Hydrocarbon activation by “bare” uranium cations: formation of a cationic uranium-benzene complex from three ethylene units
Identifieur interne : 002968 ( Main/Exploration ); précédent : 002967; suivant : 002969Hydrocarbon activation by “bare” uranium cations: formation of a cationic uranium-benzene complex from three ethylene units
Auteurs : Christoph Heinemann [Allemagne] ; Hans H. Cornehl [Allemagne] ; Helmut Schwarz [Allemagne]Source :
- Journal of Organometallic Chemistry [ 0022-328X ] ; 1995.
Abstract
The ability of the atomic uranium cation U+ to activate a variety of saturated and unsaturated hydrocarbon molecules is investigated. Both CH and CC bond activation processes proceeds at markedly higher kinetic efficiencies compared with the lower congener Nd+ from the lanthanide series. Formation of a cationic uranium-benzene complex occurs in three consecutive dehydrogenation reactions between U+ and ethylene. The mechanism of this metal-mediated cyclotrimerization is enlightened by kinetic measurements, collision-induced dissociation experiments and ion-molecule reactions of the intermediate species.
Url:
DOI: 10.1016/0022-328X(95)05644-5
Affiliations:
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<front><div type="abstract" xml:lang="en">The ability of the atomic uranium cation U+ to activate a variety of saturated and unsaturated hydrocarbon molecules is investigated. Both CH and CC bond activation processes proceeds at markedly higher kinetic efficiencies compared with the lower congener Nd+ from the lanthanide series. Formation of a cationic uranium-benzene complex occurs in three consecutive dehydrogenation reactions between U+ and ethylene. The mechanism of this metal-mediated cyclotrimerization is enlightened by kinetic measurements, collision-induced dissociation experiments and ion-molecule reactions of the intermediate species.</div>
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