Journal of Organometallic Chemistry p. 303 - 311 (1991)
Update date:2022-08-16
Topics:
Pertici, Paolo
Barretta, Gloria Uccello
Burzagli, Fabrizio
Salvadori, Piero
Bennett, Martin A.
1,5-Cyclooctadiene and 1-hexene undergo isomerization to 1,3-cyclooctadiene and (E)-/(Z)-2-hexene, respectively, with high turnover number in the presence of the complex Ru(η6-naphthalene)(η4-1,5-cyclooctadiene) and acetonitrile.This high catalytic activity is observed only using acetonitrile as co-catalyst.A possible reaction mechanism, based on results from an 1H and 2H NMR study of the isomerization, is presented.
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