articleTop 10% cited
Palladium‐Catalyzed Coupling Reactions for the Functionalization of BODIPY Dyes with Fluorescence Spanning the Visible Spectrum
European Journal of Organic Chemistry · 2006 · Vol. 2006(20) · pp. 4658–4663
Abstract
Abstract 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 BODIPY derivatives range from green to near‐infrared. The new class of ethynylaryl‐substituted BODIPY dyes are extremely bright fluorescent compounds.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
Luminescence and Fluorescent MaterialsNanoplatforms for cancer theranosticsMolecular Sensors and Ion DetectionBODIPYChemistryFluorophoreSonogashira couplingPhotochemistryFluorescencePalladiumArylStille reactionSuzuki reaction
Funding
- Fonds Wetenschappelijk Onderzoek
- Vlaamse regering
Citations
255
FWCI
7.62
field-weighted impact
References
46
Percentile
98%
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