Article ID Journal Published Year Pages File Type
10575209 Journal of Organometallic Chemistry 2005 7 Pages PDF
Abstract
(all-E)-2,5-Bis[2-[1′-[2-(1′,2,2′,3,3′,4,4′,5-octamethylferrocenyl)ethenyl]ruthenocenyl]ethenyl]thiophene was synthesized by Wittig olefinations. The X-ray structure of the intermediate (E)-2-(1′-formylruthenocenyl)ethenyl-1′,2,2′,3,3′,4,4′,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
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