C. Cabezas, M. Ag'undez, Y. Endo, B. Tercero, N. Marcelino, P. D. Vicente, J. Cernicharo
{"title":"Discovery of the interstellar cyanoacetylene radical cation HC_3N+","authors":"C. Cabezas, M. Ag'undez, Y. Endo, B. Tercero, N. Marcelino, P. D. Vicente, J. Cernicharo","doi":"10.1051/0004-6361/202451081","DOIUrl":null,"url":null,"abstract":"We report the first identification in space of HC$_3$N$^+$, the simplest member of the family\nof cyanopolyyne cations. Three rotational transitions with half-integer quantum numbers from $J$=7/2 to\n11/2 have been observed with the Yebes 40m radio telescope and assigned to HC$_3$N$^+$, which has an inverted\n$^2 ground electronic state. The three rotational transitions exhibit several hyperfine components due to the magnetic and nuclear quadrupole coupling effects of the H and N nuclei. We confidently assign the characteristic rotational spectrum pattern to HC$_3$N$^+$ based on the good agreement between the astronomical and theoretical spectroscopic parameters. We derived a column density of (6.0pm 0.6)times 1010 $ and a rotational temperature of 4.5pm 1\\,K. The abundance ratio between HC$_3$N and HC$_3$N$^+$ is 3200pm 320. As found for the larger members of the family of cyanopolyyne cations (HC$_5$N$^+$ and HC$_7$N$^+$), HC$_3$N$^+$ is mainly formed through the reactions of H$_2$ and the cation C$_3$N$^+$ and by the reactions of H$^+$ with HC$_3$N. In the same manner than other cyanopolyyne cations, HC$_3$N$^+$ is mostly destroyed through a reaction with H$_2$ and a dissociative recombination with electrons.","PeriodicalId":505693,"journal":{"name":"Astronomy & Astrophysics","volume":"68 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Astronomy & Astrophysics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1051/0004-6361/202451081","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We report the first identification in space of HC$_3$N$^+$, the simplest member of the family
of cyanopolyyne cations. Three rotational transitions with half-integer quantum numbers from $J$=7/2 to
11/2 have been observed with the Yebes 40m radio telescope and assigned to HC$_3$N$^+$, which has an inverted
$^2 ground electronic state. The three rotational transitions exhibit several hyperfine components due to the magnetic and nuclear quadrupole coupling effects of the H and N nuclei. We confidently assign the characteristic rotational spectrum pattern to HC$_3$N$^+$ based on the good agreement between the astronomical and theoretical spectroscopic parameters. We derived a column density of (6.0pm 0.6)times 1010 $ and a rotational temperature of 4.5pm 1\,K. The abundance ratio between HC$_3$N and HC$_3$N$^+$ is 3200pm 320. As found for the larger members of the family of cyanopolyyne cations (HC$_5$N$^+$ and HC$_7$N$^+$), HC$_3$N$^+$ is mainly formed through the reactions of H$_2$ and the cation C$_3$N$^+$ and by the reactions of H$^+$ with HC$_3$N. In the same manner than other cyanopolyyne cations, HC$_3$N$^+$ is mostly destroyed through a reaction with H$_2$ and a dissociative recombination with electrons.