Abstract
The syntheses of the new compounds Fe(3-Me3Si-6,6-dmch)2, 2, and Fe[3-(i-Pr)3Si-6,6-dmch]2, 3, are reported, along with X-ray structural studies of these species, and of the previously reported Fe(1,3,5,6-temch)2 (dmch = dimethylcyclohexadienyl; temch = tetramethylcyclohexadienyl). Each species crystallized in something close to the expected gauche-eclipsed conformation. In accord with previous work on Fe(6,6-dmch)2, but in contrast to results for open ferrocenes such as Fe(2,4-C7H11)2 (C7H11 = dimethylpentadienyl), the three species under study undergo reversible one-electron oxidations at room temperature to stable 17-electron cations, with potentials for oxidation being more favorable than that for ferrocene by 0.51–0.78 V. The edge-bridged open ferrocenes also react in a 1:1 ratio with TCNE (TCNE = tetracyanoethylene), yielding salts that were shown spectroscopically to contain the expected cationic 17-electron metal complexes and the TCNE radical anion.
Published Version
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