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Isomeric separation in donor–acceptor systems of Pd(II) and Pt(II) and a combined structural, electrochemical and spectroelectrochemical study

  1. 1.
    SYSNO ASEP0369089
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleIsomeric separation in donor–acceptor systems of Pd(II) and Pt(II) and a combined structural, electrochemical and spectroelectrochemical study
    Author(s) Deibel, N. (DE)
    Schweinfurth, D. (DE)
    Fiedler, Jan (UFCH-W) RID, ORCID
    Záliš, Stanislav (UFCH-W) RID, ORCID
    Sarkar, B. (DE)
    Source TitleDalton Transactions. - : Royal Society of Chemistry - ISSN 1477-9226
    Roč. 40, č. 38 (2011), s. 9925-9934
    Number of pages10 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordselectrochemistry ; spectroelectrochemistry ; palladium
    Subject RIVCG - Electrochemistry
    R&D ProjectsLD11086 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000295038400034
    DOI10.1039/C1DT10856E
    AnnotationCompounds of the form [(pap)M(Q2−)] (pap = phenylazopyridine; Q = 3,5-di-tert-butyl-benzoquinone, M = Pd, 1a and 1b, M = Pt, 2a and 2b; Q = 4-tert-butyl-benzoquinone, M = Pd, 3a and 3b; M = Pt, 4a and 4b) were synthesized in a one-pot reaction. The geometrical isomers, which are possible because of the built in asymmetry of these ligands, have been separated by using different temperatures and variable solubility. Structural characterization of 1b shows that the metal centers are in a square planar environment, the pap ligand is in the unreduced neutral state and the quinones are in the doubly reduced, Q2− catecholate form.Cyclic voltammetric measurements on the complexes display two one-electron oxidations and two one-electron reductions. EPR and vis-NIR spectra of the one-electron oxidized forms of the complexes indicate that the first oxidation takes place on the Q2− ligands to produce a metal bound semiquinone (Q−) radical.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2012
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