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Indyllithium and the Indyl Anion [InL]- : Heavy Analogues of N-Heterocyclic Carbenes.

Ryan J SchwammMathew D AnkerMatthias LeinMartyn P ColesChristopher M Fitchett
Published in: Angewandte Chemie (International ed. in English) (2018)
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.
Keyphrases
  • density functional theory
  • ionic liquid
  • molecular dynamics
  • ion batteries
  • solid state
  • molecular dynamics simulations
  • molecular docking
  • genetic diversity