arXiv subjects

A. Belloche

Publications and source records attributed to A. Belloche.

At least 37 records · Page 2Linked to original sources

arXiv2022

Millimetre-wave spectroscopy of 2-hydroxyprop-2-enal and an astronomical search with ALMA

The molecule studied in this work, 2-hydroxyprop-2-enal, is among the candidates to be searched for in the interstellar medium (ISM), as it is a dehydration product of C3 sugars and contains structural motifs typical for some interstellar molecules. The aim of this work is to deepen knowledge about the millimetre-wave spectrum of 2-hydroxyprop-2-enal in the region enabling its search towards astronomical objects. We target the solar-type protostar IRAS16293-2422 and star-forming region Sagittarius (Sgr) B2(N). The rotational spectrum of 2-hydroxyprop-2-enal was measured and analysed in the frequency regions of 128-166 GHz and 285-329 GHz. The interstellar exploration towards IRAS16293-2422 was based on the Atacama Large Millimeter/submillimeter Array (ALMA) data of the Protostellar Interferometric Line Survey. We also used the imaging spectral line survey ReMoCA performed with ALMA toward Sgr B2(N). We modelled the astronomical spectra under the assumption of local thermodynamic equilibrium. We provide analysis of hundreds of rotational transitions of 2-hydroxyprop-2-enal in the ground state and the lowest lying excited vibrational state. We report its nondetection towards IRAS16293 B. The 2-hydroxyprop-2-enal/3-hydroxypropenal abundance ratio is estimated to be less-than or similar to 0.9-1.3 in agreement with the predicted value of 1.4. We also report the nondetection of 2-hydroxyprop-2-enal toward the hot molecular core Sgr B2(N1). We did not detect the related aldehydes 2-hydroxypropanal and 3-hydroxypropenal either. We find that these three molecules are at least 9, 4, and 10 times less abundant than acetaldehyde in this source, respectively. Despite the nondetections, the results of this work represent a significant improvement on previous investigations in the microwave region and meets the requirements for further searches of this molecule in the ISM.

astro-ph.GA↗

arXiv2022

Millimeter wave spectrum and search for vinyl isocyanate toward Sgr B2(N) with ALMA

The interstellar detections of isocyanic acid, methyl isocyanate, and very recently also ethyl isocyanate, open the question of the possible detection of vinyl isocyanate in the interstellar medium. The aim of this study is to extend the laboratory rotational spectrum of vinyl isocyanate into the millimeter wave region and to undertake a check for its presence in the high-mass star forming region Sgr B2. The rotational spectrum of vinyl isocyanate was recorded in the frequency regions 127.5-218 and 285-330 GHz using the Prague millimeter wave spectrometer. The spectral analysis was supported by high-level quantum-chemical calculations. We assumed local thermodynamic equilibrium to compute synthetic spectra of vinyl isocyanate and to search for it in the ReMoCA survey performed with ALMA toward Sgr B2(N). We also searched for ethyl isocyanate in the same source. Accurate values for the rotational and centrifugal distortion constants are reported for the ground vibrational states of trans and cis vinyl isocyanate. We report nondetections of vinyl and ethyl isocyanate toward the main hot core of Sgr B2(N). We find that vinyl and ethyl isocyanate are at least 11 and 3 times less abundant than methyl isocyanate in this source, respectively. Although the precise formation mechanism of interstellar methyl isocyanate itself remains uncertain, we infer from existing astrochemical models that our observational upper limit for the CH3NCO:C2H5NCO ratio in Sgr B2(N) is consistent with ethyl isocyanate being formed on dust grains via the abstraction or photodissociation of an H atom from methyl isocyanate, followed by the addition of a methyl radical. The dominance of such a process for ethyl isocyanate production, combined with the absence of an analogous mechanism for vinyl isocyanate, would indicate that the ratio C2H3NCO:C2H5NCO should be rather less than unity.

astro-ph.GA↗

arXiv2022

Rotational spectroscopy $n$-propanol: $Aa$ and $Ag$ conformers

The primary alcohol $n$-propanol (i.e., $normal$-propanol or propan-1-ol; C$_3$H$_7$OH) occurs in five different conformers: $Ga$, $Gg$, $Gg'$, $Aa$, and $Ag$. All rotational spectra of the three conformers of the $G$ family are well described, making astronomical search of their spectroscopic signatures possible, as opposed to those of the $Aa$ and $Ag$ conformers. Our goal is to facilitate the astronomical detection of $Aa$ and $Ag$ conformers of $n$-propanol by characterizing their rotational spectra. We recorded the rotational spectra of $n$-propanol in the frequency domain of 18$-$505\,GHz.Additional double-modulation double-resonance (DM-DR) measurements were performed, more specifically with the goal to unambiguously assign weak transitions of the $Aa$ conformer and to verify assignments of the $Ag$ conformer. We derived a spectroscopic quantum mechanical model with experimental accuracy (with $J_\textrm{max}=70$ and $K_{a,\textrm{max}}=6$) for $Aa$ $n$-propanol. Furthermore, we unambiguously assigned transitions (with $J_\textrm{max}=69$ and $K_{a,\textrm{max}}=9$) of $Ag$ $n$-propanol; in doing so, we prove the existence of two tunneling states, $Ag^+$ and $Ag^-$. The astronomical search of all five conformers of $n$-propanol is now possible via their rotational signatures. These are applied in a companion article on the detection of $n$-propanol toward the hot molecular core Sgr B2(N2).

physics.chem-ph↗

arXiv2022

Interstellar detection and chemical modeling of iso-propanol and its normal isomer

The detection of a branched alkyl molecule in the high-mass star forming protocluster Sgr B2(N) permitted by the advent of ALMA revealed a new dimension of interstellar chemistry. Astrochemical simulations subsequently predicted that beyond a certain degree of molecular complexity, branched molecules could even dominate over their straight-chain isomers. More generally, we aim at probing further the presence in the ISM of complex organic molecules with the capacity to exhibit both a normal and iso form, via the attachment of a functional group to either a primary or secondary carbon atom. We used the imaging spectral line survey survey ReMoCA performed with ALMA and the results of a recent spectroscopic study of propanol to search for the iso and normal isomers of this molecule in the hot molecular core Sgr B2(N2). We expanded the network of the astrochemical model MAGICKAL to explore the formation routes of propanol. We report the first interstellar detection of iso-propanol toward a position of Sgr B2(N2) that shows narrow linewidths. We also report the first secure detection of normal-propanol in a hot core. i-Propanol is found to be nearly as abundant as n-propanol, with an abundance ratio of 0.6 similar to the ratio of 0.4 that we obtained previously for i- and n-propyl cyanide in Sgr B2(N2). The results are in good agreement with the outcomes of our astrochemical models, which indicate that OH-radical addition to propylene in dust-grain ice mantles, driven by water photodissociation, can produce appropriate quantities of n- and i-propanol. The n-to-i ratio in Sgr B2(N2) may be a direct inheritance of the branching ratio of this reaction process. The detection of n- and i-propanol and their ratio indicate that the modest preference toward the normal form of propyl cyanide determined previously may be a more general feature among similarly sized interstellar molecules. [abridged]

astro-ph.GA↗

arXiv2022

Toward the limits of complexity of interstellar chemistry: Rotational spectroscopy and astronomical search for n- and i-butanal

In recent times, large organic molecules of exceptional complexity have been found in diverse regions of the interstellar medium. In this context, we aim to provide accurate frequencies of the ground vibrational state of two key aliphatic aldehydes, n-butanal and its branched-chain isomer, i-butanal, to enable their eventual detection in the interstellar medium. We employ a frequency modulation millimeter-wave absorption spectrometer to measure the rotational features of n- and i-butanal. We use the spectral line survey ReMoCA performed with the Atacama Large Millimeter/submillimeter Array to search for n- and i-butanal toward the star-forming region Sgr B2(N). We also search for both aldehydes toward the molecular cloud G+0.693-0.027 with IRAM 30 m and Yebes 40 m observations. Several thousand rotational transitions belonging to the lowest-energy conformers have been assigned in the laboratory spectra up to 325 GHz. A precise set of the relevant rotational spectroscopic constants has been determined for each structure. We report non-detections of n- and i-butanal toward both sources, Sgr B2(N1S) and G+0.693-0.027. We find that n- and i-butanal are at least 2-6 and 6-18 times less abundant than acetaldehyde toward Sgr B2(N1S), respectively, and that n-butanal is at least 63 times less abundant than acetaldehyde toward G+0.693-0.027. Comparison with astrochemical models indicates good agreement between observed and simulated abundances (where available). Grain-surface chemistry appears sufficient to reproduce aldehyde ratios in G+0.693-0.027; gas-phase production may play a more active role in Sgr B2(N1S). Our astronomical results indicate that the family of interstellar aldehydes in the Galactic center region is characterized by a drop of one order of magnitude in abundance at each incrementation in the level of molecular complexity.

astro-ph.GA↗

arXiv2022

Sulphur-rich cold gas around the hot core precursor G328.2551-0.5321. An APEX unbiased spectral survey of the 2 mm, 1.2 mm, and 0.8 mm atmospheric windows

During star formation, the dense gas undergoes significant chemical evolution leading to the emergence of a rich variety of molecules associated with hot cores and hot corinos. The physical and chemical conditions are poorly constrained; the early phases of emerging hot cores in particular represent an unexplored territory. We provide here a full molecular inventory of a massive protostellar core that is proposed to be a precursor of a hot core. We performed an unbiased spectral survey towards the hot core precursor associated with clump G328.2551-0.5321 between 159GHz and 374GHz. To identify the spectral lines, we used rotational diagrams and radiative transfer modelling assuming LTE. We detected 39 species and 26 isotopologues, and were able to distinguish a warm and compact inner region, a colder more extended envelope, and the kinematic signatures of the accretion shocks that have previously been observed with ALMA. We associate most of the emission of the small molecules with the cold gas, while the molecular emission of the warm gas is enriched by complex organic molecules (COMs). We find a high abundance of S-bearing molecules in the cold gas phase suggesting a low sulphur depletion, with a factor of > 1%. We identify nine COMs in the warm gas, four in the cold gas, and four towards the accretion shocks. The high abundances of S-bearing species originating from the undisturbed gas may suggest a contribution from shocked gas at the outflow cavity walls. The molecular composition of the warm gas is similar to that of both hot cores and hot corinos, but the molecular abundances are closer to the values found towards hot corinos than to values found towards hot cores. Considering the compactness of the warm region and its moderate temperature, we suggest that thermal desorption has not been completed towards this object yet, representing an early phase of the emergence of hot cores.

astro-ph.GA↗

arXiv2021

Expanding the submillimeter wave spectroscopy and astronomical search for thioacetamide (CH3CSNH2) in the ISM

Thioacetamide (CH3CSNH2) is the sulfur analog to acetamide (CH3CONH2) and it is a viable candidate to search for in astronomical environments specifically toward regions where other S-bearing molecules have been found and, if possible, that also contain a detection of CH3CONH2. If detected, it would not only continue to expand the view of molecular complexity in astronomical environments, but also help to better elucidate the possible formation pathways of these types of species in these environments. The rotational spectrum of CH3CSNH2 was investigated up to 650 GHz. Using the newly refined spectrum of CH3CSNH2, as well as additional spectroscopic data on the chemically related species CH3CONH2, a variety of astronomical sources were searched including data from the following large surveys: The PRIMOS conducted with the Green Bank Telescope (GBT); Exploring molecular complexity with ALMA (EMoCA) conducted with ALMA; and Astrochemical Surveys at IRAM (ASAI) conducted with the Institut de Radioastronomie Millimetrique (IRAM) 30m Telescope. A total of 1428 transitions from the vt=0 state with maximum values J=47 and Ka=20 in the range up to 330 GHz, and J=95 and Ka=20 in the range from 400 - 660 GHz were assigned. We also assigned 321 transitions from the vt=1 state with the maximum values J=35 and Ka=9 up to 330 GHz. The final fit is based on the rho-axis-method (RAM) Hamiltonian model that includes 40 parameters. An astronomical search for CH3CSNH2 was conducted based on all the new spectroscopic data. No transitions of CH3CSNH2 were detected toward any of the sources contained in our survey. Using the appropriate telescope and physical parameters for each astronomical source, upper limits to the column densities were found for CH3CSNH2 toward each source.

astro-ph.GA↗

arXiv2021

Laboratory rotational spectroscopy of acrylamide and search for acrylamide and propionamide toward Sgr B2(N) with ALMA

Numerous complex organic molecules have been detected in the universe among which amides are considered as models for species containing the peptide linkage. Acrylamide bears in its backbone not only the peptide bond, but also the vinyl functional group which is a common motif in many interstellar compounds. This makes acrylamide an interesting target for a search in space. In addition, a tentative detection of the related molecule propionamide has been recently claimed toward Sgr B2(N). We report accurate laboratory measurements and analyses of thousands rotational transitions for the syn and skew forms of acrylamide between 75 and 480 GHz. Tunneling through a low energy barrier between two symmetrically equivalent configurations has been revealed for the higher-energy skew species. We searched for emission of acrylamide in the imaging spectral line survey ReMoCA performed with ALMA toward Sgr B2(N). We also searched for propionamide in the same source. Neither acrylamide nor propionamide were detected toward the two main hot molecular cores of Sgr B2(N). We did not detect propionamide either toward a position located to the east of the main hot core, thereby not confirming the recent claim of its interstellar detection toward this position. We find that acrylamide and propionamide are at least 26 and 14 times, respectively, less abundant than acetamide toward the main hot core Sgr B2(N1S), and at least 6 and 3 times, respectively, less abundant than acetamide toward the secondary hot core Sgr B2(N2). A comparison with results of astrochemical kinetics model for related species suggests that acrylamide may be a few hundred times less abundant than acetamide, corresponding to a value at least an order of magnitude lower than the observational upper limits. Propionamide may be as little as only a factor of two less abundant than the upper limit derived toward Sgr B2(N1S).

astro-ph.GA↗

arXiv2021

Millimetre-wave laboratory study of glycinamide and search for it with ALMA toward Sagittarius B2(N)

Glycinamide is considered to be one of the possible precursors of the simplest amino acid glycine. Its only rotational spectrum reported so far has been in the cm-wave region. The aim of this work is to extend its laboratory spectrum into the mm wave region to support its searches in the ISM. Glycinamide was synthesised chemically and was studied with broadband rotational spectroscopy in the 90-329 GHz region. Tunneling across a low energy barrier between two symmetry equivalent configurations of the molecule resulted in splitting of each vibrational state and many perturbations in associated rotational energy levels, requiring careful coupled state fits for each vibrational doublet. We searched for emission of glycinamide in the imaging spectral line survey ReMoCA performed with ALMA toward Sgr B2(N). We report the first analysis of the mm-wave rotational spectrum of glycinamide, resulting in fitting to experimental measurement accuracy of over 1200 transition frequencies for the ground state tunneling doublet, of many lines for tunneling doublets for two singly excited vibrational states, and determination of precise vibrational separation in each doublet. We did not detect emission from glycinamide in the hot core Sgr B2(N1S). We found that glycinamide is at least seven times less abundant than aminoacetonitrile and 1.8 times less abundant than urea in this source. A comparison with results of astrochemical kinetics models for species related to glycinamide suggests that its abundance may be at least one order of magnitude below the upper limit obtained toward Sgr B2(N1S). This means that glycinamide emission in this source likely lies well below the spectral confusion limit in the frequency range covered by the ReMoCA survey. Targetting sources with a lower level of spectral confusion, such as the Galactic Center shocked region G+0.693-0.027, may be a promising avenue. [abridged]

astro-ph.GA↗

arXiv2021

Rotational spectroscopic study and astronomical search for propiolamide in Sgr B2(N)

For all the amides detected in the interstellar medium (ISM), the corresponding nitriles or isonitriles have also been detected in the ISM, some of which have relatively high abundances. Among the abundant nitriles for which the corresponding amide has not yet been detected is cyanoacetylene (HCCCN), whose amide counterpart is propiolamide (HCCC(O)NH$_2$). With the aim of supporting searches for this amide in the ISM, we provide a complete rotational study of propiolamide from 6 GHz to 440 GHz using rotational spectroscopic techniques in the frequency and time domain. We identified and measured more than 5500 distinct frequency lines of propiolamide and obtained accurate sets of spectroscopic parameters for the ground state and the three low-lying excited vibrational states. We used the ReMoCA spectral line survey performed with the Atacama Large Millimeter/submillimeter Array toward the star-forming region Sgr B2(N) to search for propiolamide. We report the nondetection of propiolamide toward the hot cores Sgr B2(N1S) and Sgr B2(N2). We find that propiolamide is at least 50 and 13 times less abundant than acetamide in Sgr B2(N1S) and Sgr B2(N2), respectively, indicating that the abundance difference between both amides is more pronounced by at least a factor of 8 and 2, respectively, than for their corresponding nitriles. Although propiolamide has yet to be included in astrochemical modeling networks, the observed upper limit to the ratio of propiolamide to acetamide seems consistent with the ratios of related species as determined from past simulations.

astro-ph.GA↗

arXiv2021

The CALYPSO IRAM-PdBI survey of jets from Class 0 protostars. Are jets ubiquitous in young stars ?

As a part of the CALYPSO large programme, we constrain the properties of protostellar jets and outflows in a sample of 21 Class 0 protostars with internal luminosities, Lint, from 0.035 to 47 Lsun. We analyse high angular resolution (~0.5"-1") IRAM PdBI observations in CO (2-1), SO ($5_6-4_5$), and SiO (5-4). CO (2-1), which probes outflowing gas, is detected in all the sources (for the first time in SerpS-MM22 and SerpS-MM18b). Collimated high-velocity jets in SiO (5-4) are detected in 67% of the sources (for the first time in IRAS4B2, IRAS4B1, L1448-NB, SerpS-MM18a), and 77% of these also show jet/outflow emission in SO ($5_6-4_5$). In 5 sources (24% of the sample) SO ($5_6-4_5$) probes the inner envelope and/or the disk. The CALYPSO survey shows that the outflow phenomenon is ubiquitous and that the detection rate of high-velocity jets increases with protostellar accretion, with at least 80% of the sources with Lint>1 Lsun driving a jet. The protostellar flows exhibit an onion-like structure, where the SiO jet (opening angle ~10$^o$) is nested into a wider angle SO (~15$^o$) and CO (~25$^o$) outflow. On scales >300 au the SiO jets are less collimated than atomic jets from Class II sources (~3$^o$). Velocity asymmetry between the two jet lobes are detected in one third of the sources, similarly to Class II atomic jets, suggesting that the same launching mechanism is at work. Most of the jets are SiO rich (SiO/H2 from >2.4e-7 to >5e-6), which indicates efficient release of >1%-10% of silicon in gas phase likely in dust-free winds, launched from inside the dust sublimation radius. The mass-loss rates (from ~7e-8 to ~3e-6 Msun/yr) are larger than what was measured for Class II jets. Similarly to Class II sources, the mass-loss rates are ~1%-50% of the mass accretion rates suggesting that the correlation between ejection and accretion in young stars holds from 1e4 yr up to a few Myr.

astro-ph.SR↗

arXiv2021

Physical and chemical structure of the Serpens filament -- fast formation and gravity-driven accretion

The Serpens filament, a prominent elongated structure in a relatively nearby molecular cloud, is believed to be at an early evolutionary stage, so studying its physical and chemical properties can shed light on filament formation and early evolution. The main goal is to address the physical and chemical properties as well as the dynamical state of the Serpens filament at a spatial resolution of $\sim$0.07 pc and a spectral resolution of $\lesssim$0.1~km~s$^{-1}$. We performed $^{13}$CO (1--0), C$^{18}$O (1--0), C$^{17}$O (1--0), $^{13}$CO (2--1), C$^{18}$O (2--1), and C$^{17}$O (2--1) imaging observations toward the Serpens filament with the Institut de Radioastronomie Millim{é}trique 30-m (IRAM-30 m) and Atacama Pathfinder EXperiment (APEX) telescopes. Widespread narrow $^{13}$CO (2--1) self-absorption is observed in this filament, causing the $^{13}$CO morphology to be different from the filamentary structure traced by C$^{18}$O and C$^{17}$O. Our excitation analysis suggests that the opacities of C$^{18}$O transitions become higher than unity in most regions, and this analysis confirms the presence of widespread CO depletion. Further we show that the local velocity gradients have a tendency to be perpendicular to the filament's long axis in the outskirts and parallel to the large-scale magnetic field direction. The magnitudes of the local velocity gradients decrease toward the filament's crest. The observed velocity structure can be a result of gravity-driven accretion flows. The isochronic evolutionary track of the C$^{18}$O freeze-out process indicates the filament is young with an age of $\lesssim$2 Myr. We propose that the Serpens filament is a newly-formed slightly-supercritical structure which appears to be actively accreting material from its ambient gas.

astro-ph.GA↗

arXiv2020

Probing episodic accretion with chemistry: CALYPSO observations of IRAM 04191+1522. Results from the CALYPSO IRAM-PdBI survey

Context. The process of mass accretion in the earliest phases of star formation is still not fully understood: Does the accretion rate smoothly decline with the age of the protostar or are there short, intermittent accretion bursts? Aims. We aim to explore whether or not the observed C$^{18}$O and N$_2$H$^+$ emission pattern towards the VeLLO IRAM 04191+1522 can be understood in the framework of a scenario where the emission is chemically tracing a past accretion burst. Methods.We used high-angular-resolution Plateau de Bure Interferometer (PdBI) observations of C$^{18}$O and N$_2$H$^+$ towards IRAM 04191+1522 that were obtained as part of the CALYPSO IRAM Large Program. We model these observations using a chemical code with a time-dependent physical structure coupled with a radiative transfer module, where we allow for variations in the source luminosity. Results. We find that the N$_2$H$^+$ line emission shows a central hole, while the C$^{18}$O emission is compact. The morphology of these two lines cannot be reproduced with a constant luminosity model based on the present-day internal luminosity (0.08 L$_{sun}$). However, the N$_2$H$^+$ peaks are consistent with a constant-luminosity model of 12 L$_{sun}$. Using a model with time-dependent temperature and density profiles, we show that the observed N$_2$H$^+$ peak emission could indeed be caused by a past accretion burst. Such a burst should have occurred a couple of hundred years ago. Conclusions. We suggest that an accretion burst occurred in IRAM 04191+1522 in the recent past. If such bursts are common and sufficiently long in VeLLOs, they could lead to higher accretion onto the central object than their luminosity suggests. For IRAM 04191 in particular, our results yield an estimated final mass of 0.2 - 0.25 M$_{sun}$ by the end of the Class 0 phase, which would make this object a low-mass star rather than a brown dwarf.

astro-ph.SR↗

arXiv2020

Sulphur and carbon isotopes towards Galactic centre clouds

Measuring isotopic ratios is a sensitive technique used to obtain information on stellar nucleosynthesis and chemical evolution. We present measurements of the carbon and sulphur abundances in the interstellar medium of the central region of our Galaxy. The selected targets are the +50km/s Cloud and several l.o.s. clouds towards Sgr B2(N). Towards the +50km/s Cloud, we observed the J=2-1 rotational transitions of CS, C34S, 13CS, C33S, and 13C34S, and the J=3-2 transitions of CS and C34S with the IRAM-30m telescope, as well as the J=6-5 transitions of C34S and 13CS with the APEX 12m telescope, all in emission. The J=2-1 rotational transitions of CS, C34S, 13CS, and 13C34S were observed with ALMA in the envelope of Sgr B2(N), with those of CS and C34S also observed in the l.o.s. clouds towards Sgr B2(N), all in absorption. In the +50km/s Cloud we derive a 12C13C isotopic ratio of ~22.1, that leads, with the measured 13CS/C34S line intensity ratio, to a 32S/34S ratio of 16.3+3.0-2.4. We also derive the 32S/34S isotopic ratio more directly from the two isotopologues 13CS and 13C34S, which leads to an independent 32S/34S estimation of 16.3+2.1-1.7 and 17.9+-5.0 for the +50km/s Cloud and Sgr B2(N), respectively. We also obtain a 34S/33S ratio of ~4.3 in the +50 km/s Cloud. Previous studies observed a decreasing trend in the 32S/34S isotopic ratios when approaching the Galactic centre. Our result indicates a termination of this tendency at least at a galactocentric distance of 130-30+60 pc. This is at variance with findings based on 12C/13C, 14N/15N and 18O/17O isotope ratios, where the above-mentioned trend is observed to continue right to the central molecular zone. This can indicate a drop in the production of massive stars at the Galactic centre, in the same line as recent metallicity gradient studies, and opens the work towards a comparison with Galactic and stellar evolution models.

astro-ph.GA↗

arXiv2020

Millimeter- and submillimeter-wave spectroscopy of thioformamide and interstellar search toward Sgr B2(N)

Thioformamide NH2CHS is a sulfur-bearing analog of formamide NH2CHO. The latter was detected in the interstellar medium back in the 1970s. Most of the sulfur-containing molecules detected in the interstellar medium are analogs of corresponding oxygen-containing compounds. Therefore, thioformamide is an interesting candidate for a search in the interstellar medium. The rotational spectrum of thioformamide was measured and analyzed in the frequency range 150 to 660 GHz using the Lille spectrometer. We searched for thioformamide toward the high-mass star-forming region Sagittarius (Sgr) B2(N) using the ReMoCA spectral line survey carried out with the Atacama Large Millimeter/submillimeter Array (ALMA). Accurate rotational constants were obtained from the analysis of the ground state of parent, 34S, 13C, and 15N singly substituted isotopic species of thioformamide. For the parent isotopolog, the lowest two excited vibrational states, v12 = 1 and v9 = 1, were analyzed using a model that takes Coriolis coupling into account. Thioformamide was not detected toward the hot cores Sgr B2(N1S) and Sgr B2(N2). The sensitive upper limits indicate that thioformamide is nearly three orders of magnitude at least less abundant than formamide. This is markedly different from methanethiol, which is only about two orders of magnitude less abundant than methanol in both sources. The different behavior shown by methanethiol versus thioformamide may be caused by the preferential formation of the latter (on grains) at late times and low temperatures, when CS abundances are depressed. This reduces the thioformamide-to-formamide ratio, because the HCS radical is not as readily available under these conditions.

astro-ph.GA↗

arXiv2020

Interstellar glycolamide: A comprehensive rotational study and an astronomical search in Sgr B2(N)

Glycolamide is a glycine isomer and also one of the simplest derivatives of acetamide (e.g., one hydrogen atom is replaced with a hydroxyl group), which is a known interstellar molecule. Using a battery of state of the art rotational spectroscopic techniques in the frequency and time domain, around 1500 transitions have been newly assigned. Based on the reliable frequency predictions, we report a radioastronomical search for glycolamide in the well known high-mass star forming region Sgr B2(N) using the ALMA imaging spectral line survey ReMoCA. We also searched for glycolamide toward Sgr B2(N) with the Effelsberg radio telescope. We report the nondetection of glycolamide toward this source with an abundance at least six and five times lower than that of acetamide and glycolaldehyde, respectively. Our astrochemical model suggests that glycolamide may be present in this source at a level just below the upper limit, which was derived from the EMoCA survey. We could also not detect the molecule in the region's extended molecular envelope, which was probed with the Effelsberg telescope. We find an upper limit to its column density that is similar to the column densities obtained earlier for acetamide and glycolaldehyde with the Green Bank Telescope.

astro-ph.GA↗

arXiv2020

Far-infrared laboratory spectroscopy of aminoacetonitrile and first interstellar detection of its vibrationally excited transitions

Aminoacetonitrile, a molecule detected in the interstellar medium only towards the star-forming region Sagittarius B2 (Sgr B2) thus far, is considered an important prebiotic species. To date, observations were limited to ground state emission lines, whereas transitions from within vibrationally excited states remained undetected. We wanted to accurately determine the energies of the low-lying vibrational states of aminoacetonitrile, which are expected to be populated in Sgr B2(N1), the main hot core of Sgr B2(N). This step is fundamental in order to properly evaluate the vibration-rotation partition function of aminoacetonitrile as well as the line strengths of the rotational transitions of its vibrationally excited states. This is necessary to derive accurate column densities and secure the identification of these transitions in astronomical spectra. The far-infrared ro-vibrational spectrum of aminoacetonitrile has been recorded in absorption against a synchrotron source of continuum emission. Three bands, corresponding to the lowest vibrational modes of aminoacetonitrile, were observed in the frequency region below 500 cm$^{-1}$. The combined analysis of ro-vibrational and pure rotational data allowed us to prepare new spectral line catalogs for all the states under investigation. We used the imaging spectral line survey ReMoCA performed with ALMA to search for vibrationally excited aminoacetonitrile toward Sgr B2(N1). On the basis of these spectroscopic predictions, we report the interstellar detection of aminoacetonitrile in its $v_{11}=1$ and $v_{18}=1$ vibrational states toward Sgr B2(N1) in addition to emission in its vibrational ground state. The intensities of the identified $v_{11}=1$ and $v_{18}=1$ lines are consistent with the detected $v=0$ lines under LTE at a temperature of 200 K for an aminoacetonitrile column density of $1.1 \times 10^{17}$ cm$^{-2}$.

astro-ph.GA↗

arXiv2020

Molecular remnant of Nova 1670 (CK Vulpeculae): I. Properties and enigmatic origin of the gas

CK Vul erupted in 1670 and is considered a stellar-merger candidate. Its remnant contains a molecular component of surprisingly rich composition. We present interferometric line surveys with subarcsec resolution with ALMA and SMA. The observations provide interferometric maps of molecular line emission at frequencies between 88 and 243 GHz that allow imaging spectroscopy of more than 180 transitions of 26 species. We present, classify, and analyze the different morphologies of the emission regions displayed by the molecules. We also perform a non-LTE radiative-transfer analysis of emission of most of the observed species, deriving temperatures and column densities in five parts of the nebula. Non-LTE effects are clearly seen in complex species including methanol absorption against the CMB. The temperatures are 17 K in the inner remnant and 14 K in the extended lobes. We find total (hydrogen plus helium) densities in the range of $10^4-10^6$ cm$^{-3}$. The column densities provide relative abundance patterns in the remnant which currently are not understood. Attempts to derive elemental abundances within the assumption of a chemical equilibrium give only loose constraints on the CNO elements. That the formation of many of the observed molecules requires a major involvement of circumstellar shocks remains the preferred possibility. The molecular gas could have formed 350 yr ago or more recently. The molecules are well shielded from the interstellar radiation field by the circumstellar dust. Their presence alone indicates that the unobservable central star cannot be a hot object such as a white dwarf. This excludes some of the proposed scenarios on the nature of CK Vul. The general characteristics of the molecular environment of CK Vul derived in this study resemble quite well those of some pre-planetary nebulae and AGB stars, most notably that of OH231.8.

astro-ph.SR↗