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Issue 37, 2011
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Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates

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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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Publication details

The article was received on 24 Jun 2011, accepted on 07 Aug 2011 and first published on 19 Aug 2011


Article type: Communication
DOI: 10.1039/C1CC13778F
Citation: 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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