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dc.contributor.authorSchmitt, Wolfgang
dc.date.accessioned2022-04-04T05:32:24Z
dc.date.available2022-04-04T05:32:24Z
dc.date.created2019en
dc.date.issued2019
dc.date.submitted2019en
dc.identifier.citationChevallot-Beroux E, Ako A.M, Schmitt W, Twamley B, Moran J, Corinne B, Ruhlmann L, Mameri S, Synthesis of new Mn19 analogues and their structural, electrochemical and catalytic properties, Dalton Transactions, 2019, 48, 15, 4830 - 4836en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractWe report the synthesis and structural characterisation of new Mn19 and Mn18M analogues, [MnIII12MnII7(μ4-O)8(μ3-OCH3)2(μ3-Br)6(HLMe)12(MeOH)6]Br2 (2) and [MnIII12MnII6Sr(μ4-O8(μ3-Cl)8(HLMe)12(MeCN)6]Cl2 cluster (3), where H3LMe is 2,6-bis(hydroxymethyl)-p-cresol. The electrochemistry of 2 and 3 has been investigated and their activity as catalysts in the oxidation of benzyl alcohol has been evaluated. Selective oxidation of benzyl alcohol to benzaldehyde by O2 was achieved using 1 mol% of catalyst with conversions of 74% (2) and 60% (3) at 140 °C using TEMPO as a co-catalyst. No partial conversion of benzaldehyde to benzoic acid was observed. The results obtained revealed that different operative parameters – such as catalyst loading, temperature, time, solvent and the presence of molecular oxygen – played an important role in the selective oxidation of benzyl alcohol.en
dc.format.extent4830en
dc.format.extent4836en
dc.language.isoenen
dc.relation.ispartofseriesDalton Transactions;
dc.relation.ispartofseries48;
dc.relation.ispartofseries15;
dc.rightsYen
dc.titleSynthesis of new Mn19 analogues and their structural, electrochemical and catalytic propertiesen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/schmittw
dc.identifier.rssinternalid203993
dc.identifier.doihttp://dx.doi.org/10.1039/c8dt04807j
dc.rights.ecaccessrightsopenAccess
dc.identifier.rssurihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85064172578&doi=10.1039%2fc8dt04807j&partnerID=40&md5=4faa9f089ddfab6447af0d1f3b5b351e
dc.identifier.urihttp://hdl.handle.net/2262/98402


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