Abstract
A rapid, highly efficient and practically viable solid-solid melt reaction (SSMR) protocol has been developed for the synthesis of multi-colour-emissive quinoxaline-based small organic fluorophores (QBSOFs, 3) from readily available o-phenylenediamines (1) and α-bromoketones (2) or arylglyoxals/glyoxylic acids (4) under solvent- and catalyst-free conditions. This environmentally benign methodology features operational simplicity, avoidance of cost-intensive and scale-restrictive techniques such as microwave or ultrasonic irradiation, broad substrate compatibility with excellent functional-group tolerance, and a straightforward work-up affording products in high purity. Notably, the reactions proceed rapidly to deliver excellent to near-quantitative yields (95-99%). The successful gram-scale synthesis of 2-(4-chlorophenyl)quinoxaline (3a) further underscores the economic feasibility and industrial applicability of this approach for large-scale production of 2-arylquinoxalines. The solid-state photophysical properties of the synthesized quinoxaline fluorophores were systematically investigated. The compounds exhibit tunable solid-state emission spanning from purplish blue to the yellow light region, primarily governed by the nature of substituents at the 2-position of the quinoxaline core. Remarkably, compounds 4-(quinoxalin-2-yl)benzonitrile (3g) and 4-(6,7-dimethylquinoxalin-2-yl)benzonitrile (3u) display cold-white and warm-white light emission, respectively. Furthermore, the HOMO and LUMO energy levels are comparable to those of reported hole-transporting materials (HTMs), highlighting the dual luminescent and hole-transporting characteristics of these fluorophores. Consequently, these multi-colour-emissive QBSOFs, with intrinsic hole-transporting characteristics could be suitable for application in organic optoelectronic devices.