Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/34321
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dc.contributor.authorNunes, Martinique S.pt_PT
dc.contributor.authorGomes, Diana M.pt_PT
dc.contributor.authorGomes, Ana C.pt_PT
dc.contributor.authorNeves, Patríciapt_PT
dc.contributor.authorMendes, Ricardo F.pt_PT
dc.contributor.authorAlmeida Paz, Filipe A.pt_PT
dc.contributor.authorLopes, André D.pt_PT
dc.contributor.authorValente, Anabela A.pt_PT
dc.contributor.authorGonçalves, Isabel S.pt_PT
dc.contributor.authorPillinger, Martynpt_PT
dc.date.accessioned2022-07-27T09:25:25Z-
dc.date.available2022-07-27T09:25:25Z-
dc.date.issued2021-11-
dc.identifier.issn2073-4344pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/34321-
dc.description.abstractThere is a considerable practical interest in discovering new ways to obtain organomolybdenum heterogeneous catalysts for olefin epoxidation that are easier to recover and reuse and display enhanced productivity. In this study, the complex salt (H2pytz)[MoO2Cl2(pytz)] (1) (Hpytz = 5-(2-pyridyl)tetrazole) has been prepared, structurally characterized, and employed as a precursor for the hydrolysis-based synthesis of a microcrystalline molybdenum oxide/organic hybrid material formulated as [MoO3(Hpytz)] (2). In addition to single-crystal X-ray diffraction (for 1), compounds 1 and 2 were characterized by FT-IR and Raman spectroscopies, solid-state 13C{1H} cross-polarization (CP) magic-angle spinning (MAS) NMR, and scanning electron microscopy (SEM). Compounds 1 and 2 were evaluated as olefin epoxidation catalysts using the model reaction of cis-cyclooctene (Cy8) with tert-butyl hydroperoxide (TBHP), at 70 ºC, which gave 100% epoxide selectivity up to 100% conversion. While 1 behaved as a homogeneous catalyst, hybrid 2 behaved as a heterogeneous catalyst and could be recovered for recycling without showing structural degradation or loss of catalytic performance over consecutive reaction cycles. The substrate scope was broadened to monoterpene DL-limonene (Lim) and biobased unsaturated fatty acid methyl esters, methyl oleate (MeOle), and methyl linoleate (MeLin), which gave predominantly epoxide products.pt_PT
dc.language.isoengpt_PT
dc.publisherMDPIpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50011%2F2020/PTpt_PT
dc.relationPOCI-01-0145-FEDER-030075pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50011%2F2020/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectMolybdenumpt_PT
dc.subjectMolybdenum oxidept_PT
dc.subjectOrganic-inorganic hybrid materialpt_PT
dc.subjectTetrazolept_PT
dc.subject5-(2-pyridyl)tetrazolept_PT
dc.subjectHydrogen bondspt_PT
dc.subjectEpoxidationpt_PT
dc.subjectBio-olefinspt_PT
dc.titleA 5-(2-Pyridyl)tetrazolate Complex of Molybdenum(VI), Its Structure, and Transformation to a Molybdenum Oxide-Based Hybrid Heterogeneous Catalyst for the Epoxidation of Olefinspt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.issue11pt_PT
degois.publication.titleCatalystspt_PT
degois.publication.volume11pt_PT
dc.identifier.doi10.3390/catal11111407pt_PT
dc.identifier.articlenumber1407pt_PT
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