Search

There is evidence that the star formation process is linked to the intricate net of filaments in molecular clouds, which may be also due to gas compression from external triggers. We studied the southern region of the Perseus NGC 1333 molecular cloud, known to be heavily shaped by similar external triggers, to shed light on the process that perturbed the filament where the Class 0 IRAS4 protostars lie. We use new IRAM-NOEMA observations of SiO and CH3OH, both known to trace violent events as shocks, toward IRAS 4A as part of the Large Program Seeds Of Life in Space (SOLIS). We detected three parallel elongated ($>$6000 au) structures, called fingers, with narrow line profiles (~1.5 $km s^{-1}$) peaked at the cloud systemic velocity, tracing gas with high density (5-20 $10^5 cm^{-3}$) and high temperature (80-160 K). They are chemically different, with the northern finger traced by both SiO and CH3OH ([CH3OH]/[SiO]~160-300), while the other two only by SiO ([CH3OH]/[SiO]$$5000 yr, would be consistent with the observations if a substantial fraction of silicon, frozen onto the grain mantles, is released by the shocks.We suggest that the shock train is due to an expanding gas bubble, coming behind NGC 1333 from the southwest and clashing against the filament, where IRAS 4A lies. Finally, we propose a solution to the two-decades long debate on the nature and origin of the widespread narrow SiO emission observed in the south part of NGC 1333, namely that it is due to unresolved trains of shocks., Comment: accepted to MNRAS, stac083

The binding energies (BE) of molecules on the interstellar grains are crucial in the chemical evolution of the interstellar medium (ISM). Both temperature programmed desorption (TPD) laboratory experiments and quantum chemistry computations have often provided, so far, only single values of the BE for each molecule. This is a severe limitation, as the ices enveloping the grain mantles are structurally amorphous, giving rise to a manifold of possible adsorption sites, each with different BEs. However, the ice amorphous nature prevents the knowledge of structural details, hindering the development of a common accepted atomistic icy model. In this work, we propose a computational framework that closely mimics the formation of the interstellar grain mantle through a water by water accretion. On that grain, an unbiased random (but well reproducible) positioning of the studied molecule is then carried out. Here we present the test case of NH$_3$, an ubiquitous species in the molecular ISM. We provide the BE distribution computed by a hierarchy approach, using the semiempirical xTB-GFN2 as low-level method to describe the whole icy cluster combined with the B97D3 DFT functional as high-level method on the local zone of the NH$_3$ interaction. The final ZPE corrected BE is computed at ONIOM(DLPNO-CCSD(T)//B97D3:xTB-GFN2) level, ensuring the best cost/accuracy ratio. The main peak of the predicted NH$_3$ BE distribution is in agreement with experimental TPD and literature computed data. A second broad peak at very low BE values is also present, never detected before. It may provide the solution to a long-standing puzzle about the presence of gaseous NH$_3$ observed also in cold ISM objects.

A solar-type system starts from an initial molecular core that acquires organic complexity as it evolves. The so-called prestellar cores that can be studied are rare, which has hampered our understanding of how organic chemistry sets in and grows. Aims. We selected the best prestellar core targets from the cold core catalogue that represent a diversity in terms of their environment to explore their chemical complexity: 1390 (in the compressed shell of Lambda Ori), 869 (in the MBM12 cloud), and 4149 (in the California nebula). We obtained a spectral survey with the IRAM 30 m telescope in order to explore the molecular complexity of the cores. We carried out a radiative transfer analysis of the detected transitions in order to place some constraints on the physical conditions of the cores and on the molecular column densities. We also used the molecular ions in the survey to estimate the cosmic-ray ionisation rate and the S/H initial elemental abundance using a gas-phase chemical model to reproduce their abundances. We found large differences in the molecular complexity (deuteration, complex organic molecules, sulphur, carbon chains, and ions) and compared their chemical properties with a cold core and two prestellar cores. The chemical diversity we found in the three cores seems to be correlated with their chemical evolution: two of them are prestellar (1390 and 4149), and one is in an earlier stage (869). The influence of the environment is likely limited because cold cores are strongly shielded from their surroundings. The high extinction prevents interstellar UV radiation from penetrating deeply into the cores. Higher spatial resolution observations of the cores are therefore needed to constrain the physical structure of the cores, as well as a larger-scale distribution of molecular ions to understand the influence of the environment on their molecular complexity., 26 pages, 13 figures, accepted in A&A in January 2022

The formation of the interstellar complex organic molecules (iCOMs) is a hot topic in astrochemistry. One of the main paradigms trying to reproduce the observations postulates that iCOMs are formed on the ice mantles covering the interstellar dust grains as a result of radical--radical coupling reactions. We investigate iCOMs formation on the icy surfaces by means of computational quantum mechanical methods. In particular, we study the coupling and direct hydrogen abstraction reactions involving the CH$_3$ + X systems (X = NH$_2$, CH$_3$, HCO, CH$_3$O, CH$_2$OH) and HCO + Y (Y = HCO, CH$_3$O, CH$_2$OH), plus the CH$_2$OH + CH$_2$OH and CH$_3$O + CH$_3$O systems. We computed the activation energy barriers of these reactions as well as the binding energies of all the studied radicals, by means of density functional theory (DFT) calculations on two ice water models, made of 33 and 18 water molecules. Then, we estimated the efficiency of each reaction using the reaction activation, desorption and diffusion energies and derived kinetics with the Eyring equations. We find that radical--radical chemistry on surfaces is not as straightforward as usually assumed. In some cases, direct H abstraction reactions can compete with radical--radical couplings, while in others they may contain large activation energies. Specifically, we found that (i) ethane, methylamine and ethylene glycol are the only possible products of the relevant radical--radical reactions; (ii) glyoxal, methyl formate, glycolaldehyde, formamide, dimethyl ether and ethanol formation is likely in competition with the respective H-abstraction products, and (iii) acetaldehyde and dimethyl peroxide do not seem a likely grain surface products., 46 pages, 15 figures. Accepted for publication in ApJs

Interstellar grains are composed by a rocky core (usually amorphous silicates) covered by an icy mantle, the most abundant molecule being H

Understanding the chemical past of our Sun and how life appeared on Earth is no mean feat. The best strategy we can adopt is to study newborn stars located in an environment similar to the one in which our Sun was born and assess their chemical content. In particular, hot corinos are prime targets since recent studies showed correlations between interstellar Complex Organic Molecules (iCOMs) abundances from hot corinos and comets. The ORion ALMA New GEneration Survey (ORANGES) aims to assess the number of hot corinos in the closest and best analogue to our Sun's birth environment, the OMC-2/3 filament. In this context, we investigated the chemical nature of 19 solar-mass protostars and found that 26\% of our sample sources shows warm methanol emission indicative of hot corinos. Compared to the Perseus low-mass star-forming region, where the PErseus ALMA CHEmistry Survey (PEACHES) detected $\sim 60$\% of hot corinos, the latter seem to be relatively scarce in the OMC-2/3 filament. While this suggests that the chemical nature of protostars in Orion and Perseus is different, improved statistics are needed in order to consolidate this result. If the two regions are truly different, this would indicate that the environment is likely playing a role in shaping the chemical composition of protostars., Comment: 16 pages, 8 figures, Accepted in ApJ

Imai et al., The chemical diversity of low-mass protostellar sources has so far been recognized, and environmental effects are invoked as its origin. In this context, observations of isolated protostellar sources without the influence of nearby objects are of particular importance. Here, we report the chemical and physical structures of the low-mass Class 0 protostellar source IRAS 16544−1604 in the Bok globule CB 68, based on 1.3 mm Atacama Large Millimeter/submillimeter Array observations at a spatial resolution of ∼70 au that were conducted as part of the large program FAUST. Three interstellar saturated complex organic molecules (iCOMs), CH3OH, HCOOCH3, and CH3OCH3, are detected toward the protostar. The rotation temperature and the emitting region size for CH3OH are derived to be 131 ± 11 K and ∼10 au, respectively. The detection of iCOMs in close proximity to the protostar indicates that CB 68 harbors a hot corino. The kinematic structure of the C18O, CH3OH, and OCS lines is explained by an infalling–rotating envelope model, and the protostellar mass and the radius of the centrifugal barrier are estimated to be 0.08–0.30 M⊙ and, This paper makes use of the following ALMA data: ADS/JAO.ALMA#2016.1.01376.S. ALMA is a partnership of ESO (representing its member states), NSF (USA) and NINS (Japan), together with NRC (Canada), NSC and ASIAA (Taiwan), and KASI (Republic of Korea), in cooperation with the Republic of Chile. The Joint ALMA Observatory is operated by ESO, AUI/NRAO and NAOJ. The authors acknowledge financial support from JSPS and MAEE under the Japan–France Integrated Action Program (SAKURA: 25765VC). D.J. is supported by NRC Canada and by an NSERC Discovery Grant. E.B. and G.B. acknowledge funding from the European Research Council under the European Union's Horizon 2020 research and innovation program, for the project "The Dawn of Organic Chemistry," grant agreement No. 741002. G.B. acknowledges support from the PID2020-117710GB-I00 grant funded by MCIN/AEI/10.13039/501100011033 and from the Unit of Excellence María de Maeztu 2020–2023 award to the Institute of Cosmos Sciences (CEX2019-00918-M). I.J.-S. has received partial support from the Spanish State Research Agency (AEI) through project Nos. PID2019-105552RB-C41 and MDM-2017-0737 Unidad de Excelencia "Maria de Maeztu" - Centro de Astrobiologia (CSIC-INTA). This study is supported by grants-in-aid from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (18H05222, 18J11010, 19H05069, 19K14753, and 21K13954).

Ethanol (CH$_3$CH$_2$OH) is a relatively common molecule, often found in star forming regions. Recent studies suggest that it could be a parent molecule of several so-called interstellar complex organic molecules (iCOMs). Yet, the formation route of this species remains debated. In the present work, we study the formation of ethanol through the reaction of CCH with one H$_2$O molecule belonging to the ice, as a test case to investigate the viability of chemical reactions based on a "radical + ice component" scheme as an alternative mechanism for the synthesis of iCOMs, beyond the usual radical-radical coupling. This has been done by means of DFT calculations adopting two clusters of 18 and 33 water molecules as ice models. Results indicate that CH$_3$CH$_2$OH can potentially be formed by this proposed reaction mechanism. The reaction of CCH with H$_2$O on the water ice clusters can be barrierless (thanks to the help of boundary icy water molecules acting as proton transfer assistants) leading to the formation of vinyl alcohol precursors (H$_2$CCOH and CHCHOH). Subsequent hydrogenation of vinyl alcohol yielding ethanol is the only step presenting a low activation energy barrier. We finally discuss the astrophysical implications of these findings., 30 pages, 6 figures Accepted for publication ACS Earth and Space Chemistry

Binding energies (BEs) are one of the most important parameters for astrochemical modeling determining, because they govern whether a species stays in the gas-phase or is frozen on the grain surfaces. It is currently known that, in the denser and colder regions of the interstellar medium, sulphur is severely depleted in the gas phase. It has been suggested that it may be locked into the grain icy mantles. However, which are the main sulphur carriers is still a matter of debate. This work aims at establishing accurate BEs of 17 sulphur-containing species on two validated water ice structural models, the proton-ordered crystalline (010) surface and an amorphous water ice surface. We adopted Density Functional Theory (DFT)-based methods (the hybrid B3LYP-D3(BJ) and the hybrid meta-GGA M06-2X functionals) to predict structures and energetics of the adsorption complexes. London's dispersion interactions are shown to be crucial for an accurate estimate of the BEs due to the presence of the high polarizable sulphur element. While on the crystalline model the adsorption is restricted to a very limited number of binding sites with single valued BEs, on the amorphous model several adsorption structures are predicted, giving a BE distribution for each species. With the exception of few cases, both experimental and other computational data are in agreement with our calculated BE values. A final discussion on how useful the computed BEs are with respect to the snow lines of the same species in protoplanetary disks is provided, Comment: 22 pages, 9 figures, Accepted for publication in The Astrophysical Journal

We present ALMA high-angular resolution ($\sim$ 50 au) observations of the Class I binary system SVS13-A. We report images of SVS13-A in numerous interstellar complex organic molecules: CH$_{\rm 3}$OH, $^{13}$CH$_{\rm 3}$OH, CH$_{\rm 3}$CHO, CH$_{\rm 3}$OCH$_{\rm 3}$, and NH$_{\rm 2}$CHO. Two hot corinos at different velocities are imaged in VLA4A (V$_{sys}$= +7.7 km s$^{-1}$) and VLA4B (V$_{sys}$= +8.5 km s$^{-1}$). From a non-LTE analysis of methanol lines we derive a gas density of 3 $\times$ 10$^8$ cm$^{-3}$, and gas temperatures of 140 K and 170 K for VLA4A and VLA4B, respectively. For the other species the column densities are derived from a LTE analysis. Formamide, which is the only N-bearing species detected in our observations, is more prominent around VLA4A, while dimethyl ether, methanol and acetaldehyde are associated with both VLA4A and VLA4B. We derive in the two hot corinos abundance ratios of $\sim$ 1 for CH$_{\rm 3}$OH, $^{13}$CH$_{\rm 3}$OH, and CH$_{\rm 3}$OCH$_{\rm 3}$, $\sim$ 2 for CH$_{\rm 3}$CHO, and $\sim$ 4 for NH$_{\rm 2}$CHO. The present dataset supports a chemical segregation between the different species inside the binary system. The emerging picture is that of an onion-like structure of the two SVS13-A hot corinos, caused by the different binding energies of the species, also supported by ad hoc quantum chemistry calculations. In addition, the comparison between molecular and dust maps suggests that the interstellar complex organic molecules emission originates from slow shocks produced by accretion streamers impacting the VLA4A and VLA4B disks and enriching the gas-phase component., Comment: 20 pages, 14 figures

Context. Hot corinos are compact regions around solar-mass protostellar objects that are very rich in interstellar Complex Organic Molecules (iCOMs). How the abundance of these molecules is affected by the environmental physical conditions is still an open question. More specifically, addressing this point is key to understand our own chemical origins since the Solar System formed in a large cluster of low- to high-mass stars and was therefore subject to external heating and ultraviolet irradiation which may have shaped the chemistry of its early formation stages. Aims. The goal of this high resolution study is to determine the abundance ratios of iCOMs in HOPS-108, which is a Class 0 protostar and a hot corino candidate located in the nearest Solar System analogue, the protostellar cluster OMC-2 FIR 4, in Orion. We aim to compare the abundance ratios to those found in other hot corinos, which are all located in less crowded environments, in order to understand the impact of environmental conditions on hot corinos’ chemistry. Methods. We observed the OMC-2 FIR 4 proto-cluster using the Band 6 of the Atacama Large (sub-)Millimetre Array in Cycle 4 with an angular resolution of ~0.′′28 (110 au). We determined the abundances and temperature of the species using local thermodynamic equilibrium (LTE) and non-LTE analysis. Results. Our results reveal a rich organic chemistry towards HOPS-108, asserting that it is a hot corino where the following iCOMs are detected: CH3OH, HCOOCH3, CH3OCH3, CH318OH, CH2DOH, CH3COCH3, CH3CHO, CH3CN, 13CH3CN, C2H5CN, and NH2CHO. Remarkably, we find a possible enhancement in the HCOOCH3 abundance with respect to other known hot corinos. Indeed, the [CH3OCH3]/[HCOOCH3] abundance ratio in this source is ~0.2 and, within the uncertainties, it deviates from the known correlation marginally where [CH3OCH3]/[HCOOCH3] ~1. A relatively low [CH2DOH]/[CH3OH] abundance ratio of ~0.02 is also obtained, which is in agreement with that found in another Orion source, HH212, suggesting a higher gas temperature during the early phases of ice mantle formation. Conclusions. The [CH3OCH3]/[HCOOCH3] and [CH2DOH]/[CH3OH] abundance ratios in HOPS-108 might result from different physical conditions in the Orion molecular complex compared to other regions. The former ratio cannot be reproduced with current chemical models, highlighting the importance of improving the chemical networks with theoretical calculations. More hot corinos located in heavily clustered regions such as Orion should be targeted in order to measure these ratios and evaluate whether they are an environmental product or whether HOPS-108 is an exceptional hot corino overall.

Ethanol (CH

Despite the detection of numerous interstellar complex organic molecules (iCOMs) for decades, it is still a matter of debate whether they are synthesized in the gas phase or on the icy surface of interstellar grains. In the past, molecular deuteration has been used to constrain the formation paths of small and abundant hydrogenated interstellar species. More recently, the deuteration degree of formamide, one of the most interesting iCOMs, has also been explained with the hypothesis that it is formed by the gas-phase reaction NH2 + H2CO. In this paper, we aim at using molecular deuteration to constrain the formation of another iCOM, glycolaldehyde, which is an important prebiotic species. More specifically, we have performed dedicated electronic structure and kinetic calculations to establish the glycolaldehyde deuteration degree in relation to that of ethanol, which is its possible parent species according to the suggestion of Skouteris et al. We found that the abundance ratio of the species containing one D atom over the all-protium counterpart depends on the produced D isotopomer and varies from 0.9 to 0.5. These theoretical predictions compare extremely well with the monodeuterated isotopomers of glycolaldehyde and that of ethanol measured toward the solar-like protostar IRAS 16293–2422, supporting the hypothesis that glycolaldehyde could be produced in the gas phase for this source. In addition, the present work confirms that the deuterium fractionation of iCOMs cannot be simply anticipated based on the deuterium fractionation of the parent species but necessitates a specific study, as already shown for the case of formamide.

Positive ions play a fundamental role in the interstellar chemistry, especially in cold environments where chemistry is believed to be mainly ion-driven. However, in contrast with neutral species, most of the cations present in the astrochemical reaction networks are not fully characterized in the astrochemical literature. To fill up this gap, we have carried out new accurate quantum chemical calculations to identify the structures and energies of 262 cations with up to 14 atoms that are postulated to have a role in the interstellar chemistry. Optimised structures and rotational constants were obtained at M06-2X/cc-pVTZ level, while electric dipoles and total electronic energies were computed with CCSD(T)/aug-cc-pVTZ//M06-2X/cc-pVTZ single point energy calculations. The present work complements the study by Woon & Herbst (2009), who characterised the structure and energies of 200 neutral species involved as well in the interstellar chemistry. Taken together, the two datasets can be used to estimate whether a reaction, postulated in present astrochemical reaction networks, is feasible from a thermochemistry point of view and, consequently, to improve the reliability of the present networks used to simulate the interstellar chemistry. We provide an actual example of the potential use of the cations plus neutral datasets. It shows that two reactions, involving Si-bearing ions and present in the widely used reaction networks KIDA and UMIST, cannot occur in cold ISM because endothermic.

The latest developments in astrochemistry have shown how some molecular species can be used as a tool to study the early stages of the solar-type star formation process. Among them, the more relevant species are the interstellar complex organic molecules (iCOMs) and the deuterated molecules. Their analysis give us information on the present and past history of protostellar objects. Among the protostellar evolutionary stages, Class I protostars represent a perfect laboratory in which to study the initial conditions for the planet formation process. Indeed, from a physical point of view, the Class I stage is the bridge between the Class 0 phase, dominated by the accretion process, and the protoplanetary disk phase, when planets form. Despite their importance, few observations of Class I protostars exist and very little is known about their chemical content. In this paper we review the (few) existing observations of iCOMs and deuterated species in Class I protostars. In addition, we present new observations of deuterated cyanoacetylene and thioformaldehyde towards the Class I protostar SVS13-A. These new observations allow us to better understand the physical and chemical structure of SVS13-A and compare the cyanoacetylene and thioformaldehyde deuteration with other sources in different evolutionary phases., 51 pages, 10 figures

Formamide (NH$_2$CHO) has been identified as a potential precursor of a wide variety of organic compounds essential to life, and many biochemical studies propose it likely played a crucial role in the context of the origin of life on our planet. The detection of formamide in comets, which are believed to have --at least partially-- inherited their current chemical composition during the birth of the Solar System, raises the question whether a non-negligible amount of formamide may have been exogenously delivered onto a very young Earth about four billion years ago. A crucial part of the effort to answer this question involves searching for formamide in regions where stars and planets are forming today in our Galaxy, as this can shed light on its formation, survival, and chemical re-processing along the different evolutionary phases leading to a star and planetary system like our own. The present review primarily addresses the chemistry of formamide in the interstellar medium, from the point of view of (i) astronomical observations, (ii) experiments, and (iii) theoretical calculations. While focusing on just one molecule, this review also more generally reflects the importance of joining efforts across multiple scientific disciplines in order to make progress in the highly interdisciplinary science of astrochemistry., Review, 5 figures

Formamide (NH2CHO) is considered an important prebiotic molecule because of its potential to form peptide bonds. It was recently detected in the atmosphere of the HH 212 protostellar disk on the Solar-System scale where planets will form. Here we have mapped it and its potential parent molecules HNCO and H2CO, along with other molecules CH3OH and CH3CHO, in the disk atmosphere, studying its formation mechanism. Interestingly, we find a stratified distribution of these molecules, with the outer emission radius increasing from ~ 24 au for NH2CHO and HNCO, to 36 au for CH3CHO, to 40 au for CH3OH, and then to 48 au for H2CO. More importantly, we find that the increasing order of the outer emission radius of NH2CHO, CH3OH, and H2CO is consistent with the decreasing order of their binding energies, supporting that they are thermally desorbed from the ice mantle on dust grains. We also find that HNCO, which has much lower binding energy than NH2CHO, has almost the same spatial distribution, kinematics, and temperature as NH2CHO, and is thus more likely a daughter species of desorbed NH2CHO. On the other hand, we find that H2CO has a more extended spatial distribution with different kinematics from NH2CHO, thus questioning whether it can be the gas-phase parent molecule of NH2CHO., Comment: 22 pages, 5 figures

To understand the origin of the diversity observed in exoplanetary systems, it is crucial to characterize the early stages of their formation, represented by Solar-type protostars. Likely, the gaseous chemical content of these objects directly depends on the composition of the dust grain mantles formed before the collapse. Directly retrieving the ice mantle composition is challenging, but it can be done indirectly by observing the major components, such as NH3 and CH3OH at cm wavelengths, once they are released into the gas-phase during the warm protostellar stage. We observed several CH3OH and NH3 lines toward three Class 0 protostars in NGC1333 (IRAS 4A1, IRAS 4A2, and IRAS 4B), at high angular resolution (1"; ~300 au) with the VLA interferometer at 24-26 GHz. Using a non-LTE LVG analysis, we derived a similar NH3/CH3OH abundance ratio in the three protostars (, accepted in ApJ Letters

To date, about two dozen low-mass embedded protostars exhibit rich spectra with lines of complex organic molecule (COM). These protostars seem to possess different enrichment in COMs. However, the statistics of COM abundance in low-mass protostars are limited by the scarcity of observations. This study introduces the Perseus ALMA Chemistry Survey (PEACHES), which aims at unbiasedly characterizing the chemistry of COMs toward the embedded (Class 0/I) protostars in the Perseus molecular cloud. Of 50 embedded protostars surveyed, 58% of them have emission from COMs. A 56%, 32%, and 40% of the protostars have CH$_3$OH, CH$_3$OCHO, and N-bearing COMs, respectively. The detectability of COMs depends neither on the averaged continuum brightness temperature, a proxy of the H$_2$ column density, nor on the bolometric luminosity and the bolometric temperature. For the protostars with detected COMs, CH$_3$OH has a tight correlation with CH$_3$CN, spanning more than two orders of magnitude in column densities normalized by the continuum brightness temperature, suggesting a chemical relation between CH$_3$OH and CH$_3$CN and a large chemical diversity in the PEACHES samples at the same time. A similar trend with more scatter is also found between all identified COMs, hinting at a common chemistry for the sources with COMs. The correlation between COMs is insensitive to the protostellar properties, such as the bolometric luminosity and the bolometric temperature. The abundance of larger COMs (CH$_3$OCHO and CH$_3$OCH$_3$) relative to that of smaller COMs (CH$_3$OH and CH$_3$CN) increases with the inferred gas column density, hinting at an efficient production of complex species in denser envelopes., 55 pages, 9 tables, 24 figures. Updated after publication in ApJ. Figure 18 appears as a figure set in ApJ

We have observed the very low-mass Class 0 protostar IRAS 15398−3359 at scales ranging from 50 to 1800 au, as part of the Atacama Large Millimeter/Submillimeter Array Large Program FAUST. We uncover a linear feature, visible in H2CO, SO, and C18O line emission, which extends from the source in a direction almost perpendicular to the known active outflow. Molecular line emission from H2CO, SO, SiO, and CH3OH further reveals an arc-like structure connected to the outer end of the linear feature and separated from the protostar, IRAS 15398−3359, by 1200 au. The arc-like structure is blueshifted with respect to the systemic velocity. A velocity gradient of 1.2 km s−1 over 1200 au along the linear feature seen in the H2CO emission connects the protostar and the arc-like structure kinematically. SO, SiO, and CH3OH are known to trace shocks, and we interpret the arc-like structure as a relic shock region produced by an outflow previously launched by IRAS 15398−3359. The velocity gradient along the linear structure can be explained as relic outflow motion. The origins of the newly observed arc-like structure and extended linear feature are discussed in relation to turbulent motions within the protostellar core and episodic accretion events during the earliest stage of protostellar evolution. The authors thank the anonymous reviewer for invaluable comments. They are also grateful to Hauyu Baobab Liu for useful discussions. This paper makes use of the following ALMA data set: ADS/JAO.ALMA#2018.1.01205.L (PI: Satoshi Yamamoto). ALMA is a partnership of the ESO (representing its member states), the NSF (USA) and NINS (Japan), together with the NRC (Canada) and the NSC and ASIAA (Taiwan), in cooperation with the Republic of Chile. The Joint ALMA Observatory is operated by the ESO, the AUI/NRAO, and the NAOJ. The authors thank to the ALMA staff for their excellent support. This work is supported by the projects PRIN-INAF-MAIN-STREAM 2017 Protoplanetary disks seen through the eyes of new-generation instruments, ARIEL and the astrochemical link between circumstellar disks and planets, and the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programmes: The Dawn of Organic Chemistry (DOC), grant agreement No. 741002, and Astro-Chemistry Origins (ACO), grant No. 811312. The National Radio Astronomy Observatory is a facility of the National Science Foundation operated under cooperative agreement by Associated Universities, Inc. I.J.-S. has received partial support from the Spanish FEDER (project number ESP2017-86582-C4-1-R) and the State Research Agency (AEI; project number PID2019-105552RB-C41). D.J. is supported by NRC Canada and by an NSERC Discovery Grant. This project is also supported by a Grant-in-Aid from Japan Society for the Promotion of Science (KAKENHI: Nos. 18H05222, 19H05069, 19K14753). Yuki Okoda thanks the Advanced Leading Graduate Course for Photon Science (ALPS) and Japan Society for the Promotion of Science (JSPS) for financial support. Peerreview

Interstellar grains are known to be important actors in the formation of interstellar molecules such as H$_2$, water, ammonia, and methanol. It has been suggested that the so-called interstellar complex organic molecules (iCOMs) are also formed on the interstellar grain icy surfaces by the combination of radicals via reactions assumed to have an efficiency equal to unity. In this work, we aim to investigate the robustness or weakness of this assumption by considering the case of acetaldehyde (CH$_3$CHO) as a starting study case. In the literature, it has been postulated that acetaldehyde is formed on the icy surfaces via the combination of HCO and CH$_3$. Here we report new theoretical computations on the efficiency of its formation. To this end, we coupled quantum chemical calculations of the energetics and kinetics of the reaction CH$_3$ + HCO, which can lead to the formation of CH$_3$CHO or CO + CH$_4$. Specifically, we combined reaction kinetics computed with the Rice-Ramsperger-Kassel-Marcus (RRKM) theory (tunneling included) method with diffusion and desorption competitive channels. We provide the results of our computations in the format used by astrochemical models to facilitate their exploitation. Our new computations indicate that the efficiency of acetaldehyde formation on the icy surfaces is a complex function of the temperature and, more importantly, of the assumed diffusion over binding energy ratio $f$ of the CH$_3$ radical. If the ratio $f$ is $\geq$0.4, the efficiency is equal to unity in the range where the reaction can occur, namely between 12 and 30 K. However, if $f$ is smaller, the efficiency dramatically crashes: with $f$=0.3, it is at most 0.01. In addition, the formation of acetaldehyde is always in competition with that of CO + CH$_4$., Comment: 14 pages, 12 figures, 11 tables, accepted in A&A

The isotopic ratio of nitrogen presents a wide range of values in the Solar System and in star forming system whose origin is still unclear. Chemical reactions in the gas phase are one of the possible processes that could modify the $^{14}$N/$^{15}$N ratio. We aim at investigating if and how the passage of a shock wave in the interstellar medium, can affect the relative fraction of nitrogen isotopes. The ideal place for such a study is the L1157 outflow, where several shocked clumps are present. We present the first measurement of the $^{14}$N/$^{15}$N ratio in the two shocked clumps, B1 and B0, of the protostellar outflow L1157, derived from the interferomteric maps of the H$^{13}$CN(1-0) and the HC$^{15}$N(1-0) lines. In B1, we find that the H$^{13}$CN(1-0) and HC$^{15}$N(1-0) emission traces the front of the clump, with averaged column density of $N$(H$^{13}$CN) $\sim$ 7$\times$10$^{12}$ cm$^{-2}$ and $N$(HC$^{15}$N) $\sim$ 2$\times$10$^{12}$ cm$^{-2}$. In this region the ratio H$^{13}$CN(1-0)/HC$^{15}$N(1-0) is quite uniform with an average value of $\sim$ 5$\pm$1. The same average value is also measured in the smaller clump B0e. Assuming the standard $^{12}$C/$^{13}$C = 68, we obtain $^{14}$N/$^{15}$N = 340$\pm$70, similar to those usually found in prestellar cores and protostars. We analysed the prediction of a chemical shock model for several shock conditions and we found that the nitrogen and carbon fractionations do not vary much for the first period after the shock. The observed H$^{13}$CN/HC$^{15}$N can be reproduced by a non-dissociative, C-type shock with parameters in agreement with previous modelling of L1157-B1. Both observations and chemical models indicate that the shock propagation does not affect the nitrogen isotopic ratio that remains similar to that measured in lower temperature gas in prestellar cores and in protostellar envelopes., 7 pages, 6 figures

Context. Recent results in astrochemistry have revealed that some molecules, such as interstellar complex organic species and deuterated species, can serve as valuable tools in the investigation of star-forming regions. Sulphuretted species can also be used to follow the chemical evolution of the early stages of a Sun-like star formation process. Aims. The goal is to obtain a census of S-bearing species using interferometric images towards SVS13-A, a Class I object associated with a hot corino that is rich in interstellar complex organic molecules. Methods. To this end, we used the NGC 1333 SVS13-A data at 3 mm and 1.4 mm obtained with the IRAM-NOEMA interferometer in the framework of the SOLIS (Seeds of Life in Space) Large Program. The line emission of S-bearing species was imaged and analyzed using local thermodynamic equilibrium (LTE) and large velocity gradient (LVG) approaches. Results. We imaged the spatial distribution on ≤300 au scale of the line emission of 32SO, 34SO, C32S, C34S, C33S, OCS, H2C32S, H2C34S, and NS. The low excitation (9 K) 32SO line traces: (i) the low-velocity SVS13-A outflow and (ii) the fast (up to 100 km s−1 away from the systemic velocity) collimated jet driven by the nearby SVS13-B Class 0 object. Conversely, the rest of the lines are confined in the inner SVS13-A region, where complex organics were previously imaged. More specifically, the non-LTE LVG analysis of SO, SO2, and H2CS indicates a hot corino origin (size in the 60–120 au range). Temperatures between 50 K and 300 K, as well as volume densities larger than 105 cm−3 have been derived. The abundances of the sulphuretted are in the following ranges: 0.3–6 × 10−6 (CS), 7 × 10−9–1 × 10−7 (SO), 1–10 × 10−7 (SO2), a few 10−10 (H2CS and OCS), and 10−10–10−9 (NS). The N(NS)/N(NS+) ratio is larger than 10, supporting the assessment that the NS+ ion is mainly formed in the extended envelope. Conclusions. The [H2CS]/[H2CO] ratio, once measured at high-spatial resolutions, increases with time (from Class 0 to Class II objects) by more than one order of magnitude (from ≤10−2 to a few 10−1). This suggests that [S]/[O] changes along the process of Sun-like star formation. Finally, the estimate of the [S]/[H] budget in SVS13-A is 2–17% of the Solar System value (1.8 × 10−5), which is consistent with what was previously measured towards Class 0 objects (1–8%). This finding supports the notion that the enrichment of the sulphuretted species with respect to dark clouds remains constant from the Class 0 to the Class I stages of low-mass star formation. The present findings stress the importance of investigating the chemistry of star-forming regions using large observational surveys as well as sampling regions on the scale of the Solar System.

The Class 0 protostar IRAS 16293$-$2422 Source A is known to be a binary system (A1 and A2) or even a multiple system, which processes a complex outflow structure. We have observed this source in the C$^{34}$S, SO, and OCS lines at 3.1 mm with the Atacama Large Millimeter/submillimeter Array (ALMA). A substructure of this source is traced by our high angular-resolution observation (0\farcs12; 20 au) of the continuum emission. The northwest-southeast (NW-SE) outflow on a 2\arcsec\ scale is detected in the SO ($J_N$ = $2_2$--$1_1$) line. Based on the morphology of the SO distribution, this bipolar outflow structure seems to originate from the protostar A1 and its circumstellar disk, or the circummultiple structure of Source A. The rotation motion of the NW-SE outflow is detected in the SO and OCS emissions. We evaluate the specific angular momentum of the outflowing gas to be $(8.6 - 14.3) \times 10^{-4}$ km s$^{-1}$ pc. If the driving source of this outflow is the protostar A1 and its circumstellar disk, it can be a potential mechanism to extract the specific angular momentum of the disk structure. These results can be a hint for the outflow launching mechanism in this source. Furthermore, they provide us with an important clue to resolve the complicated structure of IRAS 16293$-$2422 Source A., Comment: 48 pages, 8 figs

Molecular hydrogen is the most abundant molecular species in the Universe. While no doubts exist that it is mainly formed on the interstellar dust grain surfaces, many details of this process remain poorly known. In this work, we focus on the fate of the energy released by the H$_2$ formation on the dust icy mantles, how it is partitioned between the substrate and the newly formed H$_2$, a process that has a profound impact on the interstellar medium. We carried out state-of-art \textit{ab-initio} molecular dynamics simulations of H$_2$ formation on periodic crystalline and amorphous ice surface models. Our calculations show that up to two thirds of the energy liberated in the reaction ($\sim$300 kJ/mol $\sim$3.1 eV) is absorbed by the ice in less than 1 ps. The remaining energy ($\sim$140 kJ/mol $\sim$1.5 eV) is kept by the newly born H$_2$. Since it is ten times larger than the H$_2$ binding energy on the ice, the new H$_2$ molecule will eventually be released into the gas-phase. The ice water molecules within $\sim$4 \AA ~from the reaction site acquire enough energy, between 3 and 14 kJ/mol (360--1560 K), to potentially liberate other frozen H$_2$ and, perhaps, frozen CO molecules. If confirmed, the latter process would solve the long standing conundrum of the presence of gaseous CO in molecular clouds. Finally, the vibrational state of the newly formed H$_2$ drops from highly excited states ($\nu = 6$) to low ($\nu \leq 2$) vibrational levels in a timescale of the order of ps., Comment: 13 pages, 7 figures Submitted to ApJ (in press)

Planets form in protoplanetary disks and inherit their chemical composition. It is therefore crucial to understand the disks molecular content. We aim to characterize the distribution and abundance of molecules in the disk of DG Tau. In the context of the ALMA chemical survey of Disk-Outflow sources in Taurus (ALMA-DOT) we analyse ALMA observations of the disk of DG Tau in H2CO 3(1,2)-2(1,1), CS 5-4, and CN 2-1 at ~0.15", i.e. ~18 au at 121 pc. H2CO and CS originate from a disk ring at the edge of the 1.3mm dust continuum, with CS probing an outer disk region with respect to H2CO (peaking at ~70 and ~60 au, respectively). CN originates from an outermost disk/envelope region peaking at ~80 au. H2CO is dominated by disk emission, while CS probes also two streams of material possibly accreting onto the disk with a peak of emission where the stream connects to the disk. The ring- and disk-height- averaged column densities are ~2.4-8.6e13 cm-2 (H2CO), ~1.7-2.5e13 cm-2 (CS), and ~1.9-4.7e13 cm-2 (CN). Unsharp masking reveals a ring of enhanced dust emission at ~40 au, i.e. just outside the CO snowline (~30 au). CS and H2CO emissions are co-spatial suggesting that they are chemically linked. The observed rings of molecular emission at the edge of the 1.3mm continuum may be due to dust opacity effects and/or continnum over-subtraction in the inner disk; as well as to increased UV penetration and/or temperature inversion at the edge of the mm-dust which would cause an enhanced gas-phase formation and desorption of these molecules. Moreover, H2CO and CS originate from outside the ring of enhanced dust emission, which also coincides with a change of the linear polarization at 0.87mm. This suggests that outside the CO snowline there could be a change of the dust properties which would reflect in the increase of the intensity (and change of polarization) of continuum, and of molecular emission., 13 pages, accepted for publication on A&A

A first step towards understanding planetary formation is the characterisation of the structure and evolution of protoplanetary discs. A variety of planetary systems has been discovered in recent years and it likely depends on the early history of their formation. Thus understanding the chemical composition of early solar-like protostars is crucial. To be able to study the lines in detail though, a good knowledge of the dust properties and in particular the optical depth is needed in order to interpreted the lines correctly. In this talk I want to present our results of the class I source Elias29 as part of the FAUST (fifty au study of the chemistry in the disk/envelope system of solar-like protostars) collaboration. The goal of FAUST is to quantify the chemical composition of the envelope/disk system of solar-lie class 0 and I protostars. With the high spatial resolution of 50 au in band 3 and band 6 ALMA data we can spatially resolve the envelope and the disk on this source and calculate the dust properties of the two components.