Abstract
Ion-molecule reactions of diethylsilylium ions with hexamethyldisilazane and isobutylamine were studied radiochemically. These reactions, like the previously studied reactions of diethylsilylium ions with tert-butylaminotrimethylsilane, occur exclusively along the condensation pathway; in both cases, the diethylsilylium ion undergoes a rearrangement. The extremely low degree of rearrangement of the diethylsilylium ion and high yield of the labeled substrate in the reaction with isobutylamine are due to the presence of two labile N-H hydrogen atoms, resulting in active isotope exchange between the Si-T tritium atoms and N-H hydrogen atoms and in shorter lifetime of the condensation complex, caused by more intense bimolecular deprotonation of the complex.
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Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 9, 2005, pp. 1471–1473.
Original Russian Text Copyright © 2005 by Vrazhnov, Kochina, Sinotova, Ignat'ev, Kalinin.
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Vrazhnov, D.V., Kochina, T.A., Sinotova, E.N. et al. Radiochemical Study of the Reactions of Diethylsilylium Ions with Hexamethyldisilazane and Isobutylamine in the Gas Phase. Russ J Gen Chem 75, 1399–1401 (2005). https://doi.org/10.1007/s11176-005-0436-2
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DOI: https://doi.org/10.1007/s11176-005-0436-2