Sweet switches: azobenzene glycoconjugates synthesized by click chemistry

Chem Commun (Camb). 2012 Aug 4;48(60):7519-21. doi: 10.1039/c2cc33542e. Epub 2012 Jun 25.

Abstract

Azobenzene glycoconjugates can be switched between two isomeric states, E and Z, to change the spatial orientation of the conjugated carbohydrate ligands. Mono-, di- and trivalent azobenzene glycoconjugates were synthesized using click chemistry and their photochromic properties determined. Multivalency effects were observed in photoisomerisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemical synthesis*
  • Azo Compounds / chemistry
  • Click Chemistry / methods*
  • Glycoconjugates / chemical synthesis*
  • Glycoconjugates / chemistry
  • Isomerism
  • Photochemical Processes

Substances

  • Azo Compounds
  • Glycoconjugates
  • azobenzene