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Synergic Deprotonation Generates Alkali-Metal Salts of Tethered Fluorenide-NHC Ligands Co-Complexed to Alkali-Metal Amides.

Kieren J EvansStephen M Mansell
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
Synergic combinations of alkali-metal hydrocarbyl/amide reagents were used to synthesise saturated N-heterocyclic carbene (NHC) ligands tethered to a fluorenide anion through deprotonation of a spirocyclic precursor, whereas conventional bases were not successful. The Li2 derivatives displayed a bridging amide between two Li atoms within the fluorenide-NHC pocket, whereas the Na2 and K2 analogues displayed extended solid-state structures with the fluorenide-NHC ligand chelating one alkali metal centre.
Keyphrases
  • solid state
  • ionic liquid
  • high resolution
  • molecular docking
  • ion batteries