Issue 37, 2011
From the journal:

Chemical Communications

Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates†

Guillaume Vives,a   Carlo Giansante,a   Robin Bofinger,a   Guillaume Raffy,a   André Del Guerzo,*a   Brice Kauffmann,b   Pinar Batat,ac   Gediminas Jonusauskasc  and  Nathan D. McClenaghan*a  

* Corresponding authors

a Univ. Bordeaux, ISM, CNRS UMR 5255, F-33400 Talence, France
E-mail: n.mc-clenaghan@ism.u-bordeaux1.fr, a.del-guerzo@ism.u-bordeaux1.fr

b Univ. Bordeaux, IECB, CNRS UMS 3033, F-33607 Pessac, France

c Univ. Bordeaux, LOMA, CNRS UMR 5798, F-33400 Talence, France

Abstract

Selective nucleophilic substitution on a perfluorophenyl unit comprising a BODIPY fluorophore using an alkanethiol or a primary amine offers a quantitative fluorophore labelling strategy, while retaining high photostability and emission quantum yields approaching unity.

Graphical abstract: Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates

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Article information

DOI
https://doi.org/10.1039/C1CC13778F
Article type
Communication
Submitted
24 Jun 2011
Accepted
07 Aug 2011
First published
19 Aug 2011

Chem. Commun., 2011,47, 10425-10427

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Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates

G. Vives, C. Giansante, R. Bofinger, G. Raffy, A. D. Guerzo, B. Kauffmann, P. Batat, G. Jonusauskas and N. D. McClenaghan, Chem. Commun., 2011, 47, 10425 DOI: 10.1039/C1CC13778F

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