Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates
BATAT, Pinar
Institut des Sciences Moléculaires [ISM]
Laboratoire Ondes et Matière d'Aquitaine [LOMA]
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Institut des Sciences Moléculaires [ISM]
Laboratoire Ondes et Matière d'Aquitaine [LOMA]
Language
en
Article de revue
This item was published in
Chemical Communications. 2011-10-07, vol. 47, n° 37, p. 10425-10427
Royal Society of Chemistry
English 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 ...Read more >
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.Read less <
European Project
Communication between Functional Molecules using Photocontrolled Ions
Origin
Hal imported