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Table 1
Molecular lines of interest covered by the SMA observations.
Transitions | Rest frequency | Eup | Transitions | Rest frequency | Eup |
---|---|---|---|---|---|
(GHz) | (K) | (GHz) | (K) | ||
(RxA lower sideband) | (RxB lower sideband) | ||||
C34S 5–4 | 241.016 | 27.8 | CH3OH vt = 1 5−1,5-4−1,4 E | 241.203 | 326.2 |
CS 5–4 | 244.935 | 35.3 | CH3OH vt = 1 52,4-42,3 A | 241.192 | 333.4 |
(RxA upper sideband) | CH3OH vt = 1 52,3-42,2 A | 241.196 | 333.4 | ||
CH3CCH 120–110 | 205.081 | 64.0 | CH3OH vt = 1 50,5–40,4 E | 241.206 | 333.5 |
CH3CCH 121–111 | 205.076 | 71.1 | CH3OH vt = 1 53,3–43,2 E | 241.180 | 357.4 |
CH3CCH 122–112 | 205.065 | 92.5 | CH3OH vt = 1 5−3,2–4−3,1 E | 241.180 | 357.4 |
CH3CCH 123–113 | 205.045 | 128.2 | CH3CN 130–120 | 239.138 | 80.3 |
CH3CCH 124–114 | 205.018 | 178.2 | CH3CN 131–121 | 239.133 | 87.5 |
H2CS 60,6–50,5 | 205.987 | 34.6 | CH3CN 132–122 | 239.119 | 108.9 |
H2CS 62,5–52,4 | 206.054 | 87.3 | CH3CN 133–123 | 239.096 | 144.6 |
H2CS 62,4–52,3 | 206.159 | 87.3 | CH3CN 134–124 | 239.064 | 194.6 |
H2CS 63,4–53,3 | 206.053 | 153.1 | CH3CN 135–125 | 239.023 | 258.9 |
H2CS 63,3–53,2 | 206.053 | 153.1 | CH3CCH 140–130 | 239.252 | 82.1 |
H2CS 64,3–54,2 | 206.002 | 245.1 | CH3CCH 141–131 | 239.248 | 93.3 |
H2CS 64,2–54,1 | 206.002 | 245.1 | CH3CCH 142–132 | 239.234 | 114.7 |
SO 45–34 | 206.176 | 38.6 | CH3CCH 143–133 | 239.211 | 150.3 |
SO2 32,2–21,1 | 208.700 | 15.3 | CH3CCH 144–134 | 239.179 | 200.3 |
(RxB lower sideband) | H2CS 70,7–60,6 | 240.267 | 46.1 | ||
CH3OH 50,5–40,4 A | 241.791 | 34.8 | H2CS 72,6–62,5 | 240.382 | 98.8 |
CH3OH 51,5–41,4 E | 241.767 | 40.4 | H2CS 73,5–63,4 | 240.392 | 164.6 |
CH3OH 50,5–40,4 E | 241.700 | 47.9 | H2CS 73,4–63,3 | 240.393 | 164.6 |
CH3OH 5−1,4–4−1,3 E | 241.879 | 55.9 | H2CS 74,4–64,3 | 240.332 | 256.5 |
CH3OH 5−2,4–4−2,3 E | 241.905 | 57.1 | H2CS 74,3–64,2 | 240.332 | 256.5 |
CH3OH 52,3–42,3 E | 241.904 | 60.7 | SO2 140,14–131,13 | 244.254 | 93.9 |
CH3OH 52,4–42,3 A | 241.842 | 72.5 | (RxB upper sideband) | ||
CH3OH 52,3–42,2 A | 241.887 | 72.5 | C2H N = 3–2, J = 7∕2–5/2, F = 3–2 | 262.01 | 25.1 |
CH3OH 5−3,3–4−3,2 E | 241.844 | 82.5 | C2H N = 3–2, J = 7∕2–5/2, F = 4–3 | 262.00 | 25.1 |
CH3OH 53,3–43,2 A | 241.833 | 84.7 | C2H N = 3–2, J = 5∕2–3/2, F = 3–2 | 262.06 | 25.1 |
CH3OH 53,2–43,1 A | 241.833 | 84.7 | C2H N = 3–2, J = 5∕2–3/2, F = 2–2 | 262.08 | 25.2 |
CH3OH 53,3 –43,2 E | 241.852 | 97.5 | C2H N = 3–2, J = 5∕2–3/2, F = 2–1 | 262.07 | 25.2 |
CH3OH 53,3 –43,2 A | 241.807 | 115.2 | CH3CCH 150–140 | 256.337 | 98.4 |
CH3OH 54,1 –44,0 A | 241.807 | 115.2 | CH3CCH 151–141 | 256.331 | 105.6 |
CH3OH 54,2 –44,1 E | 241.813 | 122.7 | CH3CCH 152–142 | 256.317 | 127.0 |
CH3OH 5−4,1 –4−4,0 E | 241.830 | 130.8 | CH3CCH 153–143 | 256.292 | 162.7 |
CH3CCH 154–144 | 256.258 | 212.6 | |||
H13CO+ 3–2 | 260.255 | 25.0 | |||
SO 66 –55 | 258.256 | 56.5 | |||
SO 76 –65 | 261.843 | 47.6 |
Notes. The information is from the CDMS database (Müller et al. 2001).
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