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  1. TitleMechanistic basis for red light switching of azonium lons
    Author infoMiroslav Medveď ... [et al.]
    Author Medveď Miroslav 1971- (13%) UMBFP08 - Katedra chémie
    Co-authors Di Donato Mariangela (13%)
    Buma Wybren Jan (10%)
    Laurent Adéle D. (10%)
    Lameijer Lucien N. (5%)
    Hrivnák Tomáš (7%)
    Romanov Ivan (5%)
    Tran Susannah (5%)
    Feringa Ben L. (5%)
    Szymanski Wiktor (10%)
    Woolley G. Andrew (17%)
    Source document Journal of the American Chemical Society. Vol. 145, no. 36 (2023), pp. 19894-19902. - Washington : The American Chemical Society, 2023
    Keywords svetlo   ióny   chemické výpočty   chemické zlúčeniny - chemical compounds  
    Form. Descr.články - journal articles
    LanguageEnglish
    CountryUnited States of America
    URLLink na zdrojový dokument
    Public work category ADC
    No. of Archival Copy53514
    Catal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Databasexpca - PUBLIKAČNÁ ČINNOSŤ
    ReferencesPERIODIKÁ-Súborný záznam periodika
  2. TitleTailoring the optical and dynamic properties of iminothioindoxyl photoswitches through acidochromism
    Author infoMiroslav Medved', Mark W. H. Hoorens ... [et al.]
    Author Medveď Miroslav 1971- (10%) UMBFP08 - Katedra chémie
    Co-authors Hoorens Mark W. H. (10%)
    Di Donato Mariangela (10%)
    Laurent Adéle D. (10%)
    Fan Jiayun (10%)
    Taddei Maria (10%)
    Hilbers Michiel (10%)
    Feringa Ben L. (10%)
    Buma Wybren Jan (10%)
    Szymanski Wiktor (10%)
    Source document Chemical Science. Vol. 12, no. 12 (2021), pp. 4588-4598. - Cambridge : Royal Society of Chemistry, 2021
    Keywords nelineárne optické vlastnosti   fotoprepínače - photoswitches  
    Form. Descr.články - journal articles
    LanguageEnglish
    CountryGreat Britian
    URLLink na plný text
    Public work category ADC
    No. of Archival Copy51137
    Catal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Databasexpca - PUBLIKAČNÁ ČINNOSŤ
    ReferencesPERIODIKÁ-Súborný záznam periodika
  3. TitleIminothioindoxyl as a molecular photoswitch with 100 nm band separation in the visible range
    Author infoMark W. H. Hoorens ... [et al.]
    Author Hoorens Mark W. H. (20%)
    Co-authors Medveď Miroslav 1971- (10%) UMBFP08 - Katedra chémie
    Laurent Adéle D. (10%)
    Di Donato Mariangela (10%)
    Fanetti Samuele (5%)
    Slappendel Laura (5%)
    Hilbers (5%)
    Feringa Ben L. (10%)
    Buma Wybren Jan (10%)
    Szymański Wiktor (15%)
    Source document Nature Communications. Vol. 10, no. 2390 (2019), pp. 1-11. - London : Nature Research, 2019
    Keywords molekulové fotoprepínače - molecular photoswitches   teória funkcionálu hustoty   chémia - chemistry   prírodné vedy - natural sciences   fotochemické reakcie - photochemical reactions  
    Form. Descr.články - journal articles
    LanguageEnglish
    CountryGreat Britian
    AnnotationLight is an exceptional external stimulus for establishing precise control over the properties and functions of chemical and biological systems, which is enabled through the use of molecular photoswitches. Ideal photoswitches are operated with visible light only, show large separation of absorption bands and are functional in various solvents including water, posing an unmet challenge. Here we show a class of fully-visible-light-operated molecular photoswitches, lminothioindoxyls (ITIs) that meet these requirements. ITIs show a band separation of over 100 nm, isomerize on picosecond time scale and thermally relax on millisecond time scale. Using a combination of advanced spectroscopic and computational techniques, we provide the rationale for the switching behavior of ITIs and the influence of structural modifications and environment, including aqueous solution, on their photochemical properties. This research paves the way for the development of improved photo-controlled systems for a
    Public work category ADC
    No. of Archival Copy47137
    Catal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Databasexpca - PUBLIKAČNÁ ČINNOSŤ
    ReferencesPERIODIKÁ-Súborný záznam periodika
    unrecognised

    unrecognised

  4. 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

  5. TitleTailoring photoisomerization pathways in donor-acceptor stenhouse adducts: The role of the hydroxy group
    Author infoMichael M. Lerch, Miroslav Medveď ... [et al.]
    Author Lerch Michael M. (10%)
    Co-authors 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%)
    Source document The Journal of Physical Chemistry A. Vol. 122, no. 4 (2018), pp. 955-964. - Washington : The American Chemical Society, 2018
    Keywords chémia - chemistry   density functional theory  
    Form. Descr.články - journal articles
    LanguageEnglish
    CountryUnited States of America
    systematics 54
    URLhttps://pubs.acs.org/doi/abs/10.1021%2Facs.jpca.7b10255
    Public work category ADC
    No. of Archival Copy44378
    Catal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Databasexpca - PUBLIKAČNÁ ČINNOSŤ
    ReferencesPERIODIKÁ-Súborný záznam periodika
    unrecognised

    unrecognised

  6. TitleShedding light on the photoisomerization pathway of donor-acceptor Stenhouse adducts
    Author infoMariangela Di Donato, Michael M. Lerch ... [et al.]
    Author Di Donato Mariangela (15%)
    Co-authors 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%)
    Source document Journal of the American Chemical Society. Vol. 139, no. 44 (2017), pp. 15596-15599. - Washington : The American Chemical Society, 2017
    Keywords molekulové fotoprepínače - molecular photoswitches   donorno-akceptorové Stenhousove adukty   ultra-fast spectroscopy   DFT metóda  
    LanguageEnglish
    CountryUnited States of America
    systematics 54
    AnnotationDonor-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
    Public work category ADC
    No. of Archival Copy41477
    Catal.org.BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici
    Databasexpca - PUBLIKAČNÁ ČINNOSŤ
    ReferencesPERIODIKÁ-Súborný záznam periodika
    unrecognised

    unrecognised



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