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Spontaneous mirror-symmetry breaking coupled to top-bottom chirality transfer: from porphyrin self-assembly to scalemic Diels-Alder adducts.

Aitor ArleguiBernat SolerAlex GalindoOriol ArteagaAdolf CanillasJosep M RibóZoubir El-HachemiJoaquim CrusatsAlbert Moyano
Published in: Chemical communications (Cambridge, England) (2019)
This report shows how the net supramolecular chirality that emerged by spontaneous mirror-symmetry breaking (SMSB) at the mesoscale level can be transferred towards asymmetric solution chemistry. The J-aggregates obtained by self-assembly of an achiral porphyrin act as chiral counteranions in an iminium-promoted Diels-Alder reaction, leading to enantiomeric imbalances in the final adducts.
Keyphrases
  • electron transfer
  • photodynamic therapy
  • energy transfer
  • capillary electrophoresis
  • metal organic framework
  • solid state
  • ionic liquid
  • drug discovery
  • water soluble