2,3-Diarylmaleate salts as a versatile class of diarylethenes with a full spectrum of photoactivity in water.

There is incessant interest in the transfer of common chemical processes from organic solvents to water, which is vital for the development of bioinspired and green chemical technologies. Diarylethenes feature a rich photochemistry, including both irreversible and reversible reactions that are in demand in organic synthesis, materials chemistry, and photopharmacology. Herein, we introduce the first versatile class of diarylethenes, namely, potassium 2,3-diarylmaleates (DAMs), that show excellent solubility in water. DAMs obtained from highly available precursors feature a full spectrum of photoactivity in water and undergo irreversible reactions (oxidative cyclization or rearrangement) or reversible photocyclization (switching), depending on their structure. This finding paves a way towards wider application of diarylethenes in photopharmacology and bioinspired technologies that require aqueous media for photochemical reactions.

Redirecting of Charge Transfer Enables the Control of the Photoactivity of Terarylenes.

Photoinduced charge transfer affects the efficiency and selectivity of photochemical reactions. Incorporation of donating groups into the isoquinolinium core allowed us to overcome the photochemical inactivity of the corresponding dithienyl-substituted terarylenes, presumably by redirecting the charge transfer within the molecule, and gave access to a new family of thermally reversible photoswitches.