A photo-switchable molecular capsule: sequential photoinduced processes

The metastable trilacunary heteropolyoxomolybdate [PMo 9 O 31 (py) 3 ] 3− - {PMo 9 } ; py = pyridine) and the ditopic pyridyl bearing diarylethene (DAE) (C 25 H 16 N 2 F 6 S 2 ) self-assemble via a facile ligand replacement methodology to yield the photo-active molecular capsule [(PMo 9 O 31 ) 2 (DAE) 3 ] 6− . The spatial arrangement and conformation of the three DAE ligands are directed by the surface chemistry of the molecular metal oxide precursor with exclusive ligation of the photo-active antiparallel rotamer to the polyoxometalate (POM) while the integrity of the assembly in solution has been verified by a suite of spectroscopic techniques. Electrocyclisation of the three DAEs occurs sequentially and has been investigated using a combination of steady-state and time-resolved spectroscopies with the discovery of a photochemical cascade whereby rapid photoinduced ring closure is followed by electron transfer from the ring-closed DAE to the POM in the latent donor-acceptor system on subsequent excitation. This interpretation is also supported by computational and detailed spectroelectrochemical analysis. Ring-closing quantum yields were also determined using a custom quantum yield determination setup (QYDS), providing insight into the impact of POM coordination on these processes. The metastable trilacunary heteropolyoxomolybdate [PMo 9 O 31 (py) 3 ] 3− ; py = pyridine) and the ditopic pyridyl bearing diarylethene (DAE) (C 25 H 16 N 2 F 6 S 2 ) self-assemble via a facile ligand replacement methodology to yield the photo-active molecular capsule [(PMo 9 O 31 ) 2 (DAE) 3 ] 6 − .