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Table 2

Molecular species in this work.

Molecule Transition Frequency Eup log10 Aij
(GHz) K

Single pointing
SO 55 –44 215.22065 44.10 − 3.92
DCO+ 3–2 216.11258 20.74 − 2.62
c-C3 H2 33,0 –22,1 216.27876 19.47 − 3.33
DCN 3–2 217.23863 20.85 − 4.24
c-C3 H2 a 6–5 217.82215 38.61 − 3.23
c-C3 H2 51,4 –42,3 217.94005 35.42 − 3.35
p-H2 CO 30,3 –20,2 218.22219 20.96 − 3.55
CH3 OH 42,2 –31,2 218.44005 45.45 − 4.33
p-H2 CO 32,2 –22,1 218.47563 68.09 − 3.80
p-H2 CO 32,1 –22,0 218.76007 68.11 − 3.80
C2 H 4–3 J = 9/2–7/2 F = 5–4 349.33771 41.91 − 3.88
C2 H 4–3 J = 9/2–7/2 F = 4–3 349.33899 41.91 − 3.89
C2 H 4–3 J = 7/2–5/2 F = 4–3 349.39927 41.93 − 3.90
C2 H 4–3 J = 7/2–5/2 F = 3–2 349.40067 41.93 − 3.92
o-H2 CO 51,5 –41,4 351.76864 62.45 − 2.92
DCO+ 5–4 360.16978 51.86 − 2.42
DCN 5–4 362.04575 52.12 − 3.13
HNC 4–3 362.63030 43.51 − 2.64
p-H2 CO 50,5 –40,4 362.73602 52.31 − 2.86

APEX OTF maps

13CO 4–3 440.76517 52.9 −5.27
13CO 6–5 661.06728 111.1 −4.73

JCMT and Herschel HIFI

13CO 3–2 330.58797 31.7 −5.66
13CO 10–9 1101.34960 290.8 −4.05

Notes. (a) Contains both ortho- and para forms.

References. All rest frequencies were taken from the Cologne Database for Molecular Spectroscopy (CDMS; Endres et al. 2016). The SO entry is based on Clark & De Lucia (1976). The DCO+ entries are based on Caselli & Dore (2005). The c-C3 H2 entry was based on Bogey et al. (1987) with transition frequencies important for our survey from Bogey et al. (1986) and from Spezzano et al. (2012). The DCN entries are based on Okabayashi & Tanimoto (1993) and Brünken et al. (2004). The entry for CH3 OH is based on the line list from Xu & Lovas (1997). The H2CO entries are based on experimental data from Bocquet et al. (1996). The C2 H entry is based on Padovani et al. (2009) with additional important data from Müller et al. (2000) and Sastry et al. (1981), and on Cazzoli et al. (2012), respectively. The entry for HNC is based on Okabayashi & Tanimoto (1993). The 13CO entries are based on Klapper et al. (2000).

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