2011Chemical CommunicationsRequires access

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

Guillaume Vives, Carlo Giansante, Robin Bofinger, Guillaume Raffy, André Del Guerzo, Brice Kauffmann, Pınar Batat, Gediminas Jonušauskas, Nathan D. McClenaghan

Open publisher page 49 citations

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.

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What this paper is about

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.

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OpenAlex reports 49 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available 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.

Key concepts: Fluorophore, BODIPY, Amine gas treating, Thiol, Fluorescence, Chemistry, Conjugate, Photochemistry

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