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Charge transfer in porphyrin–calixarene complexes: ultrafast kinetics, cyclic voltammetry, and DFT calculations

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    SYSNO ASEP0358798
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleCharge transfer in porphyrin–calixarene complexes: ultrafast kinetics, cyclic voltammetry, and DFT calculations
    Author(s) Kubát, Pavel (UFCH-W) RID, ORCID, SAI
    Šebera, Jakub (UFCH-W) ORCID, RID
    Záliš, Stanislav (UFCH-W) RID, ORCID
    Langmaier, Jan (UFCH-W) RID, ORCID, SAI
    Fuciman, M. (CZ)
    Polívka, T. (CZ)
    Lang, Kamil (UACH-T) SAI, RID, ORCID
    Source TitlePhysical Chemistry Chemical Physics. - : Royal Society of Chemistry - ISSN 1463-9076
    Roč. 13, č. 15 (2011), s. 6947-6954
    Number of pages8 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsporphyrin-calixarene complexes ; voltammetry ; DFT calculations
    Subject RIVCF - Physical ; Theoretical Chemistry
    Subject RIV - cooperationInstitute of Inorganic Chemistry - Inorganic Chemistry
    R&D ProjectsGAP208/10/1678 GA ČR - Czech Science Foundation (CSF)
    GA203/09/0691 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    AV0Z40320502 - UACH-T (2005-2011)
    UT WOS000288951000021
    DOI10.1039/C0CP01726D
    AnnotationTransient absorption spectroscopy, cyclic voltammetry, and DFT calculations were used to describe charge transfer processes in a series of 5,10,15,20-tetrakis(N-methylpyridinium-n-yl) porphyrins (TMPyPn, n = 4,3,2) and TMPyPn/p-sulfonatocalix[m]arene (clxm, m = 4,6,8) complexes. Excitation of TMPyPn is accompanied by an increasing electron density at the methylpyridinium substituents in the order TMPyP2 < TMPyP3 < TMPyP4. The quenching of the excited singlet states of the complexes increases with the number of ionized phenolic groups of clxm and can be correlated with the partial transfer of the electron density from O− to the peripheral methylpyridinium substituents rather than to the porphyrin ring.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2012
Number of the records: 1  

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