Experimental and Computational Optoelectrochemical Investigation of Quinoxaline Based Charge Transfer Derivatives: Green‐Orange Emissive, AIEE Active Materials

2,3-Diphenylquinoxalin-6-yl based dyes were synthesized and characterized using 1H, 13C, HRMS and NOSEY spectroscopic technique. The comprehensive photophysical, aggregation-induced emission enhancement (AIEE) activity, electrochemical and theoretical studies of dyes explored. The intramolecular charge transfer transition (ICT) at 380-386 nm in absorption spectra suggest weak push-pull feature of dyes. Dyes show emission in green to orange region (λmax: 561-588 nm) in solvent as well as solid state. The Stokes shift of dyes is 7979-9167 cm-1. The minimal positive solvatochromism (slight variation in λemi) own by dyes, suggest environment stability of dyes in various solvent polarity. AIEE activity with good emission at solid-state make the dyes suitable candidature for solid state OLED's application. Further Dynamic Light Scattering (DLS) studies of dye 1 validate reverse correlation of emission behavior of nanoaggregate formed at high water fraction of THF-H2O mixture with its particle size. The good thermal stability of dyes reflected by decomposition temperature i.e., 221°C-357°C (292°C-372°C) for 5(10)% weight loss. The LUMO (-3.68 to -3.83 eV) of derivatives are lower than LUMO of reported n-type materials (-3.0 to -3.30 eV). Thus, photophysical with AIEE activity and electrochemical properties obtained for dyes signify suitability of it in organic electronics.