4.5 Article

Palladium-catalyzed coupling reactions for the functionalization of BODIPY dyes with fluorescence spanning the visible spectrum

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EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2006, 期 20, 页码 4658-4663

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200600531

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fluorescent dyes; palladium-catalyzed reactions; BODIPY compounds; UV; vis spectroscopy; fluorescence; spectroscopy

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The BODIPY fluorophore can easily be functionalized at the 3- (and 5-)position(s) with one or two aryl, ethenylaryl and ethynylaryl moieties by palladium-catalyzed coupling reactions of the 3,5-dichloroBODIPY derivative using the Stille, Suzuki, Heck and Sonogashira reactions. The fluorescence excitation and emission spectral maxima of the novel BOD-JPY derivatives range from green to near-infrared. The new class of ethynylaryl-substituted BODIPY dyes are extremely bright fluorescent compounds. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006).

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