Theoretical Investigations on the Excited-State Dynamics of an Al3+ Fluorescence Sensor.

Twisted internal charge transfer (TICT) states are of fundamental importance during the photo-physical processes of dyes and sensors. In this contribution, excited-state dynamics of an Al3+ fluorescence sensor 1-{[(2-hydroxyphenyl)-imino]methyl}naphthalen-2-ol based on the turn-on signal is clarified. Two different dark TICT states are observed by exploring the excited-state potential energy surface. With the twist of the C2-N bond, the two dark states can be reached facilely, which induce the experimentally observed weak fluorescence of the sensor. The sensing mechanism is then uncovered by investigating the electronic coupling between the sensor and analyte. Al3+ is proved to form strong coordination bonds with the sensor, which restricts the motion of the C2-N bond. Consequently, the TICT states are eliminated, which generate the turn-on signal. This sensing mechanism is trustworthy and intrinsically different from the previously proposed one, which would shed some light on the design of turn-on sensors.