Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10575209 | Journal of Organometallic Chemistry | 2005 | 7 Pages |
Abstract
(all-E)-2,5-Bis[2-[1â²-[2-(1â²,2,2â²,3,3â²,4,4â²,5-octamethylferrocenyl)ethenyl]ruthenocenyl]ethenyl]thiophene was synthesized by Wittig olefinations. The X-ray structure of the intermediate (E)-2-(1â²-formylruthenocenyl)ethenyl-1â²,2,2â²,3,3â²,4,4â²,5-octamethylferrocene is reported. The cyclic voltammogram of this quatermetallocene exhibits completely unusual redox properties. In contrast to most ruthenocene-containing compounds, a reversible two-electron transfer is observed at a significantly lower potential than found usually for ruthenocenes that can be attributed unambiguously to the independent oxidation/reduction of the two ruthenocene moieties.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Dagmar Obendorf, Herwig Schottenberger, Klaus Wurst, Norbert Schuler, Gerhard Laus,