Jump to main content
Jump to site search


BODIPY dyads from a,c-biladiene salts

Abstract

Asymmetric dimers of BODIPY dyes were synthesized from a,c-biladienes 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.

Back to tab navigation

Supplementary files

Publication details

The article was received on 20 Jul 2017, accepted on 11 Aug 2017 and first published on 11 Aug 2017


Article type: Communication
DOI: 10.1039/C7OB01797A
Citation: Org. Biomol. Chem., 2017, Accepted Manuscript
  •   Request permissions

    BODIPY dyads from a,c-biladiene salts

    A. Savoldelli, R. Paolesse, F. R. Fronczek, K. M. Smith and M. G. H. Vicente, Org. Biomol. Chem., 2017, Accepted Manuscript , DOI: 10.1039/C7OB01797A

Search articles by author

Spotlight

Advertisements