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Isoflurane as a solvent for electrochemistry. Electrooxidation study of icosahedral carborane anions in four different solvents

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    SYSNO ASEP0386134
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleIsoflurane as a solvent for electrochemistry. Electrooxidation study of icosahedral carborane anions in four different solvents
    Author(s) Wahab, Abdul (UFCH-W)
    Kvapilová, Hana (UFCH-W) RID
    Klíma, Jiří (UFCH-W) RID
    Michl, Josef (UOCHB-X) RID, ORCID
    Ludvík, Jiří (UFCH-W) RID, ORCID
    Source TitleJournal of Electroanalytical Chemistry. - : Elsevier - ISSN 1572-6657
    Roč. 689, JAN 2013 (2013), s. 257-261
    Number of pages5 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsisoflurane ; relative permitivity ; icosahedral carborane anions
    Subject RIVCG - Electrochemistry
    R&D ProjectsME09002 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GC203/09/J058 GA ČR - Czech Science Foundation (CSF)
    Institutional supportUFCH-W - RVO:61388955 ; UOCHB-X - RVO:61388963
    UT WOS000317161300036
    EID SCOPUS84871789455
    DOI10.1016/j.jelechem.2012.10.002
    AnnotationVoltammetric studies of icosahedral carborane anions View the MathML source (1), View the MathML source (2), View the MathML source (3), and View the MathML source (4) are reported in isoflurane (1-chloro-2,2,2-trifluoroethyl difluoromethyl ether) and in three other solvents with different polarity (liquid SO2, acetonitrile, dichloromethane). They demonstrate the first use of isoflurane as a non-polar electrochemical solvent. The anions 1, 2 and 3 show reversible one-electron oxidations in all four solvents, whereas the oxidation of 4 is irreversible even at high scan rates. The measured half-wave potentials (E1/2) show a remarkable variation in the four different solvents. The E1/2 values are discussed in terms of specific solvation of the anions. The experimental results correlate fairly well with density functional theory (DFT) calculations.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2014
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