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Electrochemical evidence of catalysis of oxygen reduction at the polarized liquid–liquid interface by tetraphenylporphyrin monoacid and diacid

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    SYSNO ASEP0330442
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleElectrochemical evidence of catalysis of oxygen reduction at the polarized liquid–liquid interface by tetraphenylporphyrin monoacid and diacid
    TitleElektrochemický důkaz katalytické redukce kyslíku protonizovaným a diprotonizovaným tetraphenylporphyrinem na polarizovaném rozhraní nemísitelných roztoků elektrolytů
    Author(s) Trojánek, Antonín (UFCH-W) RID
    Langmaier, Jan (UFCH-W) RID, ORCID, SAI
    Su, B. (CH)
    Girault, H. H. (CH)
    Samec, Zdeněk (UFCH-W) RID, ORCID
    Source TitleElectrochemistry Communications. - : Elsevier - ISSN 1388-2481
    Roč. 11, č. 10 (2009), s. 1940-1943
    Number of pages4 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsliquid-liquid interface ; oxygen reduction ; decamethylferrocene ; catalysis
    Subject RIVCG - Electrochemistry
    R&D ProjectsGA203/07/1257 GA ČR - Czech Science Foundation (CSF)
    OC 177 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000271571300024
    DOI10.1016/j.elecom.2009.08.022
    AnnotationCyclic voltammetry is used to study the role of 5,10,15,20-tetraphenyl-21H,23H-porphine (H2TPP) in the reduction of molecular oxygen by decamethylferrocene (DMFc) at the polarized water|1,2-dichloroethane (DCE) interface. It is shown that this rather slow reaction proceeds remarkably faster in the presence of tetraphenylporphyrin monoacid (H3TPP+) and diacid (H4TPP2+), which are formed in DCE by the successive transfer of two protons from the acidified aqueous phase. A mechanism is proposed, which includes the formation of adduct between H3TPP+ or H4TPP2+ and O2 that is followed by electron transfer from DMFc to the adduct leading to the observed production of DMFc+ and to the regeneration of H2TPP or H3TPP+, respectively.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2010
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