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dc.contributor.authorMaitland, Brant
dc.contributor.authorStasch, Andreas
dc.contributor.authorJones, Cameron
dc.date.accessioned2022-06-06T14:30:12Z
dc.date.available2022-06-06T14:30:12Z
dc.date.issued2022-02-18
dc.identifier277083414
dc.identifierafd6bf91-599c-4fa5-ad2c-6b6a2a29c76e
dc.identifier85125890317
dc.identifier.citationMaitland , B , Stasch , A & Jones , C 2022 , ' Extremely bulky β-diketiminate complexes of calcium(II) and ytterbium(II) ' , Australian Journal of Chemistry , vol. Online Early , CH21283 . https://doi.org/10.1071/CH21283en
dc.identifier.issn0004-9425
dc.identifier.otherORCID: /0000-0002-7407-8287/work/109766744
dc.identifier.urihttps://hdl.handle.net/10023/25491
dc.descriptionThis research was supported by the Australian Research Council.en
dc.description.abstractThe potassium salt of an extremely bulky β-diketiminate, [K(Ar*Nacnac)] (Ar*Nacnac = [(Ar*NCMe)2CH]-; Ar* = C6H2Me{C(H)Ph2}2-4,2,6) was reacted with either CaI2 or YbI2(THF)2, which afforded [(Ar*Nacnac)MI] (M = Ca or Yb). These are the first examples of structurally characterised, donor solvent free, N-arene substituted β-diketiminato calcium/ytterbium complexes that incorporate a terminal iodide ligand. Reduction of [(Ar*Nacnac)CaI] with sodium metal gave a complex product mixture, from which a few crystals of the β-diketiminate C-H activated product, [{Ca(μ-Ar*Nacnac-H)}2], were obtained and crystallographically characterised. In an attempt to form a terminal ytterbium hydride compound, treatment of [(Ar*Nacnac)YbI] with K[HBEt3] gave a good yield of the contact ion pair compound [(Ar*Nacnac)Yb(HBEt3)].
dc.format.extent1043266
dc.language.isoeng
dc.relation.ispartofAustralian Journal of Chemistryen
dc.subjectβ‐diketiminateen
dc.subjectBulky liganden
dc.subjectCalciumen
dc.subjectC–H activationen
dc.subjectMetal hydridesen
dc.subjectMetal–metal bondingen
dc.subjectReductionen
dc.subjectYtterbiumen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleExtremely bulky β-diketiminate complexes of calcium(II) and ytterbium(II)en
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.1071/CH21283
dc.description.statusPeer revieweden


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