Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270827 | Tetrahedron Letters | 2010 | 4 Pages |
A new internal charge transfer probe, NAPH-1, synthesized by incorporating photoemitive naphthalimide core with an acidic imidazolium ring, offers highly selective colorimetric and ratiometric 'off-on' signaling for targeting Fâ, while Clâ, Brâ, Iâ, HSO4-, SCNâ, AcOâ, and NO3- do not appreciably perturb the photophysical properties of the probe even at relatively higher concentrations than the Fâ. Deprotonation of the imidazolium ring, supported by the 1H NMR and theoritical studies, seems to cause the spectral modulations.
Graphical abstractA new internal charge transfer probe, NAPH-1, offers selective colorimetric and ratiometric 'off-on' signaling for targeting Fâ, while Clâ, Brâ, Iâ, HSO4-, SCNâ, AcOâ, and NO3- do not appreciably perturb the photophysical properties of the probe even at relatively higher concentration than Fâ.Download full-size image