Počet záznamů: 1  

Central Ring Puckering Enhances the Stokes Shift of Xanthene Dyes

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    0583934 - ÚOCHB 2025 RIV DE eng J - Článek v odborném periodiku
    Dunlop, David - Horváth, P. - Klán, P. - Slanina, Tomáš - Šebej, P.
    Central Ring Puckering Enhances the Stokes Shift of Xanthene Dyes.
    Chemistry - A European Journal. Roč. 30, č. 19 (2024), č. článku e202400024. ISSN 0947-6539. E-ISSN 1521-3765
    Grant CEP: GA MŠMT(CZ) LTC20076
    Výzkumná infrastruktura: RECETOX RI II - 90269
    Institucionální podpora: RVO:61388963
    Klíčová slova: conformation * fluorescence * functional dyes * pyronin * quantum chemical calculations * stokes shift * xanthene
    Obor OECD: Physical chemistry
    Impakt faktor: 4.3, rok: 2022
    Způsob publikování: Open access
    https://doi.org/10.1002/chem.202400024

    Small-molecule dyes are generally designed based on well-understood electronic effects. However, steric hindrance can promote excited-state geometric relaxation, increasing the difference between the positions of absorption and emission bands (the Stokes shift). Accordingly, we hypothesized that sterically induced central ring puckering in xanthene dyes could be used to systematically increase their Stokes shift. Through a combined experimental/quantum-chemical approach, we screened a group of (9-acylimino)-pyronin dyes with a perturbed central ring geometry. Our results showed that an atom with sp(3) hybridization in position 10 of (9-acylimino)-pyronins induces central ring puckering and facilitates excited-state geometric relaxation, thereby markedly enhancing their Stokes shifts (by up to similar to 2000 cm(-1)). Thus, we prepared fluorescent (9-acylimino)-pyronin pH sensors, which showed a Stokes shift disparity between acid and base forms of up to similar to 8700 cm(-1). Moreover, the concept of ring puckering-enhanced Stokes shift can be applied to a wide range of xanthene analogues found in the literature. Therefore, central ring puckering may be reliably used as a strategy for enhancing Stokes shifts in the rational design of dyes.
    Trvalý link: https://hdl.handle.net/11104/0351920

     
     
Počet záznamů: 1  

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