Journal
ORGANIC LETTERS
Volume 14, Issue 22, Pages 5696-5699Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol302710z
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- CNRS
- Ministere de l'Enseignement Superieur et de la Recherche
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The synthesis of unsymmetrical 3,5-dioligothienyl-BODIPY derivatives and their optical and redox properties are reported. The key step is the monobromination of the 2,6-dimethyl-3,5-dithienyl-BODIPY at the a position of the thiophene moiety. The additional thiophene modules are attached by palladium-catalyzed cross-coupling reactions. Increasing the number of modules on each side of the BODIPY core progressively shifts the absorption to 677 nm and the emission to 769 nm.
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