Water molecule elimination from the protonated methanol dimer ion-An example of a size-selective intracluster reaction.


Journal

The Journal of chemical physics
ISSN: 1089-7690
Titre abrégé: J Chem Phys
Pays: United States
ID NLM: 0375360

Informations de publication

Date de publication:
07 Mar 2024
Historique:
received: 04 12 2023
accepted: 12 02 2024
medline: 4 3 2024
pubmed: 4 3 2024
entrez: 4 3 2024
Statut: ppublish

Résumé

The abundance of extraterrestrial methanol makes the reaction between methanol molecules in a molecular cluster a possible key step in the search for mechanisms for the formation of more complex molecules under the conditions of the interstellar medium as well as circumstellar and planetary atmospheres. The reaction leading to the formation of the dimethyl ether ion from a methanol molecule interacting with a protonated methanol ion via the elimination of a water molecule is a basic mechanism for the formation of complex organic molecules. Here, we experimentally examine such reactions in the gas phase, analyzing the production and reactivity of protonated cluster ions formed by the ionization of a supersonic jet of methanol. Focusing especially on the post-collisional relaxation of the protonated methanol dimer and trimer ions after high-energy single collisions, the results indicate a strong size selectivity favoring the occurrence of this reaction only in the dimer ion. To elucidate this behavior, the velocity distribution of the eliminated water molecule was measured using an event-by-event coincidence analysis. These results are interpreted using quantum chemical calculations of the dissociation pathways. It turns out that in the dimer case, two transition states are able to contribute to this intracluster reaction. In the trimer case, methanol evaporation appears as the most energetically favorable relaxation pathway.

Identifiants

pubmed: 38436443
pii: 3268110
doi: 10.1063/5.0190182
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Author(s). Published under an exclusive license by AIP Publishing.

Auteurs

Thibaud Salbaing (T)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Denis Comte (D)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.
Institut für Ionenphysik und Angewandte Physik, Leopold Franzens Universität, 6020 Innsbruck, Austria.

Léo Lavy (L)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Hector Lissillour (H)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Laura Parrado Ospina (LP)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Paul Bertier (P)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Linda Feketeová (L)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Florent Calvo (F)

Université Grenoble Alpes, CNRS, LIPhy, 38000 Grenoble, France.

Bernadette Farizon (B)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Michel Farizon (M)

Université Claude Bernard Lyon 1, IP2I Lyon, UMR 5822, CNRS/IN2P3, F-69622 Villeurbanne, France.

Tilmann Märk (T)

Institut für Ionenphysik und Angewandte Physik, Leopold Franzens Universität, 6020 Innsbruck, Austria.

Classifications MeSH