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.
Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates
GIANSANTE, CARLO;
2011-01-01
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.File in questo prodotto:
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