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. © 2011 The Royal Society of Chemistry.
Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: Photostable thiol and amine conjugates
Giansante C.;
2011
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. © 2011 The Royal Society of Chemistry.File in questo prodotto:
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Chemical Communications, 2011, 47 (37) 10425-10427.pdf
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