arXiv subjects

M. Agundez

Publications and source records attributed to M. Agundez.

At least 37 records · Page 2Linked to original sources

arXiv2022

Discovery of C5H+ and detection of C3H+ in TMC-1 with the QUIJOTE line survey

We report the discovery of the C5H+ cation toward TMC-1 with the QUIJOTE line survey. Four lines from J=7-6 up to J=10-9 have been identified in perfect harmonic frequency relation that can be fit with B=2411.94397 +/-0.00055 MHz and D=138+/-3 Hz. The standard deviation of the fit is 4.4 kHz. After discarding potential candidates, C5H- among them, we conclude that the carrier is C5H+, for which accurate ab initio calculations provide B=2410.3 MHz. We also report for the first time in a cold starless core the detection of the C3H+ cation. The column densities we derive for C5H+ and C3H+ are (8.8+/-0.5)e10 cm-2 and (2.4+/-0.2)e10 cm-2, respectively. Hence, the C5H+/C3H+ abundance ratio is 3.7+/-0.5. The fact that C5H+ is more abundant than C3H+ is well explained by dedicated chemical models and is due to the slow reactivity of C5H+ with H2, while C3H+ reacts with H2.

astro-ph.GA↗

arXiv2021

Discovery of the elusive thioketenylium, HCCS+, in TMC-1

We report the detection in TMC-1 of the cation HCCS+ (3Sigma-), which is the protonated form of the widespread radical CCS. This is the first time that a protonated radical has been detected in a cold dark cloud. Twenty-six hyperfine components from twelve rotational transitions have been observed with the Yebes 40m and IRAM 30m radio telescopes. We confidently assign the characteristic rotational spectrum pattern to HCCS+ based on the good agreement between the astronomical and theoretical spectroscopic parameters. The column density of HCCS+ is (1.1+/-0.1)e12 cm-2, and the CCS/HCCS+ abundance ratio is 50+/-10, which is very similar to that of CS/HCS+ (35+/-8) and CCCS/HCCCS+ (65+/-20). From a state-of-the-art gas-phase chemical model, we conclude that HCCS+ is mostly formed by reactions of proton transfer from abundant cations such as HCO+, H3O+, and H3+ to the radical CCS.

astro-ph.GA↗

arXiv2021

New deuterated species in TMC-1: Detection of CH2DC4H with the QUIJOTE line survey

We report the first detection in space of the single deuterated isotopologue of methyldiacetylene, CH2DC4H. A total of 12 rotational transitions, with J = 8-12 and Ka = 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 allowed us to obtain, for the first time, the spectroscopic parameters of this deuterated isotopologue. We derived a column density of (5.5+/-0.2)e11 cm-2. The abundance ratio between CH3C4H and CH2DC4H is 24+/-2. This ratio is similar to that found for the CH3C3N/CH2DC3N analogue system, which is 22+/-2.We did not detect the deuterated species CH3C4D, which has already been observed in laboratory experiments. The detection of deuterated CH3C4H allows us to extend the discussion on the chemical mechanisms of deuterium fractionation at work in TMC-1 using a new gas-phase chemical model with multiply deuterated molecules. Introducing a possible deuterium exchange reaction between CH3CCH and atomic deuterium allows us to account for the CH3C4H/CH2DC4H abundance ratio.

astro-ph.GA↗

arXiv2021

Detection of the propargyl radical at lambda 3 mm

We report the detection of the propargyl radical (CH2CCH) in the cold dark cloud TMC-1 in the lambda 3 mm wavelength band. We recently discovered this species in space toward the same source at a wavelength of lambda 8 mm. In those observations, various hyperfine components of the 2,0,2-1,0,1 rotational transition, at 37.5 GHz, were detected using the Yebes 40m telescope. Here, we used the IRAM 30m telescope to detect ten hyperfine components of the 5,0,5-4,0,4 rotational transition, lying at 93.6 GHz. The observed frequencies differ by 0.2 MHz with respect to the predictions from available laboratory data. This difference is significant for a radioastronomical search for CH2CCH in interstellar sources with narrow lines. We thus included the measured frequencies in a new spectroscopic analysis to provide accurate frequency predictions for the interstellar search for propargyl at mm wavelengths. Moreover, we recommend that future searches for CH2CCH in cold interstellar clouds are carried out at lambda 3 mm, rather than at lambda 8 mm. The 5,0,5-4,0,4 transition is about five times more intense than the 2,0,2-1,0,1 one in TMC-1, which implies that detecting the former requires about seven times less telescope time than detecting the latter. We constrain the rotational temperature of CH2CCH in TMC-1 to 9.9 +/- 1.5 K, which indicates that the rotational levels of this species are thermalized at the gas kinetic temperature. The revised value of the column density of CH2CCH (including ortho and para species) is (1.0 +/- 0.2)e14 cm-2, and thus the CH2CCH/CH3CCH abundance ratio is revised from slightly below one to nearly one. This study opens the door for future detections of CH2CCH in other cold interstellar clouds, making possible to further investigate the role of this very abundant hydrocarbon radical in the synthesis of large organic molecules such as aromatic rings.

astro-ph.GA↗

arXiv2021

Discovery of HCCCO and C5O in TMC-1 with the QUIJOTE line survey

We report on the detection, for the first time in space, of the radical HCCCO and of pentacarbon monoxide, C5O. The derived column densities are (1.6+/-0.2)e11 cm-2 and (1.5+/-0.2)e10 cm-2, respectively. We have also analysed the data for all the molecular species of the families HCnO and CnO within our QUIJOTE line survey. Upper limits are obtained for HC4O, HC6O, C4O, and C6O. We report a robust detection of HC5O and HC7O based on 14 and 12 rotational lines detected with a signal-to-noise ratio >30 and >5,respectively. The derived N(HC3O)/N(HC5O) abundance ratio is 0.09+/-0.03, while N(C3O)/N(C5O) is 80+/-2, and N(HC5O)/N(HC7O) is 2.2+/-0.3. As opposed to the cyanopolyyne family, HC2n+1N, which shows a continuous decrease in the abundances with increasing n, the CnO and HCnO species show a clear abundance maximum for n=3 and 5, respectively. They also show an odd and even abundance alternation, with odd values of n being the most abundant, which is reminiscent of the behaviour of CnH radicals, where in that case species with even values of n are more abundant. We explored the formation of these species through two mechanisms previously proposed, which are based on radiative associations between CnHm+ ions with CO and reactions of Cn- and CnH- anions with O atoms, and we found that several species, such as C5O, HC4O, and HC6O, are significantly overestimated. Our understanding of how these species are formed is incomplete as of yet. Other routes based on neutral-neutral reactions such as those of Cn and CnH carbon chains with O, OH, or HCO, could be behind the formation of these species.

astro-ph.GA↗

arXiv2021

Laboratory observation and astronomical search of 1-cyano propargyl radical, HCCCHCN

The reaction between carbon atoms and vinyl cyanide, CH2CHCN, is a formation route to interstellar 3-cyano propargyl radical, CH2C3N, a species that has recently been discovered in space. The 1-cyano propargyl radical (HC3HCN), an isomer of CH2C3N, is predicted to be produced in the same reaction at least twice more effciently than CH2C3N. Hence, HC3HCN is a plausible candidate to be observed in space as well. We aim to generate the HC3HCN radical in the gas phase in order to investigate its rotational spectrum. The derived spectroscopic parameters for this species will be used to obtain reliable frequency predictions to support its detection in space.The HC3HCN radical was produced by an electric discharge, and its rotational spectrum was characterized using a Balle-Flygare narrowband-type Fourier-transform microwave spectrometer operating in the frequency region of 4-40 GHz. The spectral analysis was supported by high-level ab initio calculations. A total of 193 hyperfine components that originated from 12 rotational transitions, a- and b-type, were measured for the HC3HCN radical. The analysis allowed us to accurately determine 22 molecular constants, including rotational and centrifugal distortion constants as well as the fine and hyperfine constants. Transition frequency predictions were used to search for the HC3HCN radical in TMC-1 using the QUIJOTE survey between 30.1-50.4 GHz. We do not detect HC3HCN in TMC-1 and derive a 3sigma upper limit to its column density of 6.0e11 cm-2.

astro-ph.GA↗

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.

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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

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

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

Structure and dynamics of the inner nebula around the symbiotic stellar system R Aqr

We investigate the structure, dynamics, and chemistry of the molecule-rich nebula around the stellar symbiotic system R Aqr, which is significantly affected by the presence of a white dwarf (WD) companion. We study the effects of the strong dynamical interaction between the AGB wind and the WD and of photodissociation by the WD UV radiation on the circumstellar shells. We obtained high-quality ALMA maps of the 12CO J=2-1, J=3-2, and J=6-5 lines and of 13CO J=3-2. The maps were analyzed by means of a heuristic 3D model that is able to reproduce the observations. In order to interpret this description of the molecule-rich nebula, we performed sophisticated calculations of hydrodynamical interaction and photoinduced chemistry. We find that the CO-emitting gas is distributed within a relatively small region <~ 1.5". Its structure consists of a central dense component plus strongly disrupted outer regions, which seem to be parts of spiral arms that are highly focused on the orbital plane. The structure and dynamics of these spiral arms are compatible with our hydrodynamical calculations. We argue that the observed nebula is the result of the dynamical interaction between the wind and the gravitational attraction of the WD. We also find that UV emission from the hot companion efficiently photodissociates molecules except in the densest and best-shielded regions, that is, in the close surroundings of the AGB star and some shreds of the spiral arms from which the detected lines come. We can offer a faithful description of the distribution of nebular gas in this prototypical source, which will be a useful template for studying material around other tight binary systems.

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

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

Quantum study of reaction O(3P) + H2(v,j) $\rightarrow$ OH + H: OH formation in strongly UV-irradiated gas

The reaction between atomic oxygen and molecular hydrogen is an important one in astrochemistry as it regulates the abundance of the hydroxyl radical and serves to open the chemistry of oxygen in diverse astronomical environments. However, the existence of a high activation barrier in the reaction with ground state oxygen atoms limits its efficiency in cold gas. In this study we calculate the dependence of the reaction rate coefficient on the rotational and vibrational state of H$_2$ and evaluate the impact on the abundance of OH in interstellar regions strongly irradiated by far-UV photons, where H2 can be efficiently pumped to excited vibrational states. We use a recently calculated potential energy surface and carry out time-independent quantum mechanical scattering calculations to compute rate coefficients for the reaction O(3P) + H2(v,j) -> OH + H, with H2 in vibrational states v = 0-7 and rotational states j = 0-10. We find that the reaction becomes significantly faster with increasing vibrational quantum number of H2, although even for high vibrational states of H2 (v = 4-5) for which the reaction is barrierless, the rate coefficient does not strictly attain the collision limit and still maintains a positive dependence with temperature. We implemented the calculated state-specific rate coefficients in the Meudon PDR code to model the Orion Bar PDR and evaluate the impact on the abundance of the OH radical. We find the fractional abundance of OH is enhanced by up to one order of magnitude in regions of the cloud corresponding to Av = 1.3-2.3, compared to the use of a thermal rate coefficient for O + H2, although the impact on the column density of OH is modest, of about 60 %. The calculated rate coefficients will be useful to model and interpret JWST observations of OH in strongly UV-illuminated environments.

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↗