Photonic switching of photoinduced electron transfer in a dithienylethene-porphyrin-fullerene triad molecule

Paul A. Liddell, Gerdenis Kodis, Ana L. Moore, Thomas A. Moore, Devens Gust

Research output: Contribution to journalArticlepeer-review

216 Citations (Scopus)

Abstract

A dithienylethene (DTE)-porphyrin (P)-fullerene (C60) triad molecule in which intramolecular photoinduced electron transfer is controlled by the photochromic DTE moiety has been prepared. Irradiation of the molecule with visible light gives the open form of the dithienylethene (DTEo). Excitation of the porphyrin gives DTEo-1P-C60, which undergoes photoinduced electron transfer with a time constant of 25 ps to generate DTEo-P•+-C60•-. Irradiation with ultraviolet light produces the closed form of the dithienylethene (DTEc). Excitation of DTEc-P-C60 yields DTEc-1P-C60, whose porphyrin first excited singlet state is quenched in 2.3 ps by singlet-singlet energy transfer to DTEc, generating 1DTEc-P-C60 and precluding significant photoinduced electron transfer. Such highly reversible photonically controlled intramolecular photoinduced electron transfer may eventually be useful in the design of photonic or optoelectronic devices.

Original languageEnglish
Pages (from-to)7668-7669
Number of pages2
JournalJournal of the American Chemical Society
Volume124
Issue number26
DOIs
Publication statusPublished - Jul 3 2002

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

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