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Knoezinger, H.; Corado, A.; Gati, Gy.; Hiestetter, H.; Kiss, A.; Letterer, R.; Mueller, H.D.
The symposium on the mechanisms of hydrocarbon reactions was organized by the Institute of Isotopes of the Hungarian Academy of Sciences and the Society of Hungarian Chemists at Siofok, Hungary 5-7 June 19731975
The symposium on the mechanisms of hydrocarbon reactions was organized by the Institute of Isotopes of the Hungarian Academy of Sciences and the Society of Hungarian Chemists at Siofok, Hungary 5-7 June 19731975
AbstractAbstract
[en] The isomerization and the D2-exchange of 2,3-dimethyl-1 -butene has been studied on an n-alumina which had been pre treated at only 300 deg C. Isomerization and D2-exchange reactions were both followed in a conventional microcatalytic pulse reactor, using helium or H2 as a carrier gas for the isomerization experiments and D2 for the exchange experiments. Reactant and product were separated by gas chromatography on a 2 m dimethylsulfolane/chromosorb-column at 25 deg C. The separated substances were then analyzed by NMR and mass spectroscopy. The catalysts were deuterated by exchange in D2O vapour at 300 deg C. for isomerization experiments on deuterated surfaces. The results strongly suggest an intermolecular hydrogen transfer, if the initial activity had been reduced by self-poisoning. Initially existing sites for an intramolecular hydrogen transfer are rapidly eliminated by oxygen containing residues. These observations are discussed and a proton-donor-acceptor mechanism through a cyclic, carbanion-like intermediate bound to a suitable hydrogencontainig ''active site'' is proposed. (K.A.)
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Marta, F.; Kallo, D. (eds.); p. 333-344; ISBN 9630503093;
; 1975; Akademiai Kiado; Budapest; Symposium on the mechanisms of hydrocarbon reactions; Siofok, Hungary; 5 Jun 1973; 19 refs.

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