4.8 Article

Proton-Coupled Oxygen Reduction at Liquid-Liquid Interfaces Catalyzed by Cobalt Porphine

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 37, Pages 13453-13459

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja904569p

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Funding

  1. EPFL
  2. Swiss National Science Foundation [FNRS 200020-116588]
  3. CNRS
  4. Grant Agency of the Czech Republic [203/07/1257]
  5. European Cost Action [D36/007/06]
  6. Scientific and Technological Research Council of Turkey (TUBITAK)

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Cobalt porphine (COP) dissolved in the organic phase of a biphasic system is used to catalyze O-2 reduction by an electron donor, ferrocene (Fc). Using voltammetry at the interface between two immiscible electrolyte solutions (ITIES), it is possible to drive this catalytic reduction at the interface as a function of the applied potential difference, where aqueous protons and organic electron donors combine to reduce O-2. The current signal observed corresponds to a proton-coupled electron transfer (PCET) reaction, as no current and no reaction can be observed in the absence of either the aqueous acid, COP, c, or O-2.

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