ArticleNature communications2026
Highly luminescent carbazole-functionalized tris(tribromophenyl)methyl radicals with stable circularly polarized photoluminescence.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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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Who cites it
1 citing paper in PubMed.
- Luminescent Donor-Acceptor Radical With Propeller Chirality: Bright and Photostable Red Circularly Polarized Luminescence and Whispering Gallery Mode Resonance.Angewandte Chemie (International ed. in English) · 2026Article
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Authors and funding
9 authors.
Funding
Abstract
Brominated trityl radicals form stable enantiomers and present promising candidates for molecular qubits in spintronic and quantum technologies. However, their inherently weak photoluminescence (ϕ < 3 %) limits optical spin readout. Here, we report the synthesis of three carbazole-functionalized tris(2,4,6-tribromophenyl)methyl (TTBrM) radicals via Buchwald-Hartwig cross-coupling. These chiral open-shell emitters exhibit high photoluminescence quantum yields of up to ϕ = 72%, comparable to their chlorinated analogues, with red-shifted emission (λ
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Registered trials
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