Blue-orange emitting carbazole based donor-acceptor derivatives: Synthesis and studies of modulating acceptor unit on opto-electrochemical and theoretical properties.

[Display omitted] • Carbazole based Donor–Acceptor derivatives are synthesized. • ICT transition and emission varied with modulation in acceptor units. • Excellent solvatofluorochromism with "Blue to orange" emission in solution and solid state exhibit by dyes. • Some dyes possess outstanding AIE properties by stable emissive nanoparticles formation. • Dyes offers electron transporting characteristics and small ΔE ST. In order to demonstrate an effect of varying acceptor unit on optoelectronic properties of Donor–Acceptor (D–A) assembly, we herein designed and synthesized C–N coupled, carbazole based dyes 1 – 8 by employing Buchwald–Hartwig coupling amination reaction and fully characterized by spectroscopic methods. Presence of intramolecular charge transfer (ICT) transitions (λ max = 403–467 nm) in absorption spectra of all dyes reminiscent D–A assembly in it and emit in blue–yellow region (λ emm = 467–565 nm) in solution state with marked positive solvatochromism. The photophysical studies of some of the dyes in different THF/water mixtures revealed aggregation-induced emission (AIE) feature with the nanoparticles formation, as confirmed by dynamic light scattering (DLS) technique. The HOMO (−5.42 to −5.74 eV) and LUMO (−3.03 to −3.50 eV) energy level of these molecules measured by cyclic voltammetry suggest electron transporting property in it. Further, DFT/TDDFT calculation of dyes, indicate quite comparable theoretical and experimental photophysical and electrochemical data. Moreover, calculated singlet (S 1) and triplet (T 1) excitation energy levels by DFT/B3LYP/6–311 G+(d,p) shows small ΔE ST value for some dyes and hence called as TADF emitters. Thus obtained all optoelectrochemical properties of dyes propose its potential use in optoelectronic devices and in biosensing. [ABSTRACT FROM AUTHOR]