Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Details

Autor(en) / Beteiligte
Titel
Interstellar Detection of O-protonated Carbonyl Sulfide, HOCS
Ist Teil von
  • The Astrophysical journal, 2024-04, Vol.965 (2), p.149
Ort / Verlag
Philadelphia: IOP Publishing
Erscheinungsjahr
2024
Link zum Volltext
Quelle
EZB*
Beschreibungen/Notizen
  • We present the first detection in space of O-protonated carbonyl sulfide (HOCS+), in the midst of an ultradeep molecular line survey toward the G+0.693-0.027 molecular cloud. From the observation of all Ka = 0 transitions ranging from Jlo = 2 to Jlo = 13 of HOCS+ covered by our survey, we derive a column density of N = (9 ± 2) × 1012 cm−2, translating into a fractional abundance relative to H2 of ∼7 × 10−11. Conversely, the S-protonated HSCO+ isomer remains undetected, and we derive an upper limit to its abundance with respect to H2 of ≤3 × 10−11, a factor of ≥2.3 less abundant than HOCS+. We obtain an HOCS+/OCS ratio of ∼2.5 × 10−3, in good agreement with the prediction of astrochemical models. These models show that one of the main chemical routes to the interstellar formation of HOCS+ is likely the protonation of OCS, which appears to be more efficient at the oxygen end. Also, we find that high values of cosmic-ray ionization rates (10−15–10−14 s−1) are needed to reproduce the observed abundance of HOCS+. In addition, we compare the O/S ratio across different interstellar environments. G+0.693-0.027 appears as the source with the lowest O/S ratio. We find an HOCO+/HOCS+ ratio of ∼31, in accordance with other O/S molecular pairs detected toward this region and also close to the O/S solar value (∼37). This fact indicates that S is not significantly depleted within this cloud due to the action of large-scale shocks, unlike in other sources where S-bearing species remain trapped on icy dust grains.
Sprache
Englisch
Identifikatoren
ISSN: 0004-637X
eISSN: 1538-4357
DOI: 10.3847/1538-4357/ad2c01
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_8751ab5c029847029934eda247a7ba9e

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX