Controlling emissive behaviour through molecular design: 2,3-bis(2,5-dimethylthiophen-3-yl)quinoxalines with variable fluorene substitution

Abstract

We report a new family of donor–acceptor–donor (D–A–D) chromophores based on 2,3-bis(2,5-dimethyl thiophen-3-yl)quinoxaline, where the electronic and steric environment is tuned through fluorene substituents at the 5,8-positions. Variation of the 9,9-substituents (aryl, branched alkyl, and spiro-linked groups) enables systematic modulation of solubility, conformational rigidity, and intermolecular interactions while preserving the electron-deficient quinoxaline core. All synthesized derivatives (DMTQ1–DMTQ5) exhibit characteristic p–p* absorption around 380 nm and broad intramolecular charge-transfer (ICT) emission in solution (490–502 nm) with photoluminescence quantum yields up to 45% and lifetimes of 2.7–4.0 ns. A detailed solvatochromic and time-resolved study of DMTQ5 confirmed strong ICT character, manifested by red-shifted emission and polarity-dependent lifetime shortening. Electrochemical studies reveal consistent oxidation onsets (0.54–0.64 V vs. Fc/Fc+), corresponding to HOMO levels of 5.34 to 5.44 eV, while LUMO energies ( 2.57 to 2.67 eV) were derived from optical gaps of B2.8 eV. In the solid state, spin-coated films of selected derivatives exhibit pronounced photochromic switching of emission colour and intensity, a behaviour absent in solution and directly demonstrated using UV-LED excitation. These results establish fluorene substitution as a versatile strategy to direct emissive behaviour in quinoxaline-based chromophores, highlighting their potential as polarity-sensitive probes, light-responsive coatings, and optoelectronic materials.