Univ. Bordeaux, ISM, CNRS UMR 5255, F-33400 Talence, France.
Chem Commun (Camb). 2011 Oct 7;47(37):10425-7. doi: 10.1039/c1cc13778f. Epub 2011 Aug 19.
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.
使用烷硫醇或伯胺对包含 BODIPY 荧光团的全氟苯基单元进行选择性亲核取代，提供了一种定量荧光团标记策略，同时保持了高光稳定性和接近 unity 的发射量子产率。
