| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276461 | Tetrahedron Letters | 2008 | 4 Pages |
A new fluorescent probe 1, N-butyl-4, 5-(p-aldehyde)phenyl-1,8-naphthalimide, was designed and synthesized for the determination of the cysteine (Cys). Upon addition of Cys, the emission of 1 was enhanced with about 25Â nm red-shift in the emission maximum (from 455 to 480Â nm), accompanied with the fluorescent color change from blue to cyan, which was attributed to the reaction of the aldehyde groups in 1 with cysteine to form very stable thiazolidines derivative. Compound 1 was highly selective for cysteine detection without the interference of other amino acids and can be used for bioimaging of Cys.
Graphical abstractAn aqueous soluble fluorophore chemosensor 1 for recognition of Cys was designed and synthesized easily, and it displays high selectivity for Cys by fluorometric enhancement with red-shift in aqueous solution. It displays high selectivity for Cys by fluorometric enhancement with red-shift in aqueous solution without the interference of other amino acids. Moreover, fluorescence images indicate that 1 can be used for bioimaging of Cys in living cell.Download full-size image
