Enantiodivergent epoxidation of alkenes with a photoswitchable phosphate manganese-salen complex

The development of enantiodivergent catalysts capable of preparing both enantiomeric products from one substrate in a controlled fashion is challenging. Introducing a switching function into the catalyst can address this challenge, allowing the chiral reaction environment to reversibly change during catalysis. Here we report a photoswitchable phosphate ligand, derived from 2,2 '-biphenol, which axially coordinates as the counterion to an achiral manganese(III)-salen catalyst, providing the latter with the ability to switch stereoselectivity in the epoxidation of alkenes. The enantiomers of the chiral ligand exist as a pair of pseudo-enantiomers, which can be interconverted by irradiation with light of different wavelengths. The opposite axial chirality of these pseudo-enantiomers is efficiently transferred to the manganese(III)-salen catalyst. With this switchable supramolecular catalyst, the enantioselectivity of the epoxidation of a variety of alkenes can be controlled, resulting in opposite enantiomeric excesses of the epoxide products. This transfer of chirality from a photoswitchable anionic ligand to a metal complex broadens the scope of supramolecular catalysts. Developing enantiodivergent catalysts capable of preparing both enantiomeric products from one substrate in a controlled fashion is challenging. Now, a manganese(III)-salen complex with a chiral photoswitchable phosphate counterion is reported for the epoxidation of alkenes in a stereoselective manner, where irradiation with light allows access to either enantiomer of the epoxide.