Photooxidation of alcohols by a porphyrin/quinone/TEMPO system

Takayuki Nagasawa, Suleyman I. Allakhverdiev, Yoshifumi Kimura, Toshi Nagata

    Research output: Contribution to journalArticlepeer-review

    29 Citations (Scopus)


    Photooxidation of alcohols to the corresponding aldehydes with a porphyrin/quinone/TEMPO (TEMPO = 2,2,6,6-tetramethyl-1-piperidinyloxy free radical) system is described. This photoreaction is a combination of a photoinduced electron transfer from the porphyrin to the quinone and a TEMPO-catalyzed oxidation of alcohols triggered by one electron oxidation. The rates of oxidation were in the order of benzylic ≈ allylic > primary ≫ secondary, which is consistent with the intermediacy of the oxoammonium cation derived from TEMPO. Examination of the initial rates suggested that the reaction proceeded via the triplet excited state of the zinc porphyrin. The dependence of initial rates on the oxidation potentials of the porphyrin showed a characteristic bell shape, which is caused by two competitive factors, the efficiency of photoinduced electron transfer and the equilibrium of electron exchange between the porphyrin cation radical and TEMPO. The potential significance of this reaction in photosynthetic model chemistry is briefly discussed.

    Original languageEnglish
    Pages (from-to)174-180
    Number of pages7
    JournalPhotochemical and Photobiological Sciences
    Issue number2
    Publication statusPublished - 2009

    ASJC Scopus subject areas

    • Physical and Theoretical Chemistry


    Dive into the research topics of 'Photooxidation of alcohols by a porphyrin/quinone/TEMPO system'. Together they form a unique fingerprint.

    Cite this