Theoretical Analysis of the Methane Elimination from Oxonium Cations [R3O]+, R = H, CH3-Reference-Cited by-同舟云学术

Theoretical Analysis of the Methane Elimination from Oxonium Cations [R3O]+, R = H, CH3

Published:1996-01-01 Issue:6 Volume:100 Page:2089-2093
ISSN:0022-3654
Container-title:The Journal of Physical Chemistry
language:en
Short-container-title:J. Phys. Chem.

Author:

Nguyen Minh Tho¹,Bouchoux Guy¹

Affiliation:

1. Department of Chemistry, University of Leuven, Celestijnenlaan 200F, 3001 Leuven, Belgium, and Département de Chimie, Laboratoire des Mécanismes Réactionnels CNRS/URA 1307, Ecole Polytechnique, 91128 Palaiseau Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry,General Engineering

Link

https://pubs.acs.org/doi/pdf/10.1021/jp952453%2B

Reference19 articles.

1. Concerning the heats of formation of the [C, H3, N]+ radical cations

2. Gaseous [H2, C, N]+ and [H3, C, N]+.cntdot. ions. Generation, heat of formation, and dissociation characteristics of methylenenitrenium(1+) ([H2CN]+), iminomethylene(1+) ([HCNH]+), aminomethylidene(1+) ([CNH2]+), formaldimine(1+.cntdot.) ([H2CNH]+.cntdot.), and aminomethylene(1+.cntdot.) ([HCNH2]+.cntdot.) ions

3. Fragmentation of the trimethyloxonium cation and of protonated dimethylether studied in a tandem quadrupole mass spectrometer at medium pressure

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