Halogenated azobenzene acrylates: from efficient solution photoswitching to stable solid-state photochromic materials

The design, synthesis, and comprehensive characterization of six novel halogenated azobenzene acrylate monomers bearing fluorine, chlorine or bromine substituents is reported. The monomers were prepared via a facile three-step synthetic route involving azo-coupling, O- alkylation and O -acylation. Apart from the steady electrochemical properties, halogen substitution proved to be a very useful tool to tune the thermal and optical properties, light-induced switching in particular. Monohalogen derivatives exhibited up to 93% E → Z photoconversion efficiency in solution, whereas the efficiency of dihalogen analogues is lower by 20%, which is ascribed to their nonplanar arrangement. Kinetics studies identified the most stable Z -isomer of the difluoro derivative ( τ 1/2 = 3.74/6.59 h at 60 °C in DCE/CDCl 3 ). The monofluoro derivative embedded in a polystyrene film demonstrated photoresponsive behavior and remarkable stability by maintaining a macroscopically visible color change for over 90 days. These findings demonstrate that ortho -halogenation is a powerful tool for tuning the properties of photoresponsive materials for potential applications in colorimetric thermal sensing and light-controlled functional systems.