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Indyllithium and the Indyl Anion [InL]- : Heavy Analogues of N-Heterocyclic Carbenes.
Schwamm, Ryan J; Anker, Mathew D; Lein, Matthias; Coles, Martyn P; Fitchett, Christopher M.
Affiliation
  • Schwamm RJ; School of Chemical and Physical Sciences, Victoria University of Wellington, PO Box 600, Wellington, 6012, New Zealand.
  • Anker MD; School of Chemical and Physical Sciences, Victoria University of Wellington, PO Box 600, Wellington, 6012, New Zealand.
  • Lein M; School of Chemical and Physical Sciences, Victoria University of Wellington, PO Box 600, Wellington, 6012, New Zealand.
  • Coles MP; School of Chemical and Physical Sciences, Victoria University of Wellington, PO Box 600, Wellington, 6012, New Zealand.
  • Fitchett CM; Department of Chemistry, University of Canterbury, Private Bag 4800, Christchurch, 8041, New Zealand.
Angew Chem Int Ed Engl ; 57(20): 5885-5887, 2018 05 14.
Article in En | MEDLINE | ID: mdl-29575533
Reduction of the indate complex In(NONAr )(µ-Cl)2 Li(OEt2 )2 (NONAr =[O(SiMe2 NAr)2 ]2- ; Ar=2,6-iPr2 C6 H3 ) with sodium generates the InII diindane species [In(NONAr )]2 . Further reduction with a mixture of potassium and [2.2.2]crypt affords the InI N-heterocyclic indyl anion [In(NONAr )]- , which crystallizes with a non-contacted [K([2.2.2]crypt)]+ cation. The indyl anion can also be isolated as the indyllithium compound In(NONAr )(Li{THF}3 ), which contains an In-Li bond. Density functional theory calculations show that the HOMO of the indyl anion is a metal-centred lone pair, and preliminary reactivity studies confirm its nucleophilic behaviour.
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Full text: 1 Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2018 Type: Article Affiliation country: New Zealand

Full text: 1 Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2018 Type: Article Affiliation country: New Zealand