arXiv subjects

C. Cabezas

Publications and source records attributed to C. Cabezas.

At least 19 recordsLinked to original sources

arXiv2026

Discovery of 1H-cyclopent[cd]indene (c-C11H8) in TMC-1 with the QUIJOTE line survey: A new three-ringed polycyclic aromatic hydrocarbon

We report the detection of the polycyclic aromatic hydrocarbon (PAH) 1H-cyclopent[cd]indene (c-C11H8) in TMC-1 with the QUI- JOTE line survey. We detected 22 independent lines corresponding to 88 rotational transitions with quantum numbers ranging from J=19 up to J=24 and Ka <= 5 in the Q-band range. The identification of this new PAH was based on the agreement between the rotational parameters derived from the analysis of the lines and those obtained by quantum chemical calculations. The column density derived for 1H-cyclopent[cd]indene is (6.0 +- 0.5) x 10^12 cm-2, with a rotational temperature of 9 K. Its abundance is high, as is that of the rest of the PAHs, but it is the lowest of all those detected to date in TMC-1, being 2.66 times less abundant than indene and 4.66 times less than phenalene. This result will help us to better understand the growth of five- and six-membered rings in dark clouds. Chemical models explaining their formation through the bottom-up model are still very incomplete and require further experimental and theoretical effort. Even so, the most likely formation reactions would occur between the smallest rings with small hydrocarbons; the most probable reaction for the formation of cyclopentindene is that between indene and C2H, C2H3, and/or their cation.

astro-ph.GA↗

arXiv2025

Piecing together formic acid isomerism in dark clouds. Detection of cis-formic acid in TMC-1 and astrochemical modeling

The presence of molecular isomers in interstellar environments has become a topic of growing interest within the astrochemical community. Contrary to predictions based on thermodynamic equilibrium, recent observations reveal a diverse array of high-energy isomers and conformers. One of the most iconic molecular isomers detected in space, formic acid (HCOOH, FA), has been the focus of extensive theoretical research aimed at understanding its speciation into cis and trans conformers in dark clouds and photodissociation regions. In this work, we report the detection of c-FA, the higher-energy conformer, using ultrasensitive observations of TMC-1. This detection adds to previous findings in the Barnard-5 and L483 dark clouds. The derived trans-to-cis isomer ratio in TMC-1, 17.5, closely matches those observed in other sources, suggesting that the same chemical processes are at play across these environments. To investigate this, we conducted detailed astrochemical gas-grain models tailored to formic acid isomerism to explain the observed ratios. Our models successfully reproduce the observed trans/cis ratios and indicate that the presence of cis-formic acid can be attributed to the release of c-FA from grains, followed by isomerization driven by the excess energy released during the desorption process, a process that we name as isomerization upon desorption. The models also show that the isomerization of t-FA to c-FA in the gas phase is negligible at 10 K, meaning the observed ratios are a direct consequence of the formation pathways of both isomers on the surface of dust grains. However, at higher temperatures, quantum tunneling mediated direct isomerization in the gas becomes significant, and the ratios converge toward the thermodynamic equilibrium value.

astro-ph.GA↗

arXiv2025

Analysis of the isotopologues of CS, CCS, CCCS, HCS+, HCCS+, and H2CS in TMC-1 with the QUIJOTE line survey

We performed a detailed analysis of the isotopologues with 13C, 34S, 33S, and 36S of the sulphur-bearing molecules CS, CCS, CCCS,HCS+, HCCS+, and H2CS towards TMC-1 using the QUIJOTE1. The observations were obtained with the Yebes radio telescope. Observations with the IRAM 30m of the most abundant isotopologues of these species are also presented and used to estimate volume densities and to constrain the excitation conditions. We report the first detection in space of C13C34S, CC33S, CCC33S, HC33S+, and HCC34S+. C36S is also detected for the first time in a cold object. We also complemented with maps that provide the spatial distribution of most of these species. Using the available collisional rate coefficients for each species, we modeled the observed line intensities using the large velocity gradient method for the radiative transfer. We report the most complete analysis of the column densities of the CnS family and to compare the abundance ratios of all detected isotopologues. Adopting a T_k for TMC-1 of 9K, we found that n(H2)=0.9-1.5X10^4cm-3 can explain the observed decline in intensity with increasing J. We derived the rot. constants for the C13C34S, CC33S, CCC33S, HC33S+, and HCC34S+ isotopologues from new laboratory data and complemented them with the frequencies of the observed lines. We find that all S isotopologues are consistent with solar isotopic abundance ratios. Accurate 12C/13C abundances were derived and, as previously suggested, the 13C isotopologues of CCS and CCCS show strong abundance anomalies depending on the position of the substituted carbon. Nevertheless, the 12C/13C abundance ratio is practically identical to the solar value for CS, HCS+, and H2CS. We also searched for the isotopologues of other S-bearing molecules. The expected intensities for their 34S and 13C isotopologues are too low to be detected with the present sensitivity of the QUIJOTE, however.

astro-ph.GA↗

arXiv2025

Low D/H ratio for benzonitrile in TMC-1: Implication for the origin of polycyclic aromatic hydrocarbons in cold dark clouds

Radioastronomical observations have recently discovered PAHs of moderate size (up to 24 carbon atoms) in cold dark clouds, although it is currently unknown whether they are formed in situ through a bottom-up mechanism or from larger PAHs (20-100 carbon atoms) inherited from a previous diffuse stage in a top-down scenario. Infrared observations have recently shown that large PAHs present in UV-illuminated regions are strongly enriched in deuterium. In order to shed light on the origin of PAHs in cold clouds, we have searched for deuterated benzonitrile in the cold dark cloud TMC-1. To that purpose we have synthesized the three isomers (ortho, meta, and para) of monodeuterated benzonitrile, measured their rotational spectra across the 2-18 GHz and 75-110 GHz frequency ranges in the laboratory, and searched for them in TMC-1 using data from the QUIJOTE line survey. We did not detect any of the three species and have derived a 3sigma upper limit on the column density of each of them of 3.0e10 cm-2, meaning a fractional abundance relative to H2 of <3e-12. We derived a D/H ratio (which we define as the total number of D atoms with respect to the total number of H atoms present in benzonitrile) of <1.2 %. This value is in line with the range of D/H ratios observed for other molecules in TMC-1 (0.06-3.3 %), where deuterium enrichment is explained in terms of isotopic fractionation at low temperature. It is however below the range of D/H ratios derived for large unspecific PAHs from JWST observations of the galactic PDRs Orion Bar and M17 and the galaxies M51 and NGC3256-S (between 1% and <17%). Although it is not straightforward to compare the deuteration of PAHs in dark and UV-irradiated clouds, our results suggest that the population of PAHs detected in cold dark clouds does not result from the fragmentation of larger PAHs inherited from the previous diffuse stage in a top-down scenario.

astro-ph.GA↗

arXiv2025

First detection of HS2 in a cold dark cloud

We report the first detection of HS2 towards the cold dark cloud TMC-1. This is the first observation of a chemical species containing more than one sulphur atom in this type of sources. The astronomical observations are part of QUIJOTE, a line survey of TMC-1 in the Q band (31-50 GHz). The detection is confirmed by the observation of the fine and hyperfine components of two rotational transitions (2(0,2)-1(0,1) and 3(0,3)-2(0,2)). Assuming a rotational temperature of 7 K, we derived an HS2 column density of 5.7x10^11 cm-2, using a local thermodynamic equilibrium model that reproduces the observed spectra. The abundance of HS2 relative to H2 is 5.7x10^-11, which means that it is about seven times more abundant than its oxygenated counterpart HSO. We also explored the main formation and destruction mechanisms of HS2 using a chemical model, which reproduces the observed abundance of HS2 and indicates that dissociative recombination reactions from the ions H2S2+ and H3S2+ play a major role in forming HS2.

astro-ph.GA↗

arXiv2025

A search for the three isomers of cyano-1,3-butadiene in TMC-1: Implications for bottom-up routes involving 1,3-butadiene

The molecule 1,3-butadiene (CH2CHCHCH2) could play a key role in the synthesis of the cyclic molecules cyclopentadiene and benzene in cold dense clouds. Since 1,3-butadiene is non-polar, we searched for its cyano derivative, which exists in the form of three different polar isomers, in the cold dense cloud TMC-1. We used the most recent data obtained with the Yebes 40m telescope in the Q band (31.0-50.3 GHz) in the frame of the QUIJOTE project. We do not detect any of the two isomers of 1-cyano-1,3-butadiene, and derive 3sigma upper limits to their column densities of 1.2e10 cm-2 and 2.0e10 cm-2 for E- and Z-1-cyano-1,3-butadiene, respectively. Our results are not consistent with those from Cooke et al. (2023), who determine a column density of 3.8e10 cm-2 for E-1-cyano-1,3-butadiene in TMC-1 using GBT data and a line stack technique. At the current level of sensitivity of our data, there is tentative evidence for the presence of the third cyano derivative isomer, 2-cyano-1,3-butadiene, although a firm detection must await more sensitive data. We derive an upper limit to its column density of 3.1e10 cm-2. This isomer cannot be formed in the reaction between CN and 1,3-butadiene, according to experimental and theoretical studies, and thus we speculate whether it could arise from neutral-neutral reactions like C2H3 + CH2CHCN and CH2CCN + C2H4. From the upper limit on the abundance of 1-cyano-1,3-butadiene derived here, we estimate that the abundance of 1,3-butadiene in TMC-1 is below 1e-11 - 1e-10 relative to H2. The low abundance inferred for 1,3-butadiene makes it unlikely that it plays an important role in bottom-up routes to cyclopentadiene and benzene.

astro-ph.GA↗

arXiv2025

Detection of thioacetaldehyde (CH3CHS) in TMC-1: sulfur-oxygen differentiation along the hydrogenation sequence

In recent years the chemistry of sulfur in the interstellar medium has experienced a renewed interest due to the detection of a large variety of molecules containing sulfur. Here we report the first identification in space of a new S-bearing molecule, thioacetaldehyde (CH3CHS), which is the sulfur counterpart of acetaldehyde (CH3CHO). The astronomical observations are part of QUIJOTE, a Yebes 40m Q band line survey of the cold dense cloud TMC-1. We detected seven individual lines corresponding to A and E components of the four most favorable rotational transitions of CH3CHS covered in the Q band (31.0-50.3 GHz). Assuming a rotational temperature of 9 K, we derive a column density of 9.8e10 cm-2 for CH3CHS, which implies that it is 36 times less abundant than its oxygen counterpart CH3CHO. By comparing the column densities of the O- and S-bearing molecules detected in TMC-1, we find that as molecules increase their degree of hydrogenation, sulfur-bearing molecules become less abundant compared to their oxygen analog. That is, hydrogenation seems to be less favored for S-bearing molecules than for O-bearing ones in cold sources like TMC-1. We explored potential formation pathways to CH3CHS and implemented them into a chemical model, which however underestimates by several orders of magnitude the observed abundance of thioacetaldehyde. Quantum chemical calculations carried out for one of the potential formation pathways, the S + C2H5 reaction, indicate that formation of CH3CHS is only a minor channel in this reaction.

astro-ph.GA↗

arXiv2025

Identification of the interstellar 1-cyano propargyl radical (HCCCHCN) in TMC-1

We report the first detection in interstellar medium of the 1-cyano propargyl radical, HC$_3$HCN. This species is an isomer of the 3-cyano propargyl radical (CH$_2$C$_3$N), which was recently discovered in TMC-1. The 1-cyano propargyl radical was observed in the cold dark cloud TMC-1 using data from the ongoing QUIJOTE line survey, which is being carried out with the Yebes 40m telescope. A total of seven rotational transitions with multiple hyperfine components were detected in the 31.0-50.4 GHz range. We derived a column density of (2.2$\pm$0.2)$\times$10$^{11}$ cm$^{-2}$ and a rotational temperature of 7$\pm$1\,K. The abundance ratio between HC$_3$HCN and CH$_2$C$_3$N is 1.4. The almost equal abundance of these isomers indicates that the two species may be produced in the same reaction with a similar efficiency, probably in the reaction C + CH$_2$CHCN and perhaps also in the reaction C$_2$ + CH$_3$CN and the dissociative recombination with electrons of CH$_2$C$_3$NH$^+$

astro-ph.GA↗

arXiv2024

Discovery of two cyano derivatives of acenaphthylene (C$_{12}$H$_8$) in TMC-1 with the QUIJOTE line survey

We report the discovery in TMC-1 of two cyano derivatives of the PAH acenaphthylene (C$_{12}$H$_8$). We have found two series of lines with the QUIJOTE line survey that we assign to 1-C$_{12}$H$_7$CN and 5-C$_{12}$H$_7$CN. For the 1-isomer, we have detected and assigned 173 rotational transitions with $J$ up to 46 and $K_a$ up to 9, corresponding to 107 independent frequencies. For the 5-isomer, the identification is based on 56 individual lines, corresponding to 117 rotational transitions with $J$ up to 40 and $K_a$ up to 8. Identification of the carriers was achieved through a careful analysis of the derived rotational constants, which permit us to focus on molecules larger than naphthalene but smaller than anthracene and phenanthrene. Moreover, the derived rotational constants indicate that the species are planar; this allows us to discard derivatives of fluorene and acenaphthene, which are non-planar species. Quantum chemical calculations and subsequent chemical synthesis of these molecules, as well as the observation of their rotational transitions in the laboratory, unequivocally support our identifications. We also confirm, via a robust line-by-line detection, the previous claimed detection of 1- and 2- cyanonaphthalene, which were obtained through statistical stacking techniques. The column densities of 1- and 5-cyanoacenaphthylene are (9.5\,$\pm$\,0.9)$\,\times$\,10$^{11}$ cm$^{-2}$, while those of 1- and 2-cyanonapthalene are (5.5\,$\pm$\,0.5)$\,\times$\,10$^{11}$ cm$^{-2}$. Hence, it seems that acenaphthylene could be a factor of 1.7 more abundant than naphthalene. These results support a scenario in which PAHs grow in cold dark clouds based on fused five- and six-membered carbon rings.

astro-ph.GA↗

arXiv2024

The rich interstellar reservoir of dinitriles: Detection of malononitrile and maleonitrile in TMC-1

While the nitrile group is by far the most prevalent one among interstellar molecules, the existence of interstellar dinitriles (molecules containing two -CN groups) has recently been proven. Here we report the discovery of two new dinitriles in the cold dense cloud TMC-1. These newly identified species are malononitrile, CH2(CN)2, and maleonitrile, the Z isomer of NC-CH=CH-CN, which can be seen as the result of substituting two H atoms with two -CN groups in methane and ethylene, respectively. These two molecules were detected using data from the ongoing QUIJOTE line survey of TMC-1 that is being carried out with the Yebes 40m telescope. We derive column densities of 1.8e11 cm-2 and 5.1e10 cm-2 for malononitrile and maleonitrile, respectively. This means that they are eight and three times less abundant than HCC-CH2-CN and (E)-HCC-CH=CH-CN, respectively, which are analog molecules detected in TMC-1 in which one -CN group is converted into a -CCH group. This is in line with previous findings in which -CCH derivatives are more abundant than the -CN counterparts in TMC-1. We examined the potential chemical pathways to these two dinitriles, and we find that while maleonitrile can be efficiently formed through the reaction of CN with CH2CHCN, the formation of malononitrile is not clear because the neutral-neutral reactions that could potentially form it are not feasible under the physical conditions of TMC-1.

astro-ph.GA↗

arXiv2024

More sulphur in TMC-1: Discovery of the NC$_3$S and HC$_3$S radicals with the QUIJOTE line survey

We present the detection of the free radicals NC$_3$S and HC$_3$S towards TMC-1 with the QUIJOTE line survey. The derived column densities are (1.4$\pm$0.2)$\times$10$^{11}$ for NC$_3$S and (1.5$\pm$0.2)$\times$10$^{11}$ for HC$_3$S. We searched for NCCS, but only three transitions are within the domain of our QUIJOTE line survey and the observed lines are marginally detected at the 3$σ$ level, providing an upper limit to its column density of $\leq$6$\times$10$^{10}$ cm$^{-2}$. We also unsuccessfully searched for longer species of the NC$_n$S (n$\ge$4) and HC$_n$S (n$\ge$5) families in our TMC-1 data. A chemical model based on a reduced set of reactions involving HC$_3$S and NC$_3$S predicts abundances that are 10-100 times below the observed values. These calculations indicate that the most efficient reactions of formation of HC$_3$S and NC$_3$S in the model are S + C$_3$H$_2$ and N + HC$_3$S, respectively, while both radicals are very efficiently destroyed through reactions with neutral atoms.

astro-ph.GA↗

arXiv2024

Discovery of HCCCH2CCH in TMC-1 with the QUIJOTE line survey

We present the first detection in space of 1,4-pentadiyne. It has been found towards TMC-1 with the QUIJOTE line survey in the 31-50 GHz range. We observed a total of 17 transitions with J = 2 up to 13 and Ka = 0, 1 and 2. The observed transitions allowed us to derive a rotational temperature of 9.5 +- 0.5 K and a column density of (5.0 +- 0.5) x 10^12 cm-2. This molecule was the last non-cyclic isomer of the C5H4 family that could be detected via radio astronomy. A computational chemistry study was performed to determine the energies of the five most stable isomers. The isomer (c-C3H3CCH) has a considerably higher energy than the others, and it has not yet been detected. To better understand the chemical reactions involving these species, we compared the ethynyl and cyano derivatives. The observed abundances of these species are in good agreement with the branching ratios of the formation reactions studied with our chemical model of TMC-1.

astro-ph.GA↗

arXiv2024

Discovery of the interstellar cyanoacetylene radical cation HC$_3$N$^+$

We report the first identification in space of HC$_3$N$^+$, the simplest member of the family of cyanopolyyne cations. Three rotational transitions with half-integer quantum numbers from $J$=7/2 to 11/2 have been observed with the Yebes 40m radio telescope and assigned to HC$_3$N$^+$, which has an inverted $^2Π$ ground electronic state. The three rotational transitions exhibit several hyperfine components due to the magnetic and nuclear quadrupole coupling effects of the H and N nuclei. We confidently assign the characteristic rotational spectrum pattern to HC$_3$N$^+$ based on the good agreement between the astronomical and theoretical spectroscopic parameters. We derived a column density of (6.0$\pm$0.6)$\times$10$^{10}$ cm$^{-2}$ and a rotational temperature of 4.5$\pm$1\,K. The abundance ratio between HC$_3$N and HC$_3$N$^+$ is 3200$\pm$320. As found for the larger members of the family of cyanopolyyne cations (HC$_5$N$^+$ and HC$_7$N$^+$), HC$_3$N$^+$ is mainly formed through the reactions of H$_2$ and the cation C$_3$N$^+$ and by the reactions of H$^+$ with HC$_3$N. In the same manner than other cyanopolyyne cations, HC$_3$N$^+$ is mostly destroyed through a reaction with H$_2$ and a dissociative recombination with electrons.

astro-ph.GA↗

arXiv2024

QUIJOTE discovery of the cation radicals HC5N+ and HC7N+

We present the discovery with the QUIJOTE line survey of the cations HC5N+ and HC7N+ in the direction of TMC-1. Seven lines with half-integer quantum numbers from J=25/2-23/2 to 37/2-35/2 have been assigned to HC5N+ and eight lines from J=55/2-53/2 to 71/2-69/2 to HC7N+. Both species have inverted 2Pi ground electronic states with very good estimates for their B0 and AS0 constants based on optical observations. The lines with the lowest J of HC5N+ exhibit multiple components due to the hyperfine structure introduced by the H and N nuclei. However, these different components collapse for the higher J. No hyperfine structure is found for any of the lines of HC7N+. The derived effective rotational and distortion constants for HC5N+ are Beff = 1336.662+/- 0.001 MHz and Deff = 27.4+/-2.6 Hz, while for HC7N+ they are Beff = 567.85036+/-0.00037 MHz and Deff = 4.01+/-0.19 Hz. From the observed intensities, we derived Trot = 5.5+/-0.5K and N = (9.9+/-1.0)x 1010 cm-2 for HC5N+, while we obtained Trot = 8.5+/-0.5K and N = (2.3+/-0.2)x1010 cm-2 for HC7N+. The HC5N/HC5N+, C5N/HC5N+, C5N-/HC5N+, HC7N/HC7N+, HC5N+/HC7N+, and C7N-/HC7N+ abundance ratios are 670+/-80, 4.8+/-0.8, 1.2+/-0.2, 1000+/-150, 4.2+/-0.5, and 2.2+/-0.2, respectively. We have run chemical modelling calculations to investigate the formation and destruction of these new cations. We find that these species are mainly formed through the reactions of H2 and the cations C5N+ and C7N+, and by the reactions of H+ with HC5N and HC7N, while they are mostly destroyed through a reaction with H2 and a dissociative recombination with electrons. Based on the underestimation of the abundances of HC5N+ and HC7N+ by the chemical model by a factor around 20, we suggest that the rate coefficients currently assumed for the reactions of these cations with H2 could be too high by the same factor, something that will be worth investigating.

astro-ph.GA↗

arXiv2024

Laboratory and astronomical discovery of cyanothioketene, NCCHCS, in the cold starless core TMC-1

We present the detection of cyanothioketene, NCCHCS, in the laboratory and toward TMC-1. This transient species was produced through a discharge of a gas mixture of CH2CHCN and CS2 using argon as carrier gas, and its rotational spectrum between 9 and 40 GHz was characterized using a Balle-Flygare narrowband-type Fourier-transform microwave spectrometer. A total of 21 rotational transitions were detected in the laboratory, all of them exhibiting hyperfine structure induced by the spin of the N nucleus. The spectrum for NCCHCS was predicted in the domain of our line surveys using the derived rotational and distortion constants. The detection in the cold starless core TMC-1 was based on the QUIJOTE line survey performed with the Yebes 40m radio telescope. Twenty-three lines were detected with K_a=0, 1, and 2 and J_u=9 up to 14. The derived column density is (1.2+/-0.1)e11 cm-2 for a rotational temperature of 8.5+/-1 K. The abundance ratio of thioketene and its cyano derivative, H2CCS/NCCHCS, is 6.5+/-1.3. Although ketene is more abundant than thioketene by about 15 times, its cyano derivative NCCHCO surprisingly is not detected with a 3sigma upper level to the column density of 3.0e10 cm-2, which results in an abundance ratio H2CCO/NCCHCO > 430. Hence, the chemistry of CN derivatives seems to be more favored for S-bearing than for O-bearing molecules. We carried out chemical modeling calculations and found that the gas-phase neutral-neutral reactions CCN + H2CS and CN + H2CCS could be a source of NCCHCS in TMC-1.

astro-ph.GA↗

arXiv2024

CN and CCH derivatives of ethylene and ethane: Confirmation of the detection of CH$_3$CH$_2$CCH in TMC-1

We present a study of CH$_3$CH$_2$CCH, CH$_3$CH$_2$CN, CH$_2$CHCCH, and CH$_2$CHCN in TMC-1 using the QUIJOTE$^1$ line survey. We confirm the presence of CH$_3$CH$_2$CCH in TMC-1, which was previously reported as tentative by our group. From a detailed study of the ethynyl and cyanide derivatives of CH$_2$CH$_2$ and CH$_3$CH$_3$ in TMC-1, we found that the CH$_2$CHCCH/CH$_2$CHCN and CH$_3$CH$_2$CCH/CH$_3$CH$_2$CN abundance ratios are 1.5$\pm$0.1 and 4.8$\pm$0.5, respectively. The derived CH$_2$CHCCH/CH$_3$CH$_2$CCH abundance ratio is 15.3$\pm$0.8, and that of CH$_2$CHCN over CH$_3$CH$_2$CN is 48$\pm$5. All the single substituted isotopologs of vinyl cyanide have been detected, and we found that the first and second carbon substitutions in CH$_2$CHCN provide a $^{12}$C/$^{13}$C ratio in line with that found for other three-carbon bearing species such as HCCNC and HNCCC. However, the third $^{13}$C isotopolog, CH$_2$CH$^{13}$CN, presents an increase in its abundance similar to that found for HCCCN. Finally, we observed eight $b$-type transitions of CH$_2$CHCN, and we find that their intensity cannot be fitted adopting the dipole moment $μ_b$ derived previously. These transitions involve the same rotational levels as those of the $a$-type transitions. From their intensity, we obtain $μ_b$=0.80$\pm$0.03\,D, which is found to be in between earlier values derived in the laboratory using intensity measurements or the Stark effect. Our chemical model indicates that the abundances of CH$_3$CH$_2$CCH, CH$_3$CH$_2$CN, CH$_2$CHCCH, and CH$_2$CHCN observed in TMC-1 can be explained in terms of gas-phase reactions.

astro-ph.GA↗

arXiv2024

Doubly substituted isotopologues of HCCCN in TMC-1: Detection of D13CCCN, DC13CCN, DCC13CN, DCCC15N, H13C13CCN, H13CC13CN, HC13C13CN, HCC13C15N, and HC13CC15N

We report the first detection in space of a complete sample of nine doubly substituted isotopologues of HCCCN towards the cyanopolyyne peak of TMC-1 using observations of the QUIJOTE line survey taken with the Yebes 40 m telescope. We detected D13CCCN, DC13CCN, DCC13CN, DCCC15N, H13C13CCN, H13CC13CN, HC13C13CN, HCC13C15N, and HC13CC15N through their J=4-3 and J=5-4 lines in the 7 mm window. In addition, we present an extensive analysis of the emission of HCCCN and its singly substituted isotopologues through a large velocity gradient model of the lines detected at 7 mm and 3 mm using the Yebes 40 m and the IRAM 30 m telescopes, respectively. The derived column densities for all the isotopologues are consistent in the two spectral bands for an H2 volume density of 1e4 cm-3 and a kinetic temperature of 10 K. Whereas we observed a 13C fractionation for HCC13CN and other double isotopologues with a 13C atom adjacent to the nitrogen atom, we derived similar C/13C abundance ratios for the three 13C substituted species of DCCCN. This suggests additional chemical discrimination for deuterated isotopologues of HCCCN. Finally, we present the spatial distribution of the J=4-3 and J=5-4 lines from the singly substituted species observed with the Yebes 40 m telescope. The emission peak of the spatial distribution of DCCCN appears to be displaced by 40'' with respect to that of HCCCN and the 13C and 15N isotopologues. In addition to a different formation route for the deuterated species, we could also expect that this differentiation owing to the deuterium fractionation is more efficient at low temperatures, and therefore, that deuterated species trace a colder region of the cloud.

astro-ph.GA↗

arXiv2023

Detection of vibrationally excited C6H in the cold prestellar core TMC-1 with the QUIJOTE line survey

In this work, we present the detection of twelve doublets with quantum numbers of N=12-11 to N=17-16 of the v11 vibrationally excited state of C6H towards TMC-1. This marks the first time that an excited vibrational state of a molecule has been detected in a cold starless core. The data are part of the QUIJOTE line survey gathered with the Yebes 40m radio telescope. The line intensities have been aptly reproduced with a rotational temperature of 6.2 +/- 0.4K and a column density of (1.2+/-0.2)e11 cm-2. We also analysed the ground state transitions of C6H, detecting fourteen lines with quantum numbers of J = 23/2-21/2 to J = 35/2 for each of the two 2Pi_3/2 and 2Pi_1/2 ladders. It is not possible to model the intensities of all the transitions of the ground state simultaneously using a single column density. We considered the two ladders as two different species and found that the rotational temperature is the same for both ladders, Trot(2Pi_3/2)=Trot(2Pi_1/2)=6.2+/-0.2, achieving a result that is comparable to that of the v11 state. The derived column densities are N(2Pi_3/2)(6.2+/-0.3)e12cm-2 and N(2Pi_1/2)=(8.0+/-0.4)e10cm-2. The fraction of C6H molecules in its 2Pi_3/2, 2Pi_1/2, and v11 states is 96.8 %, 1.3 %, and 1.9 %, respectively. Finally, we report that this vibrational mode has also been detected towards the cold cores Lupus-1A and L1495B, as well as the low-mass star forming cores L1527 and L483, with fractions of C6H molecules in this mode of 3.8%, 4.1%, 14.8%, and 6%, respectively.

astro-ph.GA↗