Electronic excitation of C4F6 isomers by ...
Document type :
Article dans une revue scientifique: Article original
Title :
Electronic excitation of C4F6 isomers by electron impact
Author(s) :
Anzai, K. [Auteur]
Kato, H. [Auteur]
Hoshino, M. [Auteur]
The University of Tokyo [UTokyo]
Mogi, D. [Auteur]
Tanioka, T. [Auteur]
Duflot, D. [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Limão-Vieira, P. [Auteur]
Tanaka, H. [Auteur]
Kato, H. [Auteur]
Hoshino, M. [Auteur]
The University of Tokyo [UTokyo]
Mogi, D. [Auteur]
Tanioka, T. [Auteur]
Duflot, D. [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Limão-Vieira, P. [Auteur]
Tanaka, H. [Auteur]
Journal title :
Journal of Physics: Conference Series
Pages :
2050
Publisher :
IOP Science
Publication date :
2012-11
ISSN :
1742-6588
HAL domain(s) :
Physique [physics]/Physique [physics]/Chimie-Physique [physics.chem-ph]
English abstract : [en]
We have measured electronic excitation differential cross sections for C4F6 molecules isomers by electron impact. In the case of hexafluoro-1,3-butadiene we observed an optical forbidden transition at around 5 eV. The ...
Show more >We have measured electronic excitation differential cross sections for C4F6 molecules isomers by electron impact. In the case of hexafluoro-1,3-butadiene we observed an optical forbidden transition at around 5 eV. The spectra of the three C4F6 isomers show the most intense band clearly shifted to lower energies when going from 2-C4F6, to c-C4F6 and to 1,3-C4F6.Show less >
Show more >We have measured electronic excitation differential cross sections for C4F6 molecules isomers by electron impact. In the case of hexafluoro-1,3-butadiene we observed an optical forbidden transition at around 5 eV. The spectra of the three C4F6 isomers show the most intense band clearly shifted to lower energies when going from 2-C4F6, to c-C4F6 and to 1,3-C4F6.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Source :
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