Title
BODIPY dyads from a,c-biladiene salts
Document Type
Article
Publication Date
1-1-2017
Abstract
© 2017 The Royal Society of Chemistry. Asymmetric dimers of BODIPY dyes were synthesized from a,c-biladiene salts in good yields; this work constitutes a new versatile approach to the synthesis of BODIPY dyads, which display red-shifted absorptions and emissions in the visible spectral region, higher fluorescence quantum yields and larger Stokes shifts compared with monomeric BODIPYs. The X-ray structure of a 5,5′-dibromo-BODIPY dyad was obtained, and the reactivity of this compound under Suzuki cross-coupling reaction conditions was investigated.
Publication Source (Journal or Book title)
Organic and Biomolecular Chemistry
First Page
7255
Last Page
7257
Recommended Citation
Savoldelli, A., Paolesse, R., Fronczek, F., Smith, K., & Vicente, M. (2017). BODIPY dyads from a,c-biladiene salts. Organic and Biomolecular Chemistry, 15 (35), 7255-7257. https://doi.org/10.1039/c7ob01797a
