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Reversible crystal-to-crystal chiral resolution: making/breaking non-bonding SO interactions.

R Alex MayoDavid J SullivanTravis A P FillionStefan W KyciaDmitriy V SoldatovKathryn E Preuss
Published in: Chemical communications (Cambridge, England) (2018)
An achiral organic molecule adopts a chiral conformation, crystallizing in two morphologies: a racemic form, stable <70 °C, and a homochiral form, stable ≥70 °C. Upon seeding, crystal-to-crystal phase transitions occur reversibly between the racemic and chiral forms. Liquid-to-solid chiral crystallization is observed >90% of the time from the melt.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • solid state
  • mass spectrometry
  • molecular dynamics simulations
  • single molecule
  • water soluble