ArticleChemical science2025
Photo-generated radical mediated molecular luminescence enhancement.
Article in Chemical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Corrections and comments
- Retracted
Authors and funding
7 authors.
Funding
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Abstract
Achieving rapid modulation of molecular luminescence under external stimuli remains a significant challenge in organic luminescent materials. Herein, we present a radical-mediated approach to achieve dynamic fluorescence switching. A series of benzil derivatives (BS, BZ, BD, and BQ) exhibit rapid transitions from nearly non-luminescent states to highly fluorescent states under continuous ultraviolet (UV) irradiation in solution. Notably, the absolute photoluminescence quantum yield of BS solution increased 41-fold, from 1.26% to 51.09%, after 330 s of 365 nm UV exposure. Mechanistic investigations reveal that this unique luminescence enhancement originates from UV-induced generation of aromatic carbonyl radicals. In general, molecules in solution undergo photodegradation with increasing irradiation time, resulting in a decrease in luminescence intensity. In contrast, we report a molecule whose luminescence intensity increases with increasing irradiation time, which is very rare. This work not only advances the mechanistic understanding of stimuli-responsive luminescence but also opens a new avenue for designing smart organic materials with tailored optoelectronic functionalities.
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Registered trials
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