Towards low-energy-light-driven bistable photoswitches: ortho-fluoroaminoazobenzenes

Thermally stable photoswitches that are driven with low-energy light are rare, yet crucial for extending the applicability of photoresponsive molecules and materials towards, e.g., living systems. Combined ortho-fluorination and -amination couples high visible light absorptivity of o-aminoazobenzenes with the extraordinary bistability of o-fluoroazobenzenes. Herein, we report a library of easily accessible o-aminofluoroazobenzenes and establish structure-property relationships regarding spectral qualities, visible light isomerization efficiency and thermal stability of the cis-isomer with respect to the degree of o-substitution and choice of amino substituent. We rationalize the experimental results with quantum chemical calculations, revealing the nature of low-lying excited states and providing insight into thermal isomerization. The synthesized azobenzenes absorb at up to 600 nm and their thermal cis-lifetimes range from milliseconds to months. The most unique example can be driven from trans to cis with any wavelength from UV up to 595 nm, while still exhibiting a thermal cis-lifetime of 81 days. [GRAPHICS] .

Automated summary

In this study, a library of easily accessible o-aminofluoroazobenzenes was synthesized and their structure-property relationships regarding spectral qualities, visible light isomerization efficiency, and thermal stability were established. The experimental results were rationalized with quantum chemical calculations, providing insight into the nature of low-lying excited states and thermal isomerization. The synthesized azobenzenes exhibited absorption at up to 600 nm and thermal cis-lifetimes ranging from milliseconds to months.