New fluorescent bis-dithienylethene (DTE)-based bipyridines as reverse interrupters: single vs. double photochromismElectronic supplementary information (ESI) available. CCDC 797462. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3ob42119h

The synthesis and characterization of a series of fluorescent bis-dithienylethene (DTE)-based bipyridines, where the donor (D) and acceptor (A) groups are located on the same thiophene ring of the DTE unit, and their zinc( ii ) and rhenium( i ) complexes are reported. Their photochromic properties have been investigated by UV-visible and 1 H NMR spectroscopy. These studies reveal that in non-polar solvents it is possible to modulate the photoreactivity, single vs . double ring-closure, by changing the nature of the donor group. The solvent effect, as well as the influence of the organometallic moieties on the photochromic behavior of these molecules, is also discussed. Finally, upon photoconversion to the photostationary state (PSS), a quenching of fluorescence is observed for the bipyridine ligands, due to disruption of the conjugation upon ring-closing. The photochromic behaviour of a series of fluorescent bis-DTE-based bipyridines and their metal complexes is reported, incorporating donor and acceptor groups in the same thiophene ring.