Phenolylazoindole scaffold for facilely synthesized and bis-functional photoswitches combining controllable fluorescence and antifungal properties using theoretical methods.

Functionalization is a major challenge for the application of photoswitches. With the aim to develop novel bis-functional azo photoswitches with stationary photophysical properties, a series of phenolylazoindole derivatives were designed, synthesized, and characterized NMR spectroscopy studies and high-resolution mass spectrometry (HRMS). Herein, UV/Vis and H NMR spectra revealed that the photostationary state (PSS) proportions for PSS and PSS were 76-80% and 68-81%, respectively. Furthermore, the thermal half-lives () of compounds A2-A4 and B2 ranged from 0.9 to 5.3 h, affected by the diverse substituents at the R and R positions. The results indicated that azo photoswitches based on the phenolylazoindole scaffold had stationary photophysical properties and wouldn't be excessively affected by modifying the functional groups. Compounds A4 and B2, which were modified with an aryl group, also exhibited fluorescence emission properties (the quantum yields of A4 and B2 were 2.32% and 13.34%) through the modification of the flexible conjugated structure (benzene) at the R position. Significantly, compound C1 was obtained modification with a pharmacophore in order to acquire antifungal activities against three plant fungi, (), (), and (). Strikingly, the inhibitory activity of the -isomer of compound C1towards (53.3%) was significantly better than that of the -isomer (34.2%) at 50 μg mL. In order to further reveal the antifungal mechanism, molecular docking simulations demonstrated that compound C1 effectively integrates into the cavity of succinate dehydrogenase (SDH); the optically controlled -isomer showed a lower binding energy with SDH than that of the -isomer. This research confirmed that phenolylazoindole photoswitches can be appropriately applied as molecular regulatory devices and functional photoswitch molecules bis-functionalization.