Ceo as a photocatalyst of electron-transfer processes: reactions of triplet ceo with chloranil, perylene, and tritolylamine studied by flash photolysis and FT-EPR

Carlos A. Steren, Hans Van Willigen, Laszlo Biczök, Neeraj Gupta, Henry Linschitz

Research output: Contribution to journalArticle

101 Citations (Scopus)

Abstract

Photoprocesses in benzonitrile solutions of Ceo and chloranil (CA) have been studied by complementary techniques of nanosecond laser photolysis and Fourier transform EPR. Direct oxidation of 3C6o by CA is slow (k -(2.0 ±0.3) x 107 M"1 s~'). consistent with the high oxidation potential of 3Ceo- However, the formation rate and yield of CA~ are much increased by addition of perylene (Pe) or tritolylamine (TTA) via the fast reactions 3C60 + Pe -CM + 3Pe, followed by 3Pe + CA -Pe+ + CA~, or 3C6o + TTA -Ceo~ + TTA+, followed by C60- + CA -Ceo + CA~. These reactions utilize the broad absorption and initial high triplet yield of Ceo, as well as the low oxidation potential of 3Pe or high reduction potential of 3Ceo, to catalyze efficient formation of CA~ and enhance separation of radicals. Triplet Ceo also reacts with Pe by electron transfer, forming Pe+ and Ceo~ with rate one-third that of energy transfer. However, the CA~ formed in the Pe-catalyzed reaction is strongly spin-polarized, indicating that it is formed primarily via the 3Pe pathway. The extinction coefficient of C60- at 1080 nm is measured (e -18 300 ±1100 M~' cm"1) using the TTA reaction.

Original languageEnglish
Pages (from-to)8920-8926
Number of pages7
JournalJournal of physical chemistry
Volume100
Issue number21
DOIs
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Engineering(all)
  • Physical and Theoretical Chemistry

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