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dc.date.accessioned2023-11-09T16:36:44Z
dc.date.available2023-11-09T16:36:44Z
dc.date.created2023-10-12T11:43:37Z
dc.date.issued2023
dc.identifier.citationVesseur, David Holmsen, Marte Sofie Martinsen Bourissou, Didier . Au(III) π-Allyl Complexes: Synthesis, Structure, Reactivity, and Catalytic Applications. ChemCatChem. 2023
dc.identifier.urihttp://hdl.handle.net/10852/105764
dc.description.abstractAbstract π‐Allyl complexes of transition metals are key species in organometallic chemistry and homogeneous catalysis. Palladium(II) π‐allyl complexes in particular, have gained a lot of attention, but their isoelectronic gold(III) counterparts long remained elusive. However, this situation changed during the last few years. This concept article describes the preparative routes, characterization, structure and reactivity of such species, together with their catalytic applications. The influence of the ancillary ligand at gold, either (P,C)/(N,C)‐cyclometalated or (P,N)‐hemilabile, is analysed in detail. The Au(III) and Pd(II) π‐allyl complexes are also compared to highlight the similarities and differences.
dc.languageEN
dc.publisherWiley - VCH Verlag GmbH
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAu(III) π-Allyl Complexes: Synthesis, Structure, Reactivity, and Catalytic Applications
dc.title.alternativeENEngelskEnglishAu(III) π-Allyl Complexes: Synthesis, Structure, Reactivity, and Catalytic Applications
dc.typeJournal article
dc.creator.authorVesseur, David
dc.creator.authorHolmsen, Marte Sofie Martinsen
dc.creator.authorBourissou, Didier
cristin.unitcode185,15,17,1
cristin.unitnameAnsatte SMN
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2184079
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=ChemCatChem&rft.volume=&rft.spage=&rft.date=2023
dc.identifier.jtitleChemCatChem
dc.identifier.volume15
dc.identifier.issue20
dc.identifier.doihttps://doi.org/10.1002/cctc.202300851
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1867-3880
dc.type.versionPublishedVersion
cristin.articleide202300851
dc.relation.projectNFR/315004


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