Substituent Controlled Tunable Fluorescence from Green to Red and pH Stimuli‐Induced Reversible Fluorescence Switching in Triphenylamine–Quinoxaline Derivatives

Abstract A series of triphenylamine‐quinoxaline donor‐acceptor (bipolar) compounds ( TPA‐QH , TPA‐QMe , TPA‐QCOOH and TPA‐QNO 2 ) with different substituents were synthesized and investigated their fluorescence properties, including stimuli‐induced fluorescence responses in solution and the solid‐state. Single crystal structural analysis revealed non‐planar molecular conformation, substituent controlled intermolecular interactions and molecular packing in the crystal lattice. TPA‐QH , TPA‐QMe , TPA‐QCOOH and TPA‐QNO 2 showed tunable solid‐state emission from green to red. TPA‐QH showed strong fluorescence at 487 nm (quantum yield (Φ f )=28.3 %) whereas NO 2 substituted TPA‐QNO 2 exhibited relatively weak fluorescence at 610 nm (Φ f =4.3 %). Density functional theoretical (DFT) calculations also indicated reduction of optical bandgap with substituting electron withdrawing group. The donor‐acceptor structure with intramolecular charge transfer (ICT) resulted solvent polarity dependent fluorescence tuning. The presence of acid responsive quinoxaline group was utilized to demonstrate pH‐responsive fluorescence switching and dual state fluorescence was utilized for fabricating rewritable fluorescent platform. Thus, the present study provides a structural insight to develop dual state emissive triphenylamine–quinoxaline based bipolar materials for optoelectronic applications.