Megalo-Cavitands: Synthesis of Acridane[4]arenes and Formation of Large, Deep Cavitands for Selective C70 Uptake

Angew Chem Int Ed Engl. 2022 Oct 17;61(42):e202209885. doi: 10.1002/anie.202209885. Epub 2022 Sep 8.

Abstract

Deep cavitands, concave molecular containers, represent an important supramolecular host class that has been explored for a variety of applications ranging from sensing, switching, purification and adsorption to catalysis. A major limitation in the field has been the cavitand volume that is restricted by the size of the structural platform utilized (diameter approx. 7 Å). We here report the synthesis of a novel, unprecedentedly large structural platform, named acridane[4]arene (diameter approx. 14 Å), suitable for the construction of cavitands with volumes of up to 814 Å3 . These megalo-cavitands serve as size-selective hosts for fullerenes with mM to sub-μM binding affinity for C60 and C70 . Furthermore, the selective binding of fullerene C70 in the presence of C60 was demonstrated.

Keywords: Calixarene; Deep Cavitands; Host-Guest Systems; Macrocycles; Supramolecular Chemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ethers, Cyclic
  • Fullerenes* / chemistry
  • Resorcinols

Substances

  • Ethers, Cyclic
  • Fullerenes
  • Resorcinols
  • cavitand