Aziridinofullerene: a versatile platform for functionalized fullerenes

J Am Chem Soc. 2011 Mar 2;133(8):2402-5. doi: 10.1021/ja111213k. Epub 2011 Feb 8.

Abstract

An aziridine moiety on the fullerene core can serve as an acid-triggered reacting template for the controlled synthesis of a range of functionalized fullerenes that are otherwise difficult to synthesize in an efficient and selective manner. A copper-catalyzed aziridination of C(60) for the practical synthesis of aziridinofullerene 1 and acid-catalyzed reactions of 1 with mono- and bifunctional nucleophiles as well as alkynes are described. The rapid generation of structural diversity in a single chemical operation using the common platform 1 is notable.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aziridines / chemistry*
  • Fullerenes / chemistry*
  • Ligands
  • Molecular Structure

Substances

  • Aziridines
  • Fullerenes
  • Ligands
  • fullerene C60