Temperature-Controlled Locally Excited and Twisted Intramolecular Charge-Transfer State-Dependent Fluorescence Switching in Triphenylamine-Benzothiazole Derivatives.

Abstract

Triphenylamine–benzothiazole derivatives, N-(4-(benzo[d]thiazol-2-yl)phenyl)-N-phenylbenzenamine (1), N-(4-(benzo[d]thiazol-2-yl)-3-methoxyphenyl)-N-phenylbenzenamine (2), and 2-(benzo[d]thiazol-2-yl)-5-(diphenylamino)phenol (3), showed unusual temperature-controlled locally excited (LE) and twisted intramolecular charge-transfer (TICT) state fluorescence switching in polar solvents. The detailed photophysical studies (absorption, fluorescence, lifetime, and quantum yield) in various solvents confirmed polarity-dependent LE and TICT state formation and fluorescence tuning. 1 and 2 exhibited strong fluorescence with short lifetime in nonpolar solvents compared to polar solvents. 1, 2, and 3 in dimethylformamide (DMF) at room temperature showed low-energy weak TICT state fluorescence, whereas high-energy strong LE state fluorescence was observed at −196 °C. Interestingly, further increasing the temperature from 20 to 100 °C, the DMF solution of 1 and 2 exhibited rare fluorescence enhancement with a slight blue shift of λmax via activating more vibrational bands of the TICT state. Thus, 1 and 2 showed weak TICT state fluorescence at room temperature, strong LE state fluorescence at −196 °C, and activation of TICT state at 100 °C. Moreover, molecular conformation and aggregation in the solid state influenced strongly on the fluorescence properties of 1, 2, and 3. Solid-state fluorescence and pH-responsive imidazole nitrogen have been exploited for demonstrating halochromism-induced fluorescence switching. Computational studies provided further insights into the fluorescence tuning and switching. The present studies provide understanding and opportunity to make use of D–A organic molecules in the LE and TICT states for achieving fluorescence switching and tuning.