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Article Dans Une Revue International Journal of Mass Spectrometry Année : 2002

Thermochemistry and unimolecular reactivity of protonated alpha,omega-aminoalcohols in the gas phase

Résumé

Competitive deamination and dehydration of protonated alpha,omega-antmoalcohols (1,2-aminoethanol (1), 1,3-aminopropanol (2), 1,4-aminobutanol (3) and 1,5-aminopentanol (4)) in the gas-phase has been examined by both tandem mass spectrometry experiments including metastable ions decompositions and collisional activation (CA) techniques and molecular orbital calculations. For all the precursor molecules 1-4, CA experiments demonstrate that the low energy product ions are either a protonated cyclic amine or a protonated cyclic ether. The mechanisms of the internal nucleophilic substitution reactions leading to these products have been detailed at the MP2/6-31G* level of theory. The thermochemistry associated with the initial protonation process of 1-4 has been examined up to the G2(MP2,SVP) level. (C) 2002 Elsevier Science B.V All rights reserved.

Dates et versions

hal-00918610 , version 1 (23-12-2013)

Identifiants

Citer

Guy Bouchoux, Nadège Choret, Florence Berruyer-Penaud, R. Flammang. Thermochemistry and unimolecular reactivity of protonated alpha,omega-aminoalcohols in the gas phase. International Journal of Mass Spectrometry, 2002, 217 (1), pp.195-230. ⟨10.1016/S1387-3806(02)00577-8⟩. ⟨hal-00918610⟩
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