Predictive Guidelines for Electrocyclization of Dithienylethenes.

Molecular photoswitches undergo a structural transformation upon photoexcitation to interconvert between two or more stable forms. In some cases, the structural rearrangement involves the transition between ring-open and ring-closed forms. In this work, we develop simple guidelines for the design of organic molecules able to undergo photochemical electrocyclization, using electronic structure calculations on dithienylethene (DTE)-based compounds. We conclude that the ability to photocyclize can be predicted from the localization and symmetry of frontier molecular orbitals. These ideas are based on the Woodward-Hoffmann rules but go beyond them, allowing us to address a more general family of chromophores. Our methodology has been experimentally validated in a novel series of quinoline-based DTEs, where the ability for photocyclization depends on specific chemical modifications. We use the DTE scaffold as the workhorse model in our study; however, these simple yet powerful guidelines are expected to be generally valid to guide the design of other diarylethenes.