epoxide in 30 min and 11 h, respectively. ESI-MS studies of the reaction of [CpoxMo(CO)2(NCMe)]+ with H2O2 and TBHP revealed the in situ formation of the corresponding peroxido [CpoxMo(O2)O]+ and dioxido [CpoxMoO2]+ species, respectively. Further oxidation of these complexes resulted in the loss of the cyclopentadienyloxazoline ligand. Based on spin trap experiments, the involvement of both carbon- and oxygen-centred radicals in the olefin epoxidation catalyzed by [CpoxMo(CO)2(NCMe)]+ has been proved.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationReis, P., Gamelas, C., Brito, J., Saffon, N., Gómez, M. & Royo, B. (2011). Chiral Cationic [Cp′Mo(CO)2(NCMe)]+ Species: Catalyst Precursors for Olefin Epoxidation with H2O2 and tert-Butyl Hydroperoxide. European Journal of Inorganic Chemistry, 2011(5), pp. 666-673. doi: 10.1002/ejic.201001065pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.26/21979
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.titleChiral Cationic [Cp′Mo(CO)2(NCMe)]+ Species – Catalyst Precursors for Olefin Epoxidation with H2O2 and tert-Butyl Hydroperoxidept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage673pt_PT
oaire.citation.startPage666pt_PT
oaire.citation.titleEuropean Journal of Inorganic Chemistrypt_PT
person.familyNameGamelas Albuquerque Pinto Reis
person.givenNameCarla Alexandra
person.identifier.ciencia-id2219-54F2-BB9D
rcaap.rightsclosedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationa02aa459-55c4-4506-b8f2-5189e5c13124
relation.isAuthorOfPublication.latestForDiscoverya02aa459-55c4-4506-b8f2-5189e5c13124

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