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A chiral photoswitchable nanoporous material with remote-controllable enantioselective adsorption capacity is presented. This metal–organic framework possesses both homochiral D-camphoric acid and light-responsive azobenzene moieties. Although the structure at the chiral moieties is unaffected, the transcis-azobenzene-photoisomerization changes the pore environment and, thus, switches the enantioselective adsorption behavior of the homochiral MOF.

Graphical abstract: Switching the enantioselectivity of nanoporous host materials by light

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