Abstract:Reversible color development induced by near UV light (photochromism) was observed for some crystalline powder of 1,1′-diaryl-4,4′-bipyridinium bis(p-toluenesulfonate). Redox mechanism by the electron transfer from the sulfonate anion to viologen dication is claimed.
A pyridinium-carboxylate compound undergoes reversible color change under pressure owing to the formation of radicals via electron transfer; dehydration and hydration can also trigger electron transfer.
A pyridinium-carboxylate compound undergoes reversible color change under pressure owing to the formation of radicals via electron transfer; dehydration and hydration can also trigger electron transfer.
The light‐driven reduction of protons for the production of molecular hydrogen in multicomponent systems depends on electron relays such as viologens. We describe here the effect of viologens appended with guest moieties (adamantane or bile acid) on the efficiency of a system composed of a cyclodextrin‐appended photosensitizer [Ir(ppy)2(pytl‐βCD)]Cl [ppy = 2‐phenylpyridine; pytl = 2‐(1‐substituted‐1H‐1,2,3‐triazol‐4‐yl)pyridine; CD = cyclodextrin], cyclodextrin‐modified Pt nanoparticles as the catalyst, and ethylenediaminetetraacetic acid (EDTA) as the sacrificial donor. The system was designed to self‐assemble in a supramolecular manner in order to promote electron transfer and produce hydrogen. Cyclic voltammetry (CV) measurements in DMF showed that the electron‐donating adamantyl substituent decreases the reduction potential of the viologen. The use of symmetric and asymmetric guest‐appended viologens gave rise to unexpected phenomena in the H2 evolution. The presence of adamantane or bile acid groups on the viologen induced stabilization and aggregation of the radical cations in water, which is disadvantageous for hydrogen formation.
“…After the online publication of this Communication (March 30, 2007), it has been brought to the authors' attention that the 13 C NMR spectra of the assumed azepinoazepine synthesized are essentially identical to those of the viologen structure 1 . 1 H NMR spectra also support this finding, although they were measured in different solvents and at different field strengths 2. The authors therefore retract this Communication and apologize for any inconvenience.…”
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