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dc.contributor.authorSongis, Olivier
dc.contributor.authorCazin, Catherine S.J.
dc.date.accessioned2014-09-16T23:01:42Z
dc.date.available2014-09-16T23:01:42Z
dc.date.issued2013-09-17
dc.identifier136182885
dc.identifier3efff3ab-ac02-42ec-8ecc-97da17b1d01f
dc.identifier000325540000002
dc.identifier84883809595
dc.identifier.citationSongis , O & Cazin , C S J 2013 , ' [Pd(NHC)(PR3)] complexes : versatile tools for tandem dehydrogenation-hydrogenation processes ' , Synlett , vol. 24 , no. 15 , pp. 1877-1881 . https://doi.org/10.1055/s-0033-1339669en
dc.identifier.issn0936-5214
dc.identifier.urihttps://hdl.handle.net/10023/5421
dc.descriptionThis work is supported in part by funding from the EPSRC UKen
dc.description.abstractHomogeneous Pd(0) complexes are powerful tools for numerous catalytic reactions. Recent work has demonstrated the unique properties displayed by [Pd(NHC)(PR3)] catalysts in the activation of ammonia borane (AB) and formic acid, with the subsequent formation of hydrogen. An understanding of the mechanism allowed for the design of a new dehydrogenation-hydrogenation tandem process using hydrogen storage materials'. The hydrogenations of alkenes and alkynes were successfully performed at low catalyst loadings of Pd(0) species and mild conditions. Such tandem process represents a safe and innovative alternative to classic hydrogenation protocols.
dc.format.extent5
dc.format.extent695314
dc.language.isoeng
dc.relation.ispartofSynletten
dc.subjectTandem reactionen
dc.subjectHydrogenationen
dc.subjectDehydrogenationen
dc.subjectPd(0)en
dc.subjectHydrogen storage materialen
dc.subjectN-heterocyclic carbeneen
dc.subjectAsymmetric hydrogenationen
dc.subjectCatalystsen
dc.subjectPalladiumen
dc.subjectNHCen
dc.subjectRouteen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.title[Pd(NHC)(PR3)] complexes : versatile tools for tandem dehydrogenation-hydrogenation processesen
dc.typeJournal articleen
dc.contributor.sponsorThe Royal Societyen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1055/s-0033-1339669
dc.description.statusPeer revieweden
dc.date.embargoedUntil2014-09-17
dc.identifier.grantnumberUF100691en


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