We report the detection of the oxygen-bearing complex organic molecules propenal (C2H3CHO), vinyl alcohol (C2H3OH), methyl formate (HCOOCH3), and dimethyl ether (CH3OCH3) toward the cyanopolyyne peak ...of the starless core TMC-1. These molecules are detected through several emission lines in a deep Q-band line survey of TMC-1 carried out with the Yebes 40m telescope. These observations reveal that the cyanopolyyne peak of TMC-1, which is the prototype of cold dark cloud rich in carbon chains, contains also O-bearing complex organic molecules like HCOOCH3 and CH3OCH3, which have been previously seen in a handful of cold interstellar clouds. In addition, this is the first secure detection of C2H3OH in space and the first time that C2H3CHO and C2H3OH are detected in a cold environment, adding new pieces in the puzzle of complex organic molecules in cold sources. We derive column densities of (2.2 ± 0.3) × 1011 cm™2, (2.5 ± 0.5) × 1012 cm-2, (1.1 ± 0.2) × 1012 cm-2, and (2.5 ± 0.7) × 1012 cm-2 for C2H3CHO, C2H3OH, HCOOCH3, and CH3OCH3, respectively. Interestingly, C2H3OH has an abundance similar to that of its well known isomer acetaldehyde (CH3CHO), with C2H3OH/CH3CHO ~ 1 at the cyanopolyyne peak. We discuss potential formation routes to these molecules and recognize that further experimental, theoretical, and astronomical studies are needed to elucidate the true mechanism of formation of these O-bearing complex organic molecules in cold interstellar sources.
We report the detection for the first time in space of three new pure hydrocarbon cycles in TMC-1:
c
-C
3
HCCH (ethynyl cyclopropenylidene),
c
-C
5
H
6
(cyclopentadiene), and
c
-C
9
H
8
(indene). We ...derive a column density of 3.1 × 10
11
cm
−2
for the first cycle and similar values, in the range (1−2) × 10
13
cm
−2
, for the second and third. This means that cyclopentadiene and indene, in spite of their large size, are exceptionally abundant, only a factor of five less abundant than the ubiquitous cyclic hydrocarbon
c
-C
3
H
2
. The high abundance found for these two hydrocarbon cycles together with the high abundance previously found for the propargyl radical (CH
2
CCH) and other hydrocarbons, such as vinyl and allenyl acetylene (Agúndez et al. 2021, A&A, 647, L10; Cernicharo et al. 2021a, A&A, 647, L2; Cernicharo et al. 2021b, A&A, 647, L3), start to allow us to quantify the abundant content of hydrocarbon rings in cold dark clouds and to identify the intermediate species that are probably behind the in situ bottom-up synthesis of aromatic cycles in these environments. While
c
-C
3
HCCH is most likely formed through the reaction between the radical CCH and
c
-C
3
H
2
, the high observed abundances of cyclopentadiene and indene are difficult to explain through currently proposed chemical mechanisms. Further studies are needed to identify how five- and six-membered rings are formed under the cold conditions of a cloud such as TMC-1.
We present the first identification in interstellar space of the thioformyl radical (HCS) and its metastable isomer HSC. These species were detected toward the molecular cloud L483 through ...observations carried out with the IRAM 30 m telescope in the λ3 mm band. We derive beam-averaged column densities of 7 × 1012 cm−2 for HCS and 1.8 × 1011 cm−2 for HSC, which translate into fractional abundances relative to H2 of 2 × 10−10 and 6 × 10−12, respectively. Although the amount of sulfur locked by these radicals is low, their detection allows placing interesting constraints on the chemistry of sulfur in dark clouds. Interestingly, the H2CS/HCS abundance ratio is found to be quite low, ~1, in contrast with the oxygen analog case, in which the H2CO/HCO abundance ratio is around 10 in dark clouds. Moreover, the radical HCS is found to be more abundant than its oxygen analog, HCO. The metastable species HOC, the oxygen analog of HSC, has not yet been observed in space. These observational constraints are compared with the outcome of a recent model of the chemistry of sulfur in dark clouds. The model underestimates the fractional abundance of HCS by at least one order of magnitude, overestimates the H2CS/HCS abundance ratio, and does not provide an abundance prediction for the metastable isomer HSC. These observations should prompt a revision of the chemistry of sulfur in interstellar clouds.
We present Yebes 40m telescope observations of the three most stable C4H3N isomers towards the cyanopolyyne peak of TMC-1. We have detected 13 transitions from CH3C3N (A and E species), 16 lines from ...CH2CCHCN, and 27 lines (a-type and b-type) from HCCCH2CN. We thus provide a robust confirmation of the detection of HCCCH2CN and CH2CCHCN in space. We have constructed rotational diagrams for the three species, and obtained rotational temperatures between 4-8 K and similar column densities for the three isomers, in the range (1.5-3)×1012 cm-2. Our chemical model provides abundances of the order of the observed ones, although it overestimates the abundance of CH3CCCN and underestimates that of HCCCH2CN. The similarity of the observed abundances of the three isomers suggests a common origin, most probably involving reactions of the radical CN with the unsaturated hydrocarbons methyl acetylene and allene. Studies of reaction kinetics at low temperature and further observations of these molecules in different astronomical sources are needed to draw a clear picture of the chemistry of C4H3N isomers in space.
An exhaustive chemical characterization of dense cores is mandatory to our understanding of chemical composition changes from a starless to a protostellar stage. However, only a few sources have had ...their molecular composition characterized in detail. Here we present a
3 mm line survey of L483, a dense core around a Class 0 protostar, which was observed with the IRAM 30m telescope in the 80-116 GHz frequency range. We detected 71 molecules (140 including different isotopologs), most of which are present in the cold and quiescent ambient cloud according to their narrow lines (FWHM ~0.5 km s
) and low rotational temperatures (≲10 K). Of particular interest among the detected molecules are the
isomer of HCOOH, the complex organic molecules HCOOCH
, CH
OCH
, and C
H
OH, a wide variety of carbon chains, nitrogen oxides like N
O, and saturated molecules like CH
SH, in addition to eight new interstellar molecules (HCCO, HCS, HSC, NCCNH
, CNCN, NCO, H
NCO
, and NS
) whose detection has already been reported. In general, fractional molecular abundances in L483 are systematically lower than in TMC-1 (especially for carbon chains), tend to be higher than in L1544 and B1-b, and are similar to those in L1527. Apart from the overabundance of carbon chains in TMC-1, we find that L483 does not have a marked chemical differentiation with respect to starless/prestellar cores like TMC-1 and L1544, although it does chemically differentiate from Class 0 hot corino sources like IRAS 16293-2422. This fact suggests that the chemical composition of the ambient cloud of some Class 0 sources could be largely inherited from the dark cloud starless/prestellar phase. We explore the use of potential chemical evolutionary indicators, such as the HNCO/C
S, SO
/C
S, and CH
SH/C
S ratios, to trace the prestellar/protostellar transition. We also derived isotopic ratios for a variety of molecules, many of which show isotopic ratios close to the values for the local interstellar medium (remarkably all those involving
S and
S), while there are also several isotopic anomalies like an extreme depletion in
C for one of the two isotopologs of
-C
H
, a drastic enrichment in
O for SO and HNCO (SO being also largely enriched in
O), and different abundances for the two
C substituted species of C
H and the two
N substituted species of N
H
. We report the first detection in space of some minor isotopologs like
-C
D. The exhaustive chemical characterization of L483 presented here, together with similar studies of other prestellar and protostellar sources, should allow us to identify the main factors that regulate the chemical composition of cores along the process of formation of low-mass protostars.
Our observations of TMC-1 with the Yebes 40 m radio telescope in the 31.0–50.3 GHz range allowed us to detect a group of unidentified lines, showing a complex line pattern indicative of an open-shell ...species. The observed frequencies of these lines and the similarity of the spectral pattern with that of the 2
0, 2
–1
0, 1
rotational transition of H
2
CCN indicate that the lines arise from the deuterated cyanomethyl radical, HDCCN. Using Fourier transform microwave spectroscopy experiments combined with electric discharges, we succeeded in producing the radical HDCCN in the laboratory and observed its 1
0, 1
–0
0, 0
and 2
0, 2
–1
0, 1
rotational transitions. From our observations and assuming a rotational temperature of 5 K, we derive an abundance ratio H
2
CCN/HDCCN = 20 ± 4. The high abundance of the deuterated form of H
2
CCN is well accounted for by a standard gas-phase model, in which deuteration is driven by deuteron transfer from the H
2
D
+
molecular ion.
It is thought that dicyanopolyynes could be potentially abundant interstellar molecules, although their lack of dipole moment makes it impossible to detect them through radioastronomical techniques. ...Recently, the simplest member of this chemical family, cyanogen (NCCN), was indirectly probed for the first time in interstellar space through the detection of its protonated form toward the dense clouds L483 and TMC-1. Here we present a second firm evidence of the presence of NCCN in interstellar space, namely the detection of the metastable and polar isomer isocyanogen (CNCN). This species has been identified in L483 and tentatively in TMC-1 by observing various rotational transitions in the λ 3 mm band with the IRAM 30m telescope. We derive beam-averaged column densities for CNCN of 1.6 × 10
cm
in L483 and 9 × 10
cm
in TMC-1, which imply fractional abundances relative to H
in the range (5 - 9) × 10
. While the presence of NCCN in interstellar clouds seems out of doubt owing to the detection of NCCNH
and CNCN, putting tight constraints on its abundance is still hampered by the poor knowledge of the chemistry that links NCCN with NCCNH
and especially with CNCN. We estimate that NCCN could be fairly abundant, in the range 10
-10
relative to H
, as other abundant nitriles like HCN and HC
N.
We present a study of the isocyano isomers of the cyanopolyynes HC3N, HC5N, and HC7N in TMC-1 and IRC+10216 carried out with the Yebes 40m radio telescope. This study has enabled us to report the ...detection, for the first time in space, of HCCCCNC in TMC-1 and to give upper limits for HC6NC in the same source. In addition, the deuterated isotopologues of HCCNC and HNCCC were detected, along with all 13C substitutions of HCCNC, also for the first time in space. The abundance ratios of HC3N and HC5N, with their isomers, are very different in TMC-1 and IRC+10216, namely, N(HC5N)/N(HC4NC) is ~300 and ≥2100, respectively. We discuss the chemistry of the metastable isomers of cyanopolyynes in terms of the most likely formation pathways and by comparing observational abundance ratios between different sources.
We present the first identification in interstellar space of the propargyl radical (CH
CCH). This species was observed in the cold dark cloud TMC-1 using the Yebes 40m telescope. The six strongest ...hyperfine components of the 2
-1
rotational transition, lying at 37.46 GHz, were detected with signal-to-noise ratios in the range 4.6-12.3 σ. We derive a column density of 8.7 × 10
cm
for CH
CCH, which translates to a fractional abundance relative to H
of 8.7 × 10
. This radical has a similar abundance to methyl acetylene, with an abundance ratio CH
CCH/CH
CCH close to one. The propargyl radical is thus one of the most abundant radicals detected in TMC-1, and it is probably the most abundant organic radical with a certain chemical complexity ever found in a cold dark cloud. We constructed a gas-phase chemical model and find calculated abundances that agree with, or fall two orders of magnitude below, the observed value depending on the poorly constrained low-temperature reactivity of CH
CCH with neutral atoms. According to the chemical model, the propargyl radical is essentially formed by the C + C
H
reaction and by the dissociative recombination of C
H
ions with
= 4-6. The propargyl radical is believed to control the synthesis of the first aromatic ring in combustion processes, and it probably plays a key role in the synthesis of large organic molecules and cyclization processes to benzene in cold dark clouds.
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