Abstract

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 F −, while Cl −, Br −, I −, HSO 4 - , SCN −, AcO −, and NO 3 - do not appreciably perturb the photophysical properties of the probe even at relatively higher concentrations than the F −. Deprotonation of the imidazolium ring, supported by the 1H NMR and theoritical studies, seems to cause the spectral modulations.

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