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  1. NázovTailoring photoisomerization pathways in donor-acceptor stenhouse adducts: The role of the hydroxy group
    Aut.údajeMichael M. Lerch, Miroslav Medveď ... [et al.]
    Autor Lerch Michael M. (10%)
    Spoluautori Medveď Miroslav 1971- (10%) UMBFP08 - Katedra chémie
    Lapini Andrea (10%)
    Laurent Adéle D. (10%)
    Iagatti Alessandro (5%)
    Bussotti Laura (5%)
    Szymański Wiktor (10%)
    Buma Wybren Jan (10%)
    Foggi Paolo (10%)
    Di Donato Mariangela (10%)
    Feringa Ben L. (10%)
    Zdroj.dok. The Journal of Physical Chemistry A. Vol. 122, no. 4 (2018), pp. 955-964. - Washington : The American Chemical Society, 2018
    Kľúč.slová chémia - chemistry   density functional theory  
    Form.deskr.články - journal articles
    Jazyk dok.angličtina
    KrajinaSpojené štáty
    Systematika 54
    URLhttps://pubs.acs.org/doi/abs/10.1021%2Facs.jpca.7b10255
    Kategória publikačnej činnosti ADC
    Číslo archívnej kópie44378
    Katal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Báza dátxpca - PUBLIKAČNÁ ČINNOSŤ
    OdkazyPERIODIKÁ-Súborný záznam periodika
    unrecognised

    unrecognised

    Názov
    Unsymmetrical benzothiazole-based dithienylethene photoswitches
    Aut.údaje
    Michelangelo Bovoloni ... [et al.]
    NázovUnsymmetrical benzothiazole-based dithienylethene photoswitches
    Aut.údajeMichelangelo Bovoloni ... [et al.]
    Autor Bovoloni Michelangelo (15%)
  2. TitleSolvent effects on the actinic step of donor-acceptor stenhouse adduct photoswitching
    Author infoMichael M. Lerch ... [et al.]
    Author Lerch Michael M. (15%)
    Co-authors Di Donato Mariangela (15%)
    Laurent Adéle D. (10%)
    Medveď Miroslav 1971- (10%) UMBFP08 - Katedra chémie
    Iagatti Alessandro (5%)
    Bussotti Laura (5%)
    Lapini Andrea (5%)
    Buma Wybren Jan (10%)
    Foggi Paolo (5%)
    Szymański Wiktor (10%)
    Feringa Ben L. (10%)
    Source document Angewandte Chemie : international edition : a journal of the German Chemical Society. Vol. 57, no. 27 (2018), pp. 8063-8068. - Weinheim : Wiley-VCH, 2018
    Keywords chémia - chemistry   solvent effects   density functional theory  
    Form. Descr.články - journal articles
    LanguageEnglish
    CountryGermany
    systematics 54
    URLLink na plný text
    Public work category ADC
    No. of Archival Copy44355
    Catal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Databasexpca - PUBLIKAČNÁ ČINNOSŤ
    ReferencesPERIODIKÁ-Súborný záznam periodika
    unrecognised

    unrecognised

  3. NázovShedding light on the photoisomerization pathway of donor-acceptor Stenhouse adducts
    Aut.údajeMariangela Di Donato, Michael M. Lerch ... [et al.]
    Autor Di Donato Mariangela (15%)
    Spoluautori Lerch Michael M. (15%)
    Lapini Andrea (5%)
    Laurent Adéle D. (10%)
    Iagatti Alessandro (5%)
    Bussotti Laura (5%)
    Ihrig Svante P. (5%)
    Medveď Miroslav 1971- (10%) UMBFP08 - Katedra chémie
    Jacquemin Denis (5%)
    Szymański Wiktor (5%)
    Buma Wybren Jan (10%)
    Foggi Paolo (5%)
    Feringa Ben L. (5%)
    Zdroj.dok. Journal of the American Chemical Society. Vol. 139, no. 44 (2017), pp. 15596-15599. - Washington : The American Chemical Society, 2017
    Kľúč.slová molekulové fotoprepínače - molecular photoswitches   donorno-akceptorové Stenhousove adukty   ultra-fast spectroscopy   DFT metóda  
    Jazyk dok.angličtina
    KrajinaSpojené štáty
    Systematika 54
    AnotáciaDonor-acceptor Stenhouse adducts (DASAs) are negative photochromes that hold great promise for a variety of applications. Key to optimizing their switching properties is a detailed understanding of the photoswitching mechanism, which, as yet, is absent. Here we characterize the actinic step of DASA-photoswitching and its key intermediate, which was studied using a combination of ultrafast visible and IR pump-probe spectroscopies and TD-DFT calculations. Comparison of the time-resolved IR spectra with DFT computations allowed to unambiguously identify the structure of the intermediate, confirming that light absorption induces a sequential reaction path in which a Z-E photoisomerization of C-2-C-3 is followed by a rotation around C-3-C-4 and a subsequent thermal cyclization step. First and second-generation DASAs share a common photoisomerization mechanism in chlorinated solvents with notable differences in kinetics and lifetimes of the excited states. The photogenerated intermediate of
    URLLink na plný text
    Kategória publikačnej činnosti ADC
    Číslo archívnej kópie41477
    Katal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Báza dátxpca - PUBLIKAČNÁ ČINNOSŤ
    OdkazyPERIODIKÁ-Súborný záznam periodika
    unrecognised

    unrecognised



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