Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202311224
Keywords
Cyanines; Cyclic Peptides; Fluorescent Materials; Photoisomerization; Supramolecular Chemistry
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In this study, a simple supramolecular strategy was developed to address the long-standing challenges associated with cyanine dyes, resulting in the development of ultrabright cyanine-based fluorescent materials. Through the incorporation of cyanine moieties in a cyclic peptide-based supramolecular scaffold, the resulting supra-cyanines exhibited high fluorescence quantum yields, providing a versatile approach for constructing highly emissive cyanine-based supramolecular materials.
Fluorescent materials with high brightness play a crucial role in the advancement of various technologies such as bioimaging, photonics, and OLEDs. While significant efforts are dedicated to designing new organic dyes with improved performance, enhancing the brightness of existing dyes holds equal importance. In this study, we present a simple supramolecular strategy to develop ultrabright cyanine-based fluorescent materials by addressing long-standing challenges associated with cyanine dyes, including undesired cis-trans photoisomerization and aggregation-caused quenching. Supra-cyanines are obtained by incorporating cyanine moieties in a cyclic peptide-based supramolecular scaffold, and exhibit high fluorescence quantum yields (up to 50 %) in both solution and in the solid state. These findings offer a versatile approach for constructing highly emissive cyanine-based supramolecular materials. A supramolecular approach has been developed to inhibit the undesired cis-trans photoisomerization and aggregation-caused quenching of cyanine dyes. By utilizing a cyclic peptide-based supramolecular scaffold, the resulting supra-cyanines exhibit high fluorescence quantum yields in both solution and in the solid state.image
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