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• W4383819488 abstract "Small-molecule dyes that emit blue fluorescence, particularly those that emit in the S-blue region, are limited in number. Functionalization of benzene with electron-donating and -accepting groups generates single-benzene fluorophores (SBFs) with tunable emission properties. By exploring the unprecedented, interactive twin intramolecular H-bonds, a novel type of SBFs that exhibits several notable features for bioimaging applications is developed. Specifically, aniline derivatives bearing two carbonyl/carboxyl groups at ortho-positions have interactive H-bonds, which lead to conformational restriction, suppressed solvation, and increased HOMO-LUMO energy gaps from those of the conventional SBFs that have non-interactive H-bonds. The interactive H-bonds are manifested by notable photophysical properties among the new SBFs, such as S-blue emissive, bright, photo- and chemo-stable, solid-state-emissive, and environment (pH, polarity, and viscosity)-insensitive. The use of the highly faceted dye system to develop a reliable fluorescent probe, organelle-staining dyes, and a fluorescence-resonance-energy-transfer probe for hydrogen sulfide demonstrates its potential in bioimaging applications." @default.
• W4383819488 created "2023-07-11" @default.
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• W4383819488 date "2023-07-09" @default.
• W4383819488 modified "2023-10-01" @default.
• W4383819488 title "Interactive Twin Intramolecular Hydrogen Bonds Enable Bright, <i>S</i>‐Blue Emissive, Environment‐Insensitive Single‐Benzene Fluorophores" @default.
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• W4383819488 doi "https://doi.org/10.1002/adfm.202304507" @default.
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