Acetylene; Dissociation; Electroionization; Photoionization; Coincidence; Kinetic energy
Abstract :
[en] The dissociative ionization of C2H2, C2D2 and C2HD is presented in this work. Excepting the H2+ formation, all dissociation channels are thoroughly investigated by electron impact. The translational energy distribution as a function of the impinging electron energy and the appearance energy as a function of the translational energy are measured for all fragment ions. KE versus AE diagrams are obtained and the isotope effect is examined. All observed thresholds are analyzed in detail and dissociation mechanisms are proposed. For the C2H+ ion the PIPECO technique has also been used. From these discussions the H-C2H, HC-CH and H-C2 binding energy values are proposed, i.e. 5.33+/-0.23 eV, 9.83+/0.10 eV and 5.44+/-0.40 eV respectively. The fragmentation path leading to C+, CH2+ and C2+ are discussed in terms of dissociation mechanisms involving the transient vinylidene structure of the molecular ion as an intermediate.
Research Center/Unit :
Laboratoire de Dynamique Moléculaire
Disciplines :
Chemistry
Author, co-author :
Locht, Robert ; Université de Liège - ULiège > Département de Chimie (Faculté des sciences) > Laboratoire de Dynamique Moléculaire (Sciences)
Servais, Christian ; Université de Liège - ULiège > Département d'astrophys., géophysique et océanographie (AGO) > Groupe infra-rouge de phys. atmosph. et solaire (GIRPAS)
Language :
English
Title :
How complex can be the Unimolecular Decomposition of a simple Molecule? The case of Acetylene. An Electron Impact and PIPECO Investigation.
Alternative titles :
[fr] Quelle est la complexité de la décomposition unimoléculaire d'une molécule simple? Le cas de l'Acétylene. Une étude par impact électronique et par PIPECO.
Publication date :
1996
Journal title :
Zeitschrift für Physikalische Chemie
ISSN :
0942-9352
eISSN :
2196-7156
Publisher :
Oldenburg Verlag, München, Germany
Special issue title :
Dedicated to Prof. Baumgärtel
Volume :
195
Pages :
153-179
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
F.R.S.-FNRS - Fonds de la Recherche Scientifique FRFC - Fonds de la Recherche Fondamentale Collective
Commentary :
- PDF-version of Editor's Postprint available on request
- Version-pdf du tiré-à-part disponible sur demande
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