Corentin Rossi, Giel Muller, Nicolas Solem, Roland Thissen, Claire Romanzin, Christian Alcaraz, Jean-Christophe Loison and Ugo Jacovella*,
{"title":"Possible Hydrocarbon Chemical Growth Routes from l-C3H+ in Dense Molecular Clouds","authors":"Corentin Rossi, Giel Muller, Nicolas Solem, Roland Thissen, Claire Romanzin, Christian Alcaraz, Jean-Christophe Loison and Ugo Jacovella*, ","doi":"10.1021/acsearthspacechem.4c0032310.1021/acsearthspacechem.4c00323","DOIUrl":null,"url":null,"abstract":"<p >The C<sub>3</sub>H<sup>+</sup> cation plays a pivotal role within the chemical network of dense interstellar clouds. Its relatively slow reaction with molecular hydrogen (H<sub>2</sub>) suggests that reactions with other species, particularly small hydrocarbons, may play a significant role. In this study, we measured the absolute reaction cross sections of C<sub>3</sub>H<sup>+</sup> with acetylene (C<sub>2</sub>H<sub>2</sub>) and the two isomers of C<sub>3</sub>H<sub>4</sub> (allene and propyne). To facilitate the implementation of our experimental data into astrochemical models, we converted the reaction cross sections into rate constants. No temperature dependency was observed for all of the investigated channels. The reaction rates for C<sub>3</sub>H<sup>+</sup> with C<sub>2</sub>H<sub>2</sub> and C<sub>3</sub>H<sub>4</sub>, yielding C<sub>5</sub>H<sub>2</sub><sup>+</sup> and C<sub>4</sub>H<sub>3</sub><sup>+</sup>, respectively, are in good agreement with existing data. However, we report a previously unidentified channel in the reaction with C<sub>3</sub>H<sub>4</sub>, leading to protonated acetylene C<sub>2</sub>H<sub>3</sub><sup>+</sup> with a 30% yield compared to the major product, C<sub>4</sub>H<sub>3</sub><sup>+</sup>.</p>","PeriodicalId":15,"journal":{"name":"ACS Earth and Space Chemistry","volume":"9 2","pages":"349–355 349–355"},"PeriodicalIF":2.9000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Earth and Space Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsearthspacechem.4c00323","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The C3H+ cation plays a pivotal role within the chemical network of dense interstellar clouds. Its relatively slow reaction with molecular hydrogen (H2) suggests that reactions with other species, particularly small hydrocarbons, may play a significant role. In this study, we measured the absolute reaction cross sections of C3H+ with acetylene (C2H2) and the two isomers of C3H4 (allene and propyne). To facilitate the implementation of our experimental data into astrochemical models, we converted the reaction cross sections into rate constants. No temperature dependency was observed for all of the investigated channels. The reaction rates for C3H+ with C2H2 and C3H4, yielding C5H2+ and C4H3+, respectively, are in good agreement with existing data. However, we report a previously unidentified channel in the reaction with C3H4, leading to protonated acetylene C2H3+ with a 30% yield compared to the major product, C4H3+.
期刊介绍:
The scope of ACS Earth and Space Chemistry includes the application of analytical, experimental and theoretical chemistry to investigate research questions relevant to the Earth and Space. The journal encompasses the highly interdisciplinary nature of research in this area, while emphasizing chemistry and chemical research tools as the unifying theme. The journal publishes broadly in the domains of high- and low-temperature geochemistry, atmospheric chemistry, marine chemistry, planetary chemistry, astrochemistry, and analytical geochemistry. ACS Earth and Space Chemistry publishes Articles, Letters, Reviews, and Features to provide flexible formats to readily communicate all aspects of research in these fields.