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dc.contributor.authorBAKER, ROBERTen
dc.date.accessioned2014-06-03T13:24:28Z
dc.date.available2014-06-03T13:24:28Z
dc.date.issued2002en
dc.date.submitted2002en
dc.identifier.citationR.J. Baker, M.L. Cole, C. Jones and M.F. Mahon,, Bidentate N-Heterocyclic carbene complexes of group 13 trihydrides and trihalides., J. Chem. Soc., Dalton Trans, 2002, 1992, 1996en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/69579
dc.descriptionPUBLISHEDen
dc.description.abstracttop Treatment of the potentially chelating bis-carbene, 1,2-ethylene-3,3′-di-tert-butyl-diimidazole-2,2′-diylidene, EtIBut, with [MH3(NMe3)], M = Al, Ga, In, in a 1 ∶ 1 or 1 ∶ 2 stoichiometery led to good yields of the metal rich 2 ∶ 1 adducts, [(MH3)2(μ-EtIBut)]. These complexes have been spectroscopically characterised and the X-ray crystal structures of two (M = Al or In) obtained. In contrast, the 1 ∶ 1 or 1 ∶ 2 reactions of EtIBut with MX3, M = In or Tl, X = Br or Cl, led to the 1 ∶ 1 adducts, [MX3(EtIBut)]. The X-ray crystal structure of one of these, [InBr3(EtIBut)], shows the ligand to act in a chelating mode, taking up equatorial positions of an trigonal bipyramid. The reactions of EtIBut with MCl3, M = Al or Ga, led to decomposition and in the aluminium reaction the major product of the decomposition process was the bis-imidazolium salt, [EtIButH2][Cl]2, which has also been crystallographically characterised. Several related reactions are described.en
dc.format.extent1992en
dc.format.extent1996en
dc.language.isoenen
dc.relation.ispartofseriesJ. Chem. Soc., Dalton Transen
dc.rightsYen
dc.subjectChemistryen
dc.titleBidentate N-Heterocyclic carbene complexes of group 13 trihydrides and trihalides.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/bakerrjen
dc.identifier.rssinternalid57399en
dc.identifier.doihttp://dx.doi.org/10.1039/b200500jen
dc.rights.ecaccessrightsopenAccess


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