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• W2771202345 abstract "Abstract In recent years, nonconjugated, fluorophore‐free organic polymers have emerged as potentially useful light‐emitting materials. The fluorescence properties of a novel class of nonconjugated, tert ‐butyl carboxylate functionalized stilbene‐containing alternating copolymers are investigated in this work. These sterically crowded, semi‐rigid copolymers exhibit very strong blue fluorescence in organic solvents upon irradiation. The origin of the fluorescent band with high quantum yield is attributed to the “through space” π–π interactions between the phenyl rings from the stilbene and CO groups from the anhydride groups. To the best of our knowledge, the di‐ tert ‐butyl group‐containing stilbene and maleic anhydride alternating copolymer showed one of the highest fluorescent intensities among all fluorophore‐free polymers. The excellent linearity of the luminescence property of this copolymer is an important attribute for future potential quantitative applications. The fluorescence is maintained when the tert ‐butyl groups are removed and the resulting carboxylic acid‐functionalized copolymer is dissolved in water at neutral pH, which can render these copolymers as attractive candidates for diagnostic and therapeutic applications." @default.
• W2771202345 created "2017-12-22" @default.
• W2771202345 creator A5020527784 @default.
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• W2771202345 date "2017-12-06" @default.
• W2771202345 modified "2023-10-15" @default.
• W2771202345 title "Enhanced Fluorescence Properties of Stilbene‐Containing Alternating Copolymers" @default.
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• W2771202345 doi "https://doi.org/10.1002/marc.201700530" @default.
• W2771202345 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29210511" @default.
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