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B. Tercero

Publications and source records attributed to B. Tercero.

At least 55 records · Page 3Linked to original sources

Discovery of interstellar NC4NH+: dicyanopolyynes are indeed abundant in space

The previous detection of two species related to the non polar molecule cyanogen (NCCN), its protonated form (NCCNH+) and one metastable isomer (CNCN), in cold dense clouds supported the hypothesis that dicyanopolyynes are abundant in space. Here we report the first identification in space of NC4NH+, which is the protonated form of NC4N, the second member of the series of dicyanopolyynes after NCCN. The detection was based on the observation of six harmonically related lines within the Yebes 40m line survey of TMC-1 QUIJOTE. The six lines can be fitted to a rotational constant B = 1293.90840 +/- 0.00060 MHz and a centrifugal distortion constant D = 28.59 +/- 1.21 Hz. We confidently assign this series of lines to NC4NH+ based on high-level ab initio calculations, which supports the previous identification of HC5NH+ by Marcelino et al. (2020) from the observation of a series of lines with a rotational constant 2 MHz lower than that derived here. The column density of NC4NH+ in TMC-1 is (1.1 +1.4 -0.6)e10 cm-2, which implies that NC4NH+ is eight times less abundant than NCCNH+. The species CNCN, previously reported toward L483 and tentatively in TMC-1, is confirmed in this latter source. We estimate that NCCN and NC4N are present in TMC-1 with abundances a few times to one order of magnitude lower than HC3N and HC5N, respectively. This means that dicyanopolyynes NC-(CC)n-CN are present at a lower level than the corresponding monocyanopolyynes HCC-(CC)n-CN. The reactions of the radicals CN and C3N with HNC arise as the most likely formation pathways to NCCN and NC4N in cold dense clouds.

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Laboratory and astronomical discovery of magnesium dicarbide, MgC$_2$

We report the detection of magnesium dicarbide, MgC$_2$, in the laboratory at centimeter wavelengths and assign $^{24}$MgC$_2$, $^{25}$MgC$_2$, and $^{26}$MgC$_2$ to 14 unidentified lines in the radio spectrum of the circumstellar envelope of the evolved carbon star IRC+10216. The structure of MgC$_2$ is found to be T-shaped with a highly ionic bond between the metal atom and the C$_2$ unit, analogous to other dicarbides containing electropositive elements. A two-temperature excitation model of the MgC$_2$ emission lines observed in IRC+10216 yields a very low rotational temperature of $6\pm1$ K, a kinetic temperature of $22\pm13$ K, and a column density of $(1.0 \pm 0.3) \times 10^{12}$ cm$^{-2}$. The abundance of MgC$_2$ relative to the magnesium-carbon chains MgCCH, MgC$_4$H, and MgC$_6$H is $1{:}2{:}22{:}20$ and provides a new constraint on the sequential radiative association-dissociative recombination mechanisms implicated in the production of metal-bearing molecules in circumstellar environments.

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Discovery of two new interstellar molecules with QUIJOTE: HCCCHCCC and HCCCCS

We report on the discovery of two new molecules, HCCCHCCC and HCCCCS, towards the starless core TMC-1 in the Taurus region from the QUIJOTE line survey in the 31.1-50.2 GHz frequency range. We identify a total of twenty-nine lines of HCCCHCCC and six rotational transitions of HCCCCS. The rotational quantum numbers range from Ju=10 up to 15 and Ka <=2 for HCCCHCCC and Ju=21/2 up to 31/2 for HCCCCS. We derived a column density for HCCCHCCC of N=(1.3+/-0.2)x10^11 cm-2 with a rotational temperature of 6+/-1 K, while for HCCCCS we derived N=(9.5+/-0.8)x10^10 cm-2 and Trot =10+/-1 K. The abundance of HCCCHCCC is higher than that of its recently discovered isomer, l-H2C6. If we compare HCCCCS with its related molecules, HCS and HCCS, we obtain abundance ratios HCS/HCCCCS=58 and HCCS/HCCCCS=7.2. We investigated the formation of these two molecules using chemical modelling calculations. The observed abundances can be accounted for by assuming standard gas-phase formation routes involving neutral-neutral reactions and ion-neutral reactions.

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Discovery of CH2CCHC4H and a rigorous detection of CH2CCHC3N in TMC-1 with the QUIJOTE line survey

Using the QUIJOTE line survey in the 32.0-50.4 GHz range, we report the discovery of the molecule CH2CCHC4H towards the prestellar cold core TMC-1 in the Taurus region. We also present a rigorous detection of CH2CCHC3N, along with its detailed analysis. We identified a total of twenty rotational transitions for each one of these molecules. The rotational quantum numbers range from Ju=17 up to 24 and Ka<=3. The column density for CH2CCHC4H is N=(2.2+/-0.2)x 1E12 cm-2, while for CH2CCHC3N, we derived N=(1.2+/-0.15) x 1E11 cm-2. The rotational temperature is 9.0+/-0.5 K for both species. The abundance ratio between CH2CCHC4H and CH2CCHC3N is 18+/-4. We also compared the column densities of these species with those of their isomers CH3C6H and CH3C5N, derived from their J=20-19 up to J=30-29 rotational transitions observed with the QUIJOTE line survey. The observed abundances for all these species are reasonably well explained by state-of-the-art chemical models of TMC-1. The observed astronomical frequencies were merged with laboratory frequencies from the literature to derive improved spectroscopic parameters.

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A new protonated molecule discovered in TMC-1: HCCNCH+

In recent years we have seen an important increase in the number of protonated molecules detected in cold dense clouds. Here we report the detection in TMC-1 of HCCNCH+, the protonated form of HCCNC, which is a metastable isomer of HC3N. This is the first protonated form of a metastable isomer detected in a cold dense cloud. The detection was based on observations carried out with the Yebes 40m and IRAM 30m telescopes, which revealed four harmonically related lines. We derive a rotational constant B = 4664.431891 +/- 0.000692 MHz and a centrifugal distortion constant D = 519.14 +/- 4.14 Hz. From a high-level ab initio screening of potential carriers we confidently assign the series of lines to the ion HCCNCH+. We derive a column density of (3.0 +/- 0.5)e10 cm-2 for HCCNCH+, which results in a HCCNCH+/HCCNC abundance ratio of 0.010 +/- 0.002. This value is well reproduced by a state-of-the-art chemical model, which however is subject to important uncertainties regarding the chemistry of HCCNCH+. The observational and theoretical status of protonated molecules in cold dense clouds indicate that there exists a global trend in which protonated-to-neutral abundance ratios MH+/M increase with increasing proton affinity of the neutral M, although if one restricts to species M with high proton affinities (>700 kJ/mol), MH+/M ratios fall in the range 0.001-0.1, with no apparent correlation with proton affinity. We suggest various protonated molecules that are good candidates for detection in cold dense clouds in the near future.

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Discovery of a new molecular ion, HC7NH+, in TMC-1

We report the detection of the protonated form of HC7N in TMC-1. The discovery of the cation HC7NH+ was carried out via the observation of nine harmonically related lines in the Q-band using the Yebes 40m radiotelescope. The observed frequencies allowed us to obtain the rotational constants B_0=553.938802(160)MHz and D_0=3.6292(705) Hz. The identification of HC7NH+ is further supported by accurate ab initio calculations. We derived a column density of (5.5+/-0.7)e10 cm-2, which constitutes another piece of evidence for the identification of the carrier. In addition, we revised the HC7N column density and we derived a new value of (2.1+/-0.2)e13cm-2. Hence, the abundance ratio HC7N/HC7NH+ is 380, while those for HC3N/HC3NH+ and HC5N/HC5NH+ are 230 and 240, respectively. Here, we discuss these results within the framework of a chemical model for protonated molecules in cold dense clouds.

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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.

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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.

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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.

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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.

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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.

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Ultra-deep 31.0-50.3 GHz spectral survey of IRC+10216

Context. IRC+10216, the carbon-rich envelope of the asymptotic giant branch (AGB) star CW Leo, is one of the richest molecular sources in the sky. Available spectral surveys below 51 GHz are more than 25 years old and new work is needed. Aims. Characterizing the rich molecular content of this source, specially for heavy species, requires to carry out very sensitive spectral surveys at low frequencies. In particular in this work we have achieved an rms in the range 0.2-0.6 mK per MHz. Methods. long Q-band (31.0-50.3 GHz) single dish integrations were carried out with the Yebes 40m telescope using specifically built receivers. State of the art line catalogs are used for line identification. Results. A total of 652 spectral features corresponding to 713 transitions from 81 species (we count as different the isomers, isotopologues and ortho/para species) are present in the data. Only 57 unidentified lines remain with signal to noise ratios >3. Some new species and/or vibrational modes have been discovered for the first time with this survey. Conclusions. This IRC+10216 spectral survey is, by far, the most sensitive one carried out to this date in the Q-band. It therefore provides the most complete view of IRC+10216 from 31.0 to 50.3 GHz, giving unique information on its molecular content, specially for heavy species. Rotational diagrams built from the data provide valuable information on the physical conditions and chemical content of this circumstellar envelope.

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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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First detection of C$_2$H$_5$NCO in the ISM and search of other isocyanates towards the G+0.693-0.027 molecular cloud

Little is known about the chemistry of isocyanates (compounds with the functional group R-N=C=O) in the interstellar medium, as only four of them have been detected so far: isocyanate radical (NCO), isocyanic acid (HNCO), N-protonated isocyanic acid (H$_2$NCO$^+$) and methyl isocyanate (CH$_3$NCO). The molecular cloud G+0.693-0.027, located in the Galactic Centre, represents an excellent candidate to search for new isocyanates since it exhibits high abundances of the simplest ones, HNCO and CH$_3$NCO. After CH$_3$NCO, the next complex isocyanates are ethyl isocyanate (C$_2$H$_5$NCO) and vinyl isocyanate (C$_2$H$_3$NCO). Their detection in the ISM would enhance our understanding of the formation of these compounds in space. We have detected C$_2$H$_5$NCO and H$_2$NCO$^+$ towards G+0.693-0.027 (the former for the first time in the interstellar medium) with molecular abundances of (4.7$-$7.3)$\times$10$^{-11}$ and (1.0$-$1.5)$\times$10$^{-11}$, respectively. A ratio CH$_3$NCO / C$_2$H$_5$NCO = 8$\pm$1 is obtained; therefore the relative abundance determined for HNCO:CH$_3$NCO:C$_2$H$_5$NCO is 1:1/55:1/447, which implies a decrease by more than one order of magnitude going progressively from HNCO to CH$_3$NCO and to C$_2$H$_5$NCO. This is similar to what has been found for e.g. alcohols and thiols and suggests that C$_2$H$_5$NCO is likely formed on the surface of dust grains. In addition, we have obtained column density ratios of HNCO / NCO > 269, HNCO / H$_2$NCO$^+$ $\sim$ 2100 and C$_2$H$_3$NCO / C$_2$H$_5$NCO~<~4. A comparison of the Methyl~/~Ethyl ratios for isocyanates (-NCO), alcohols (-OH), formiates (HCOO-), nitriles (-CN) and thiols (-SH) is performed and shows that ethyl-derivatives may be formed more efficiently for the N-bearing molecules than for the O- and S-bearing molecules.

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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.

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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.

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Detection of the cyanomidyl radical (HNCN): a new interstellar species with the NCN backbone

We report here the first detection in the interstellar medium of the cyanomidyl radical (HNCN). Using the Yebes 40m and the IRAM 30m telescopes, we have targeted the doublets of the $N$=2$-$1, 4$-$3, 5$-$4, 6$-$5, and 7$-$6 transitions of HNCN toward the molecular cloud G+0.693-0.027. We have detected three unblended lines of HNCN, these are the $N$=6$-$5 doublet and one line of the $N$=4$-$3 transition. Additionally we present one line of the $N$=5$-$4 transition partially blended with emission from other species. The Local Thermodynamic Equilibrium best fit to the data gives a molecular abundance of (0.91$\pm$0.05)$\times$10$^{-10}$ with respect to H$_2$. The relatively low abundance of this species in G+0.693-0.027, and its high reactivity, suggest that HNCN is possibly produced by gas-phase chemistry. Our work shows that this highly reactive molecule is present in interstellar space, and thus it represents a plausible precursor of larger prebiotic molecules with the NCN backbone such as cyanamide (NH$_2$CN), carbodiimide (HNCNH) and formamidine (NH$_2$CHNH).

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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.

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