| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5272908 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Mono- and bis-NTA-BODIPY dyes have been efficiently synthesized by amide bond formation between hepta-alkylated meso-aryl-BODIPY derivatives and the free amine of mono- and bis-NTA binder surrogates. These new fluorescent hybrids exhibited valuable photophysical properties under buffered aqueous conditions, thus expanding the arsenal of water-soluble BODIPY dyes for potential labeling and monitoring of biological systems and processes.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Marie Brellier, Guy Duportail, Rachid Baati,