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Ultrafast Excited-State Dynamics ef [Re(L)(CO)(3)(bpy)](n) Complexes: Involvement of the Solvent

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    SYSNO ASEP0347663
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleUltrafast Excited-State Dynamics ef [Re(L)(CO)(3)(bpy)](n) Complexes: Involvement of the Solvent
    Author(s) Nahhas, A. E. (CH)
    Cannizzo, A. (CH)
    van Mourik, F. (CH)
    Blanco-Rodríguez, A. M. (GB)
    Záliš, Stanislav (UFCH-W) RID, ORCID
    Vlček, Antonín (UFCH-W) RID, ORCID
    Chergui, M. (CH)
    Source TitleJournal of Physical Chemistry A. - : American Chemical Society - ISSN 1089-5639
    Roč. 114, č. 22 (2010), s. 6361-6369
    Number of pages9 s.
    Languageeng - English
    CountryUS - United States
    Keywordsultrafast excited-state dynamics ; spectroscopy ; TD-DFT
    Subject RIVCG - Electrochemistry
    R&D ProjectsOC09043 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000278300600003
    DOI10.1021/jp101999m
    AnnotationUltrafast excited-state dynamics of [Re(L)(CO)(3)(bpy)](n) (L = Cl, Br, n = 0; L = 4-ethyl-pyridine (Etpy), n = 1+; bpy = 2,2'-bipyridine) have been investigated in dimethylformamide (DMF) solution by fluorescence up-conversion (FIUC) and UV - vis transient absorption (TA) with similar to 100 is time,resolution. TA was also measured in the [1-ethyl-3-methyl-imidazolium]BF4 ionic liquid. The complexes show a very broad fluorescence band at 540-550 nm at zero time delay, which decays with 100-140 Is (depending on L) by intersystem crossing (ISC) to pi pi* intraligand ((IL)-I-3) and a Re(L)(CO)(3) -> bpy charge-transfer ((CT)-C-3) excited states. A second emission decay component (1.1-1.7 ps). apparent in the red part of the spectrum, is attributed to (IL)-I-3 -> (CT)-C-3 conversion, leaving phosphorescence from the lowest (CT)-C-3 state as the only emission signal at longer time delays. The triplet conversion is slower in DMF than acetonitrile, commensurate with solvation times.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2011
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