Beilstein Journal of Organic Chemistry (Jun 2014)

Multichromophoric sugar for fluorescence photoswitching

  • Stéphane Maisonneuve,
  • Rémi Métivier,
  • Pei Yu,
  • Keitaro Nakatani,
  • Juan Xie

DOI
https://doi.org/10.3762/bjoc.10.151
Journal volume & issue
Vol. 10, no. 1
pp. 1471 – 1481

Abstract

Read online

A multichromophoric glucopyranoside 2 bearing three dicyanomethylenepyran (DCM) fluorophores and one diarylethene (DAE) photochrome has been prepared by Cu(I)-catalyzed alkyne–azide cycloaddition reaction. The fluorescence of 2 was switched off upon UV irradiation, in proportion with the open to closed form (OF to CF) conversion extent of the DAE moiety. A nearly 100% Förster-type resonance energy transfer (FRET) from all three DCM moieties to a single DAE (in its CF) moiety was achieved. Upon visible irradiation, the initial fluorescence intensity was recovered. The observed photoswiching is reversible, with excellent photo resistance.

Keywords