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Immobilization and practical photoredox processes with dithienoquinoxaline

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F25%3A39923131" target="_blank" >RIV/00216275:25310/25:39923131 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.jcat.2025.116323" target="_blank" >https://doi.org/10.1016/j.jcat.2025.116323</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jcat.2025.116323" target="_blank" >10.1016/j.jcat.2025.116323</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Immobilization and practical photoredox processes with dithienoquinoxaline

  • Original language description

    A novel organic dithienoquinoxaline photoredox catalyst has been immobilized through a straightforward copolymerization approach. The performed heterogenization did not alter fundamental thermal, electrochemical, and optical properties and, most importantly, the ability of the excited catalyst to act either as a one-electron reductant or oxidant using a single light source (similar to 450 nm). The oxidation power of the triplet excited state of both homogeneous and heterogeneous photocatalysts has been demonstrated in the oxidation of sulphides, amines, and alcohols. The photoreduction of nitroaromatics and ketones has been accomplished by utilizing (double-excited) dithienoquinoxaline radical anion. Both oxidation and reduction reactions were accomplished either in batch (homo/heterogeneous) or under continuous-flow conditions using a porous flexible monolithic column with immobilized catalyst. Repetitive cyclic oxidation/reduction of pharmaceutically and industrially important fluorenol/one system along with a consecutive nitro reduction and sulphur oxidation in bis(4-nitrophenyl)sulphide towards an antimalarial agent further demonstrates the wide applicability of the developed catalytic systems/protocols. The recyclability and eventual structural changes of the immobilized catalyst have been addressed through FT-IR spectra and TON/TOF values.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA22-14988S" target="_blank" >GA22-14988S: DicyanoPyraZine: Versatile Tool for Photoredox Catalysis</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Catalysis

  • ISSN

    0021-9517

  • e-ISSN

    1090-2694

  • Volume of the periodical

    450

  • Issue of the periodical within the volume

    October 2025

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    116323

  • UT code for WoS article

    001556338400002

  • EID of the result in the Scopus database

    2-s2.0-105010878774