arXiv subjects

J. Cernicharo

Publications and source records attributed to J. Cernicharo.

At least 73 records · Page 4Linked to original sources

arXiv2021

Discovery of two isomers of ethynyl cyclopentadiene in TMC-1: Abundances of CCH and CN derivatives of hydrocarbon cycles

We report the detection of two isomers of ethynyl cyclopentadiene (c-C5H5CCH), namely 1- and 2-ethynyl-1,3-cyclopentadiene, in the direction of TMC-1. We derive column densities of (1.4 +/- 0.2)e12 cm-2, and (2.0 +/- 0.4)e12 cm-2, respectively, for these two cyclopentadiene derivatives, which imply that they are about ten times less abundant than cyclopentadiene. We also report the tentative detection of ethynyl benzene (C6H5CCH), for which we estimate a column density of (2.5 +/-0.4)e12 cm-2. We derived abundances for the corresponding cyano derivatives of cyclopentadiene and benzene and found values significantly lower than previously reported. The rotational temperature of the ethynyl and cyano derivatives of these cycles is about 9 K, that is, very close to the gas kinetic temperature of the cloud. The abundance ratio of the 1- and 2- isomers of ethynyl cyclopentadiene is 1.4 +/-0.5, while for the two isomers of cyano cyclopentadiene it is 2.4 +/- 0.6. The relative abundances of CCH over CN derivatives is 7.7 +/- 2.2 for cyclopentadiene, which probably reflects the abundance ratio of the radicals CCH and CN; this ratio is only 2.1 +/- 0.5 for benzene, which suggests that additional reactions besides cyano radicals with benzene are involved in the formation of benzonitrile. The formation of these cycles is reasonably well accounted for through a chemical scheme based on neutral-neutral reactions. It is predicted that benzene should be as abundant as cyclopentadiene in TMC-1.

astro-ph.GA↗

arXiv2021

Discovery of benzyne, o-C6H4, in TMC-1 with the QUIJOTE line survey

We report the detection, for the first time in space, of a new non-functionalised hydrocarbon cycle in the direction of TMC-1: o-C6H4 (ortho-benzyne). We derive a column density for this hydrocarbon cycle of (5 +/- 1)e11 cm-2. The abundance of this species is around 30 times lower than that of cyclopentadiene and indene. We compare the abundance of benzyne with that of other pure hydrocarbons, cycles or chains, and find that it could be formed from neutral-radical reactions such as C2H + CH2CHCCH and C + C5H5, and possibly through C4H + C2H4, C3H + CH2CCH2, and C3H2 + C3H3. Hence, the rich content of hydrocarbon cycles observed in TMC-1 could arise through a bottom-up scenario involving reactions of a few radicals with the abundant hydrocarbons recently revealed by the QUIJOTE line survey.

astro-ph.GA↗

arXiv2021

Magnesium radicals MgC$_5$N and MgC$_6$H in IRC+10216

After the previous discovery of MgC$_3$N and MgC$_4$H in IRC+10216, a deeper Q-band (31.0-50.3 GHz) integration on this source had revealed two additional series of harmonically related doublets that we assigned on the basis of quantum mechanical calculations to the larger radicals MgC$_5$N and MgC$_6$H. The results presented here extend and confirm previous results on magnesium-bearing molecules in IRC\,+10216. We derived column densities of (4.7$\pm$1.3)$\times$10$^{12}$ for MgC$_5$N and (2.0$\pm$0.9)$\times$10$^{13}$ for MgC$_6$H, which imply that MgC$_5$N/MgC$_3$N=0.5 and MgC$_6$H/MgC$_4$H = 0.9. Therefore, MgC$_5$N and MgC$_6$H are present with column densities not so different from those of the immediately shorter analogs. The synthesis of these large magnesium cyanides and acetylides in IRC+10216 can be explained for their shorter counterparts by a two-step process initiated by the radiative association of Mg$^+$ with large cyanopolyynes and polyynes, which are still quite abundant in this source, followed by the dissociative recombination of the ionic complexes.

astro-ph.GA↗

arXiv2021

Interstellar detection of the simplest aminocarbyne, H2NC: an ignored but abundant molecule

We report the first identification in space of H2NC, a high-energy isomer of H2CN that has been largely ignored in chemical and astrochemical studies. The observation of various unidentified lines around 72.2 GHz in the cold dark cloud L483 motivated the search for, and successful detection of, additional groups of lines in harmonic relation. After an exhaustive high-level ab initio screening of possible carriers, we confidently assign the unidentified lines to H2NC based on the good agreement between astronomical and theoretical spectroscopic parameters and sound spectroscopic and astrochemical arguments. The observed frequencies are used to precisely characterize the rotational spectrum of H2NC. This species is also detected in the cold dark cloud B1-b and the z=0.89 galaxy in front of the quasar PKS1830-211. We derive H2NC/H2CN abundance ratios of 1 in L483 and B1-b and 0.27 toward PKS1830-211. Neither H2NC nor H2CN are detected in the dark cloud TMC-1, which seriously questions a previous identification of H2CN in this source. We suggest that the H2NC/H2CN ratio behaves as the HNC/HCN ratio, with values close to one in cold dense clouds and below one in diffuse clouds. The reactions N + CH3 and C + NH3 emerge as strong candidates to produce H2NC in interstellar clouds. Further studies on these two reactions are needed to evaluate the yield of H2NC. Due to the small number of atoms involved, it should be feasible to constrain the chemistry behind H2NC and H2CN, just as it has been done for HNC and HCN, as this could allow to use the H2NC/H2CN ratio as a probe of chemical or physical conditions of the host clouds.

astro-ph.GA↗

arXiv2021

Detection of deuterated methylcyanoacetylene, CH$_2$DC$_3$N, in TMC-1

We report the first detection in space of the single deuterated isotopologue of methylcyanoacetylene, CH$_2$DC$_3$N. A total of fifteen rotational transitions, with $J$ = 8-12 and $K_a$ = 0 and 1, were identified for this species in TMC-1 in the 31.0-50.4 GHz range using the Yebes 40m radio telescope. The observed frequencies were used to derive for the first time the spectroscopic parameters of this deuterated isotopologue. We derive a column density of $(8.0\pm 0.4) \times 10^{10}$ cm$^{-2}$. The abundance ratio between CH$_3$C$_3$N and CH$_2$DC$_3$N is $\sim$22. We also theoretically computed the principal spectroscopic constants of $^{13}$C isotopologues of CH$_3$C$_3$N and CH$_3$C$_4$H and those of the deuterated isotopologues of CH$_3$C$_4$H for which we could expect a similar degree of deuteration enhancement. However, we have not detected either CH$_2$DC$_4$H nor CH$_3$C$_4$D nor any $^{13}$C isotopologue. The different observed deuterium ratios in TMC-1 are reasonably accounted for by a gas phase chemical model where the low temperature conditions favor deuteron transfer through reactions with H$_2$D$^+$.

astro-ph.GA↗

arXiv2021

Cumulene carbenes in TMC-1: Astronomical discovery of $l$-H$_2$C$_5$

We report the first detection in space of the cumulene carbon chain $l$-H$_2$C$_5$. A total of eleven rotational transitions, with $J_{up}$ = 7-10 and $K_a$ = 0 and 1, were detected in TMC-1 in the 31.0-50.4 GHz range using the Yebes 40m radio telescope. We derive a column density of (1.8$\pm$0.5)$\times$10$^{10}$ cm$^{-2}$. In addition, we report observations of other cumulene carbenes detected previously in TMC-1, to compare their abundances with the newly detected cumulene carbene chain. We find that $l$-H$_2$C$_5$ is $\sim$4.0 times less abundant than the larger cumulene carbene $l$-H$_2$C$_6$, while it is $\sim$300 and $\sim$500 times less abundant than the shorter chains $l$-H$_2$C$_3$ and $l$-H$_2$C$_4$. We discuss the most likely gas-phase chemical routes to these cumulenes in TMC-1 and stress that chemical kinetics studies able to distinguish between different isomers are needed to shed light on the chemistry of C$_n$H$_2$ isomers with $n$\,$>$\,3.

astro-ph.GA↗

arXiv2021

The sulphur saga in TMC-1: Discovery of HCSCN and HCSCCH

We report the detection, for the first time in space, of cyano thioformaldehyde (HCSCN) and propynethial (HCSCCH) towards the starless core TMC-1. Cyano thioformaldehyde presents a series of prominent a- and b-type lines, which are the strongest previously unassigned features in our Q-band line survey of TMC-1. Remarkably, HCSCN is four times more abundant than cyano formaldehyde (HCOCN). On the other hand, HCSCCH is five times less abundant than propynal (HCOCCH). Surprisingly, we find an abundance ratio HCSCCH/HCSCN of 0.25, in contrast with most other ethynyl-cyanide pairs of molecules for which the CCH-bearing species is more abundant than the CN-bearing one. We discuss the formation of these molecules in terms of neutral-neutral reactions of S atoms with CH2CCH and CH2CN radicals as well as of CCH and CN radicals with H2CS. The calculated abundances for the sulphur-bearing species are, however, significantly below the observed values, which points to an underestimation of the abundance of atomic sulphur in the model or to missing formation reactions, such as ion-neutral reactions.

astro-ph.GA↗

arXiv2021

Multi-frequency high spectral resolution observations of HCN toward the circumstellar envelope of Y CVn

High spectral resolution observations toward the low mass-loss rate C-rich, J-type AGB star Y CVn have been carried out at 7.5, 13.1 and 14.0 um with SOFIA/EXES and IRTF/TEXES. Around 130 HCN and H13CN lines of bands v2, 2v2, 2v2-v2, 3v2-2v2, 3v2-v2, and 4v2-2v2 have been identified involving lower levels with energies up to ~3900 K. These lines have been complemented with the pure rotational lines J=1-0 and 3-2 of the vibrational states up to 2v2 acquired with the IRAM 30 m telescope, and with the continuum taken with ISO. We have analyzed the data with a ro-vibrational diagram and a code which models the absorption and emission of the circumstellar envelope of an AGB star. The continuum is produced by the star with a small contribution from dust grains comprising warm to hot SiC and cold amorphous carbon. The HCN abundance distribution seems to be anisotropic. The ejected gas is accelerated up to the terminal velocity (~8 km/s) from the photosphere to ~3R* but there is evidence of higher velocities (>9-10 km/s) beyond this region. In the vicinity of Y CVn, the line widths are as high as ~10 km/s, which implies a maximum turbulent velocity of 6 km/s or the existence of other physical mechanisms probably related to matter ejection that involve higher gas expansion velocities than expected. HCN is rotationally and vibrationally out of LTE throughout the whole envelope. A difference of about 1500 K in the rotational temperature at the photosphere is needed to explain the observations at 7.5 and 13-14 um. Our analysis finds a total HCN column density that ranges from ~2.1E+18 to 3.5E+18 cm^{-2}, an abundance with respect to H2 of 3.5E-05 to 1.3E-04, and a 12C/13C isotopic ratio of ~2.5 throughout the whole envelope.

astro-ph.SR↗

arXiv2021

Pure hydrocarbon cycles in TMC-1: Discovery of ethynyl cyclopropenylidene, cyclopentadiene and indene

We report the detection for the first time in space of three new pure hydrocarbon cycles in TMC-1: c-C3HCCH (ethynyl cyclopropenylidene), c-C5H6 (cyclopentadiene) and c-C9H8 (indene). We derive a column density of 3.1e11 cm-2 for the former cycle and similar values, in the range (1-2)e13 cm-2, for the two latter molecules. 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-C3H2. The high abundance found for these two hydrocarbon cycles, together with the high abundance previously found for the propargyl radical (CH2CCH) and other hydrocarbons like vinyl and allenyl acetylene (Agundez et al. 2021; Cernicharo et al. 2021a,b), 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-C3HCCH is most likely formed through the reaction between the radical CCH and c-C3H2, the high observed abundances of cyclopentadiene and indene are difficult to explain through currently proposed chemical mechanisms. Further studies are needed to identify how are five- and six-membered rings formed under the cold conditions of clouds like TMC-1.

astro-ph.GA↗

arXiv2021

O-bearing complex organic molecules at the cyanopolyyne peak of TMC-1: detection of C2H3CHO, C2H3OH, HCOOCH3, and CH3OCH3

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)e11 cm-2, (2.5 +/- 0.5)e12 cm-2, (1.1 +/- 0.2)e12 cm-2, and (2.5 +/- 0.7)e12 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.

astro-ph.GA↗

arXiv2021

First detection of doubly deuterated methyl acetylene (CHD2CCH and CH2DCCD)

We report the first detection in space of the two doubly deuterated isotopologues of methyl acetylene. The species CHD2CCH and CH2DCCD were identified in the dense core L483 through nine and eight, respectively, rotational lines in the 72-116 GHz range using the IRAM 30m telescope. The astronomical frequencies observed here were combined with laboratory frequencies from the literature measured in the 29-47 GHz range to derive more accurate spectroscopic parameters for the two isotopologues. We derive beam-averaged column densities of (2.7 +/- 0.5)e12 cm-2 for CHD2CCH and (2.2 +/- 0.4)e12 cm-2 for CH2DCCD, which translate to abundance ratios CH3CCH/CHD2CCH = 34 +/- 10 and CH3CCH/CH2DCCD = 42 +/- 13. The doubly deuterated isotopologues of methyl acetylene are only a few times less abundant than the singly deuterated ones, concretely around 2.4 times less abundant than CH3CCD. The abundances of the different deuterated isotopologues with respect to CH3CCH are reasonably accounted for by a gas-phase chemical model in which deuteration occurs from the precursor ions C3H6D+ and C3H5D+, when the ortho-to-para ratio of molecular hydrogen is sufficiently low. This points to gas-phase chemical reactions, rather than grain-surface processes, as responsible for the formation and deuterium fractionation of CH3CCH in L483. The abundance ratios CH2DCCH/CH3CCD = 3.0 +/- 0.9 and CHD2CCH/CH2DCCD = 1.25 +/- 0.37 observed in L483 are consistent with the statistically expected values of three and one, respectively, with the slight overabundance of CHD2CCH compared to CH2DCCD being well explained by the chemical model.

astro-ph.GA↗

arXiv2021

Submillimeter imaging of the Galactic Center starburst Sgr B2. Warm molecular, atomic, and ionized gas far from massive star-forming cores

We present 168 arcmin^2 spectral images of the Sgr B2 complex taken with Herschel/SPIRE-FTS. We detect ubiquitous emission from CO (up to J=12-11), H2O, [CI]492, 809 GHz, and [NII] 205 um lines. We also present maps of the SiO, N2H+, HCN, and HCO+ emission obtained with the IRAM30m telescope. The cloud environment dominates the emitted FIR (80%), H2O 752 GHz (60 %) mid-J CO (91%), and [CI] (93 %) luminosity. The region shows very extended [NII] emission (spatially correlated with the 24 and 70 um dust emission). The observed FIR luminosities imply G_0~10^3. The extended [CI] emission arises from a pervasive component of neutral gas with n_H~10^3 cm-3. The high ionization rates, produced by enhanced cosmic-ray (CR) fluxes, drive the gas heating to Tk~40-60 K. The mid-J CO emission arises from a similarly extended but more pressurized gas component (P_th~10^7 K cm-3). Specific regions of enhanced SiO emission and high CO-to-FIR intensity ratios (>10^-3) show mid-J CO emission compatible with shock models. A major difference compared to more quiescent star-forming clouds in the disk of our Galaxy is the extended nature of the SiO and N2H+ emission in Sgr B2. This can be explained by the presence of cloud-scale shocks, induced by cloud-cloud collisions and stellar feedback, and the much higher CR ionization rate (>10^-15 s-1) leading to overabundant H3+ and N2H+. Hence, Sgr B2 hosts a more extreme environment than star-forming regions in the disk of the Galaxy. As a usual template for extragalactic comparisons, Sgr B2 shows more similarities to ultra luminous infrared galaxies such as Arp 220, including a "deficit" in the [CI]/FIR and [NII]/FIR intensity ratios, than to pure starburst galaxies such as M82. However, it is the extended cloud environment, rather than the cores, that serves as a useful template when telescopes do not resolve such extended regions in galaxies.

astro-ph.GA↗

arXiv2021

TMC-1, the starless core sulfur factory: Discovery of NCS, HCCS, H2CCS, H2CCCS, and C4S and detection of C5S

We report the detection of the sulfur-bearing species NCS, HCCS, H2CCS, H2CCCS, and C4S for the first time in space. These molecules were found towards TMC-1 through the observation of several lines for each species. We also report the detection of C5S for the first time in a cold cloud through the observation of five lines in the 31-50 GHz range. The derived column densities are N(NCS) = (7.8 +/- 0.6)e11 cm-2, N(HCCS) = (6.8 +/- 0.6)e11 cm-2, N(H2CCS) = (7.8 +/- 0.8)e11 cm-2, N(H2CCCS) = (3.7 +/- 0.4)e11 cm-2, N(C4S) = (3.8 +/- 0.4)e10 cm-2, and N(C5S) = (5.0 +/- 1.0)e10 cm-2. The observed abundance ratio between C3S and C4S is 340, that is to say a factor of approximately one hundred larger than the corresponding value for CCS and C3S. The observational results are compared with a state-of-the-art chemical model, which is only partially successful in reproducing the observed abundances. These detections underline the need to improve chemical networks dealing with S-bearing species.

astro-ph.GA↗

arXiv2021

Discovery of the propargyl radical (CH2CCH) in TMC-1: one of the most abundant radicals ever found and a key species for cyclization to benzene in cold dark clouds

We present the first identification in interstellar space of the propargyl radical (CH2CCH). This species was observed in the cold dark cloud TMC-1 using the Yebes 40m telescope. The six strongest hyperfine components of the 2,0,2-1,0,1 rotational transition, lying at 37.46~GHz, were detected with signal-to-noise ratios in the range 4.6-12.3 sigma. We derive a column density of 8.7e13 cm-2 for CH2CCH, which translates to a fractional abundance relative to H2 of 8.7e-9. This radical has a similar abundance to methyl acetylene, with an abundance ratio CH2CCH/CH3CCH 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 CH2CCH with neutral atoms. According to the chemical model, the propargyl radical is essentially formed by the C + C2H4 reaction and by the dissociative recombination of C3Hn+ ions with n = 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.

astro-ph.GA↗

arXiv2021

Discovery of allenyl acetylene, H2CCCHCCH, in TMC-1. A study of the isomers of C5H4

We present the discovery in TMC-1 of allenyl acetylene, H2CCCHCCH, through the observation of nineteen lines with a signal-to-noise ratio ~4-15. For this species, we derived a rotational temperature of 7 +/- 1 K and a column density of (1.2 +/- 0.2)e13 cm-2. The other well known isomer of this molecule, methyl diacetylene (CH3C4H), has also been observed and we derived a similar rotational temperature, Trot = 7.0 +/- 0.3 K, and a column density for its two states (A and E) of (6.5 +/- 0.3)e12 cm-2. Hence, allenyl acetylene and methyl diacetylene have a similar abundance. Remarkably, their abundances are close to that of vinyl acetylene (CH2CHCCH). We also searched for the other isomer of C5H4, HCCCH2CCH (1.4-pentadiyne), but only a 3sigma upper limit of 2.5e12 cm-2 to the column density can be established. These results have been compared to state-of-the-art chemical models for TMC-1, indicating the important role of these hydrocarbons in its chemistry. The rotational parameters of allenyl acetylene have been improved by fitting the existing laboratory data together with the frequencies of the transitions observed in TMC-1.

astro-ph.GA↗

arXiv2021

Discovery of CH2CHCCH and detection of HCCN, HC4N, CH3CH2CN, and, tentatively, CH3CH2CCH in TMC-1

We present the discovery in TMC-1 of vinyl acetylene, CH2CHCCH, and the detection, for the first time in a cold dark cloud, of HCCN, HC4N, and CH3CH2CN. A tentative detection of CH3CH2CCH is also reported. The column density of vinyl acetylene is (1.2 +/- 0.2)e13 cm-2, which makes it one of the most abundant closed-shell hydrocarbons detected in TMC-1. Its abundance is only three times lower than that of propylene, CH3CHCH2. The column densities derived for HCCN and HC4N are (4.4 +/- 0.4)e11 cm-2 and (3.7 +/- 0.4)e11 cm-2, respectively. Hence, the HCCN/HC4N abundance ratio is 1.2 +/- 0.3. For ethyl cyanide we derive a column density of (1.1 +/- 0.3)e11 cm-2. These results are compared with a state-of-the-art chemical model of TMC-1, which is able to account for the observed abundances of these molecules through gas-phase chemical routes.

astro-ph.GA↗

arXiv2021

SiO, 29SiO, and 30SiO emission from 67 oxygen-rich stars. A survey of 61 maser lines from 7 to 1 mm

Circumstellar environments of oxygen-rich stars are among the strongest SiO maser emitters. Physical processes such as collisions, infrared pumping and overlaps favors the inversion of level population and produce maser emission at different vibrational states. Despite numerous observational and theoretical efforts, we still do not have an unified picture including all the physical processes involved in the SiO maser emission. The aim of this work is to provide homogeneous data in a large sample of oxygen-rich stars. We present a survey of 67 oxygen-rich stars from 7 to 1 mm, in their rotational transitions from J=1-0 to J=5-4, for vibrational numbers v from 0 to 6 in the three main SiO isotopologues. We have used one of the 34 m NASA antennas at Robledo and the IRAM 30 m radio telescope. The first tentative detection of a v=6 line is reported, as well as the detection of new maser lines. The highest vibrational levels seem confined to small volumes, presumably close to the stars. The J=1-0, v=2 line flux is greater than the corresponding v=1 in almost half of the sample, which may confirm a predicted dependence on the pulsation cycle. This database is potentially useful in models which should consider most of the physical agents, time dependency, and mass-loss rates. As by-product, we report detections of 27 thermal rotational lines from other molecules, including isotopologues of SiS, H2S, SO, SO2, and NaCl.

astro-ph.SR↗

arXiv2021

A study of C4H3N isomers in TMC-1: line by line detection of HCCCH2CN

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)e12 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.

astro-ph.GA↗