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

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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Bibliographische Detailangaben
Veröffentlicht in:	Chemical communications (Cambridge, England) England), 2011-10, Vol.47 (37), p.10425-10427
Hauptverfasser:	Vives, Guillaume, Giansante, Carlo, Bofinger, Robin, Raffy, Guillaume, Del Guerzo, André, Kauffmann, Brice, Batat, Pinar, Jonusauskas, Gediminas, McClenaghan, Nathan D
Format:	Artikel
Sprache:	eng
Schlagworte:	Amines - chemistry Boron Compounds - chemistry Fluorescent Dyes - chemistry Hydrocarbons, Fluorinated - chemistry Optics Physics Spectrometry, Fluorescence Sulfhydryl Compounds - chemistry
Online-Zugang:	Volltext
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Beschreibung
Zusammenfassung:	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.
ISSN:	1359-7345 1364-548X
DOI:	10.1039/c1cc13778f