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R. T. Garrod

Publications and source records attributed to R. T. Garrod.

At least 37 records · Page 2Linked to original sources

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$^{-2}$.

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Exploring molecular complexity with ALMA (EMoCA): Complex isocyanides in Sgr B2(N)

We used the EMoCA survey data to search for isocyanides in Sgr B2(N2) and their corresponding cyanide analogs. We then used the coupled three-phase chemical kinetics code MAGICKAL to simulate their chemistry. Several new species, and over 100 new reactions have been added to the network. In addition, a new single-stage simultaneous collapse/warm-up model has been implemented, thus eliminating the need for the previous two-stage models. A variable, visual extinction-dependent $ζ$ was also incorporated into the model and tested. We report the tentative detection of CH$_3$NC and HCCNC in Sgr B2(N2), which represents the first detection of both species in a hot core of Sgr B2. Our updated chemical models can reproduce most observed NC:CN ratios reasonably well depending on the physical parameters chosen. The model that performs best has an extinction-dependent cosmic-ray ionization rate that varies from ~2 $\times$ 10$^{-15}$ s$^{-1}$ at the edge of the cloud to ~1 $\times$ 10$^{-16}$ s$^{-1}$ in the center. Models with higher extinction-dependent $ζ$ than this model generally do not agree as well, nor do models with a constant $ζ$ greater than the canonical value of 1.3 $\times$ 10$^{-17}$ s$^{-1}$ throughout the source. Radiative transfer models are run using results of the best-fit chemical model. Column densities produced by the radiative transfer models are significantly lower than those determined observationally. Inaccuracy in the observationally determined density and temperature profiles is a possible explanation. Excitation temperatures are well reproduced for the true ``hot core'' molecules, but are more variable for other molecules such as HC$_3$N, for which fewer lines exist in ALMA Band 3.

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Rotational spectrum of isotopic methyl mercaptan, (13)CH3SH, in the laboratory and towards Sagittarius B2(N2)

Methyl mercaptan (CH3SH) is a known interstellar molecule with abundances high enough that the detection of some of its minor isotopologues is promising. The present study aims at providing accurate spectroscopic parameters for the (13)CH3SH isotopologue to facilitate its identification in the interstellar medium at millimetre and submillimetre wavelengths. Through careful analysis of recent CH3SH spectra from 49-510 GHz and 1.1-1.5 THz recorded at natural isotopic composition, extensive assignments were possible not only for the ground torsional state of (13)CH3SH, but also in the first and second excited states. The torsion-rotation spectrum displays complex structure due to the large-amplitude internal rotation of the (13)CH3 group, similar to the main and other minor isotopic species of methyl mercaptan. The assigned transition frequencies have been fitted to within experimental error with a 52-parameter model employing the RAM36 programme. With predictions based on this fit, (13)CH3SH was searched for in spectra from the Atacama Large Millimetre/submillimetre Array (ALMA) towards the Galactic centre source Sgr B2(N2). Several transitions were expected to be observable, but all of them turned out to be severely blended with emission from other species, which prevents us from identifying (13)CH3SH in this source.

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The ALMA-PILS survey: propyne (CH$_3$CCH) in IRAS 16293$-$2422

Context. Propyne (CH$_3$CCH) has been detected in a variety of environments, from Galactic star-forming regions to extragalactic sources. Such molecules are excellent tracers of the physical conditions in star-forming regions. Aims. This study explores the emission of CH$_3$CCH in the low-mass protostellar binary, IRAS 16293$-$2422, examining the spatial scales traced by this molecule, as well as its formation and destruction pathways. Methods. ALMA observations from the Protostellar Interferometric Line Survey (PILS) are used to determine the abundances and excitation temperatures of CH$_3$CCH towards both protostars, exploring spatial scales from 70 to 2400 au. The three-phase chemical kinetics model MAGICKAL is also used, to explore the chemical reactions of this molecule. Results. CH$_3$CCH is detected towards both IRAS 16293A and IRAS 16293B and is found to trace the hot corino component around each source in the PILS dataset. Eighteen transitions above 3$σ$ are detected, enabling robust excitation temperatures and column densities to be determined in each source. In IRAS 16293A, an excitation temperature of 90 K and a column density of 7.8$\times$10$^{15}$ cm$^{-2}$ best fits the spectra. In IRAS 16293B, an excitation temperature of 100 K and 6.8$\times$10$^{15}$ cm$^{-2}$ best fits the spectra. The chemical modelling finds that in order to reproduce the observed abundances, both gas-phase and grain-surface reactions are needed. Conclusions. CH$_3$CCH is a molecule whose brightness and abundance in many different regions can be utilised to provide a benchmark of molecular variation with the physical properties of star-forming regions. It is essential when making such comparisons, that the abundances are determined with a good understanding of the spatial scale of the emitting region, to ensure that accurate abundances are derived.

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Re-exploring Molecular Complexity with ALMA (ReMoCA): Interstellar detection of urea

Urea, NH2C(O)NH2, is a molecule of great importance in organic chemistry and biology. Two searches for urea in the interstellar medium were reported in the past, but neither were conclusive. We want to take advantage of the increased sensitivity and angular resolution provided by ALMA to search for urea toward the hot cores embedded in the high-mass star forming region Sgr B2(N). We use the new spectral line survey ReMoCA performed toward Sgr B2(N) with ALMA in its observing cycle 4. The spectra are analyzed under the LTE approximation. We construct a full synthetic spectrum that includes all the molecules identified so far. We use new spectroscopic predictions for urea in its vibrational ground state and first vibrationally excited state to search for this complex organic molecule in the ReMoCA data set. We employ the gas-grain chemical kinetics model MAGICKAL to interpret the astronomical observations. We report the secure detection of urea toward the hot core Sgr B2(N1) at a position called N1S slightly offset from the continuum peak, which avoids obscuration by the dust.. We derive a column density of 2.7x10^16 cm-2 for urea, two orders of magnitude lower than formamide, and one order of magnitude below methyl isocyanate, acetamide, and N-methylformamide. The latter molecule is reliably identified toward N1S with 60 clearly detected lines, confirming an earlier claim of its tentative interstellar detection. We report the first interstellar detections of NH2CH18O and 15NH2CHO. We also report the nondetection of urea toward the secondary hot core Sgr B2(N2) with an abundance relative to the other four species at least one order of magnitude lower than toward the main hot core. Our chemical model roughly reproduces the relative abundances of formamide, methyl isocyanate, acetamide, and N-methylformamide, but it overproduces urea by at least one order of magnitude.

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The complex chemistry of hot cores in Sagittarius B2(N): Influence of cosmic-ray ionization and thermal history

As the number of complex organic molecules (COMs) detected in the interstellar medium increases, it becomes important to place meaningful constraints on the formation pathways of these species. The molecular cloud SgrB2(N) is host to several hot molecular cores in the early stage of star formation, where a great variety of COMs are detected in the gas phase. Because of its exposure to the extreme conditions of the the Galactic center region, SgrB2(N) is one of the best targets to study the impact of environmental conditions on the production of COMs. Our main goal is to characterize the physico-chemical evolution of SgrB2(N)'s sources in order to explain their chemical differences and constrain their environmental conditions. The chemical composition of SgrB2(N)'s hot cores, N2, N3, N4, and N5 is derived by modeling their 3mm emission spectra extracted from the EMoCA imaging spectral line survey performed with ALMA. We derive the density distribution in the envelope of the sources based on the masses computed from the ALMA dust continuum emission maps. We use the radiative transfer code RADMC-3D to compute temperature profiles based on the COM rotational temperatures derived from population diagrams. We use published results of 3D RMHD simulations of high-mass star formation to estimate the time evolution of the sources properties. We employ the chemical code MAGICKAL to compute time-dependent chemical abundances in the sources and investigate how physical properties and environmental conditions influence the production of COMs. We find that chemical models with a cosmic-ray ionization rate of 7e-16s-1 best reproduce the abundances with respect to methanol of ten COMs observed toward SgrB2(N2-N5). We also show that COMs still form efficiently on dust grains with minimum dust temperatures in the prestellar phase as high as 15K, but that minimum temperatures higher than 25K are excluded.

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Small-scale physical and chemical structure of diffuse and translucent molecular clouds along the line of sight to Sgr B2

The diffuse and translucent molecular clouds traced in absorption along the line of sight to strong background sources have so far been investigated mainly in the spectral domain because of limited angular resolution or small sizes of the background sources. We aim to resolve and investigate the spatial structure of molecular clouds traced by several molecules detected in absorption along the line of sight to SgrB2(N). We have used spectral line data from the EMoCA survey performed with ALMA, taking advantage of the high sensitivity and angular resolution. We identify, on the basis of the spectral analysis of c-C3H2 across the field of view, 15 main velocity components along the line of sight to SgrB2(N) and several components in the envelope of SgrB2. The c-C3H2 column densities reveal two categories of clouds. Clouds in Category I (3 kpc arm, 4 kpc arm, and some GC clouds) have smaller c-C3H2 column densities, smaller linewidths, and smaller widths of their column density PDFs than clouds in Category II (Scutum arm, Sgr arm, and other GC clouds). To investigate the spatial structure we derive opacity maps for the following molecules: c-C3H2, H13CO+, 13CO, HNC, HN13C, HC15N, CS, C34S, 13CS, SiO, SO, and CH3OH. These maps reveal that most molecules trace relatively homogeneous structures that are more extended than the field of view defined by the background continuum emission (about 15", that is 0.08-0.6pc depending on the distance). SO and SiO show more complex structures with smaller clumps of size ~5-8". Our analysis suggests that the driving of the turbulence is mainly solenoidal in the investigated clouds. On the basis of HCO+, we conclude that most line-of-sight clouds towards SgrB2 are translucent, including all clouds where complex organic molecules were recently detected. We also conclude that CCH and CH are good probes of H2 in both diffuse and translucent clouds.

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The ALMA-PILS survey: first detection of methyl isocyanide (CH$_3$NC) in a solar-type protostar

Methyl isocyanide (CH$_3$NC) is the isocyanide with the largest number of atoms confirmed in the interstellar medium (ISM), but it is not an abundant molecule, having only been detected towards a handful of objects. Conversely, its isomer, methyl cyanide (CH$_3$CN), is one of the most abundant complex organic molecules detected in the ISM, with detections in a variety of low- and high-mass sources. We use ALMA observations from the Protostellar Interferometric Line Survey (PILS) to search for methyl isocyanide and compare its abundance with that of its isomer methyl cyanide. We use a new line catalogue from the Cologne Database for Molecular Spectroscopy (CDMS) to identify methyl isocyanide lines. We also model the chemistry with an updated version of the three-phase chemical kinetics model {\em MAGICKAL}, presenting the first chemical modelling of methyl isocyanide to date. We detect methyl isocyanide for the first time in a solar-type protostar, IRAS 16293$-$2422 B, and present upper limits for its companion protostar, IRAS 16293$-$2422 A. Methyl isocyanide is found to be at least 20 times more abundant in source B compared to source A, with a CH$_3$CN/CH$_3$NC abundance ratio of 200 in IRAS 16293--2422 B and >5517 in IRAS 16293$-$2422 A. We also present the results of a chemical model of methyl isocyanide chemistry in both sources, and discuss the implications on methyl isocyanide formation mechanisms and the relative evolutionary stages of both sources.

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The ALMA-PILS survey: Complex nitriles towards IRAS 16293--2422

Complex organic molecules are readily detected in the inner regions of the gaseous envelopes of forming protostars. In particular, molecules that contain nitrogen are interesting due to the role nitrogen plays in the development of life and the compact scales such molecules have been found to trace around forming protostars. The goal of this work is to determine the inventory of one family of nitrogen-bearing organic molecules, complex nitriles (molecules with a $-$CN functional group) towards two hot corino sources in the low-mass protostellar binary IRAS 16293$-$2422. This work explores the abundance differences between the two sources, the isotopic ratios, and the spatial extent derived from molecules containing the nitrile functional group. Using data from the Protostellar Interferometric Line Survey (PILS) obtained with ALMA we determine abundances and excitation temperatures for the detected nitriles. We also present a new method for determining the spatial structure of sources with high line density and large velocity gradients $-$ Velocity-corrected INtegrated emission (VINE) maps. We detect methyl cyanide (CH$_3$CN) as well as 5 of its isotopologues, including the detection of CHD$_2$CN which is the first detection in the ISM. We also detect ethyl cyanide (C$_2$H$_5$CN), vinyl cyanide (C$_2$H$_3$CN), and cyanoacetylene (HC$_3$N). We find that abundances are similar between IRAS 16293A and IRAS 16293B on small scales except for vinyl cyanide which is only detected towards the latter source. This suggests an important difference between the sources either in their evolutionary stage or warm-up timescales. We also detect a spatially double-peaked emission for the first time in molecular emission in the A source, suggesting that this source is showing structure related to a rotating toroid of material.

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Modeling CO, CO$_2$ and H$_2$O ice abundances in the envelopes of young stellar objects in the Magellanic Clouds

Massive young stellar objects in the Magellanic Clouds show infrared absorption features corresponding to significant abundances of CO, CO$_2$ and H$_2$O ice along the line of sight, with the relative abundances of these ices differing between the Magellanic Clouds and the Milky Way. CO ice is not detected towards sources in the Small Magellanic Cloud, and upper limits put its relative abundance well below sources in the Large Magellanic Cloud and the Milky Way. We use our gas-grain chemical code MAGICKAL, with multiple grain sizes and grain temperatures, and further expand it with a treatment for increased interstellar radiation field intensity to model the elevated dust temperatures observed in the MCs. We also adjust the elemental abundances used in the chemical models, guided by observations of HII regions in these metal-poor satellite galaxies. With a grid of models, we are able to reproduce the relative ice fractions observed in MC massive young stellar objects (MYSOs), indicating that metal depletion and elevated grain temperature are important drivers of the MYSO envelope ice composition. Magellanic Cloud elemental abundances have a sub-galactic C/O ratio, increasing H$_2$O ice abundances relative to the other ices; elevated grain temperatures favor CO$_2$ production over H$_2$O and CO. The observed shortfall in CO in the Small Magellanic Cloud can be explained by a combination of reduced carbon abundance and increased grain temperatures. The models indicate that a large variation in radiation field strength is required to match the range of observed LMC abundances. CH$_3$OH abundance is found to be enhanced in low-metallicity models, providing seed material for complex organic molecule formation in the Magellanic Clouds.

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First detection of cyanamide (NH$_2$CN) towards solar-type protostars

Searches for the prebiotically-relevant cyanamide (NH$_2$CN) towards solar-type protostars have not been reported in the literature. We here present the first detection of this species in the warm gas surrounding two solar-type protostars, using data from the Atacama Large Millimeter/Submillimeter Array Protostellar Interferometric Line Survey (PILS) of IRAS 16293-2422 B and observations from the IRAM Plateau de Bure Interferometer of NGC1333 IRAS2A. We furthermore detect the deuterated and $^{13}$C isotopologues of NH$_2$CN towards IRAS 16293-2422 B. This is the first detection of NHDCN in the interstellar medium. Based on a local thermodynamic equilibrium analysis, we find that the deuteration of cyanamide ($\sim$ 1.7%) is similar to that of formamide (NH$_2$CHO), which may suggest that these two molecules share NH$_2$ as a common precursor. The NH$_2$CN/NH$_2$CHO abundance ratio is about 0.2 for IRAS 16293-2422 B and 0.02 for IRAS2A, which is comparable to the range of values found for Sgr B2. We explored the possible formation of NH$_2$CN on grains through the NH$_2$ + CN reaction using the chemical model MAGICKAL. Grain-surface chemistry appears capable of reproducing the gas-phase abundance of NH$_2$CN with the correct choice of physical parameters.

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Complex organic molecules in diffuse clouds along the line of sight to Sgr B2

Up to now, mostly relatively simple molecules have been detected in interstellar diffuse molecular clouds in our galaxy, but more complex species have been reported in the diffuse/translucent medium of a z = 0.89 spiral galaxy. We aim at searching for complex organic molecules (COMs) in diffuse molecular clouds along the line of sight to Sgr B2(N), taking advantage of the high sensitivity and angular resolution of the Atacama Large Millimeter/submillimeter Array (ALMA). We use data acquired as part of the EMoCA survey performed with ALMA. To analyse the absorption features of the molecules detected towards the ultracompact HII region K4 in Sgr B2(N), we calculate synthetic spectra for these molecules and fit their column densities, line widths, centroid velocities, and excitation temperatures. We report the detection of CH3OH, CH3CN, CH3CHO, HC3N, and NH2CHO in Galactic center (GC) diffuse clouds and CH3OH and CH3CN in a diffuse cloud in the Scutum arm. The chemical composition of one of the diffuse GC clouds is found to be similar to the one of the diffuse/translucent medium of the z=0.89 spiral galaxy. The chemical processes leading to chemical complexity in the diffuse molecular ISM appear to have remained similar since z=0.89. As proposed in previous studies, the presence of COMs in diffuse molecular clouds may result from a cyclical interstellar process of cloud contraction and expansion between diffuse and dense states.

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The ALMA-PILS survey: Detection of CH$_{3}$NCO toward the low-mass protostar IRAS 16293-2422 and laboratory constraints on its formation

Methyl isocyanate (CH$_{3}$NCO) belongs to a select group of interstellar molecules considered to be relevant precursors in the formation of larger organic compounds, including those with peptide bonds. The molecule has only been detected in a couple of high-mass protostars and potentially on comets. A formation route on icy grains has been postulated for this molecule but experimental evidence is lacking. Here we extend the range of environments where methyl isocyanate is found, and unambiguously identify CH$_{3}$NCO through the detection of 43 unblended transitions in the ALMA Protostellar Interferometric Line Survey (PILS) of the low mass solar-type protostellar binary IRAS 16293-2422. The molecule is detected toward both components of the binary with a ratio HNCO/CH$_3$NCO $\sim$4--12. The isomers CH$_{3}$CNO and CH$_3$OCN are not identified, resulting in upper abundance ratios of CH$_{3}$NCO/CH$_{3}$CNO > 100 and CH$_{3}$NCO/CH$_3$OCN > 10. The resulting abundance ratios compare well with those found for related N-containing species toward high-mass protostars. To constrain its formation, a set of cryogenic UHV experiments is performed. VUV irradiation of CH$_{4}$:HNCO mixtures at 20 K strongly indicate that methyl isocyanate can be formed in the solid-state through CH$_{3}$ and (H)NCO recombinations. Combined with gas-grain models that include this reaction, the solid-state route is found to be a plausible scenario to explain the methyl isocyanate abundances found in IRAS 16293-2422.

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Exploring molecular complexity with ALMA (EMoCA): Detection of three new hot cores in Sagittarius B2(N)

The SgrB2 molecular cloud contains several sites forming high-mass stars. SgrB2(N) is one of its main centers of activity. It hosts several compact and UCHII regions, as well as two known hot molecular cores (SgrB2(N1) and SgrB2(N2)), where complex organic molecules are detected. Our goal is to use the high sensitivity of ALMA to characterize the hot core population in SgrB2(N) and shed a new light on the star formation process. We use a complete 3 mm spectral line survey conducted with ALMA to search for faint hot cores in SgrB2(N). We report the discovery of three new hot cores that we call SgrB2(N3), SgrB2(N4), and SgrB2(N5). The three sources are associated with class II methanol masers, well known tracers of high-mass star formation, and SgrB2(N5) also with a UCHII region. The chemical composition of the sources and the column densities are derived by modelling the whole spectra under the assumption of LTE. The H2 column densities are computed from ALMA and SMA continuum emission maps. The H2 column densities of these new hot cores are found to be 16 up to 36 times lower than the one of the main hot core Sgr B2(N1). Their spectra have spectral line densities of 11 up to 31 emission lines per GHz, assigned to 22-25 molecules. We derive rotational temperatures around 140-180 K for the three new hot cores and mean source sizes of 0.4 for SgrB2(N3) and 1.0 for SgrB2(N4) and SgrB2(N5). SgrB2(N3) and SgrB2(N5) show high velocity wing emission in typical outflow tracers, with a bipolar morphology in their integrated intensity maps suggesting the presence of an outflow, like in SgrB2(N1). The associations of the hot cores with class II methanol masers, outflows, and/or UCHII regions tentatively suggest the following age sequence: SgrB2(N4), SgrB2(N3), SgrB2(N5), SgrB2(N1). The status of SgrB2(N2) is unclear. It may contain two distinct sources, a UCHII region and a very young hot core.

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Exploring molecular complexity with ALMA (EMoCA): Simulations of branched carbon-chain chemistry in Sgr B2(N)

Using mm-wavelength data from ALMA, the EMoCA spectral line survey revealed the presence of both the straight-chain and branched forms of propyl cyanide (C$_3$H$_7$CN) toward the Galactic Center star-forming source Sgr B2(N2). This was the first interstellar detection of a branched aliphatic molecule. Through computational methods, we seek to explain the observed $i$:$n$ ratio for propyl cyanide, and to predict the abundances of the four different forms of the homologous nitrile, butyl cyanide (C$_4$H$_9$CN). We also investigate whether other molecules will show a similar degree of branching, by modeling alkanes up to pentane (C$_5$H$_{12}$). We use a coupled three-phase chemical kinetics model to simulate the chemistry of Sgr B2(N2), using an updated chemical network that includes grain-surface/ice-mantle formation routes for branched nitriles and alkanes. We use the EMoCA survey data to search for the straight-chain form of butyl cyanide toward Sgr B2(N2). The observed $i$:$n$ ratio for propyl cyanide is reproduced by the models. Butyl cyanide is predicted to show similar abundances to propyl cyanide, and to exhibit strong branching, with the $sec$ form clearly dominant over all others. The addition of CN to acetylene and ethene is found to be important to the production of vinyl, ethyl, propyl, and butyl cyanide. We report a non-detection of $n$-C$_4$H$_9$CN toward Sgr B2(N2), with an abundance at least 1.7 times lower than that of $n$-C$_3$H$_7$CN. This value is within the range predicted by the chemical models. The models indicate that the degree of branching rises with increasing molecular size. The efficiency of CN addition to unsaturated hydrocarbons boosts the abundances of nitriles in the model, and enhances the ratio of straight-to-branched molecule production. The predicted abundance of $s$-C$_4$H$_9$CN makes it a good candidate for future detection toward Sgr B2(N2).

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Rotational spectroscopy, tentative interstellar detection, and chemical modelling of N-methylformamide

N-methylformamide, CH3NHCHO, may be an important molecule for interstellar pre-biotic chemistry because it contains a peptide bond. The rotational spectrum of the most stable trans conformer of CH3NHCHO is complicated by strong torsion-rotation interaction due to the low barrier of the methyl torsion. We use two absorption spectrometers in Kharkiv and Lille to measure the rotational spectra over 45--630 GHz. The analysis is carried out using the Rho-axis method and the RAM36 code. We search for N-methylformamide toward the hot molecular core Sgr B2(N2) using a spectral line survey carried out with ALMA. The astronomical results are put into a broader astrochemical context with the help of a gas-grain chemical kinetics model. The laboratory data set for the trans conformer of CH3NHCHO consists of 9469 line frequencies with J <= 62, including the first assignment of the rotational spectra of the first and second excited torsional states. All these lines are fitted within experimental accuracy. We report the tentative detection of CH3NHCHO towards Sgr B2(N2). We find CH3NHCHO to be more than one order of magnitude less abundant than NH2CHO, a factor of two less abundant than CH3NCO, but only slightly less abundant than CH3CONH2. The chemical models indicate that the efficient formation of HNCO via NH + CO on grains is a necessary step in the achievement of the observed gas-phase abundance of CH3NCO. Production of CH3NHCHO may plausibly occur on grains either through the direct addition of functional-group radicals or through the hydrogenation of CH3NCO. Provided the detection of CH3NHCHO is confirmed, the only slight underabundance of this molecule compared to its more stable structural isomer acetamide and the sensitivity of the model abundances to the chemical kinetics parameters suggest that the formation of these two molecules is controlled by kinetics rather than thermal equilibrium.

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The ALMA-PILS survey: First detections of ethylene oxide, acetone and propanal toward the low-mass protostar IRAS 16293-2422

One of the open questions in astrochemistry is how complex organic and prebiotic molecules are formed. Aims. Our aim is to start the process of compiling an inventory of oxygen-bearing complex organic molecules toward the solar-type Class 0 protostellar binary IRAS16293-2422 from an unbiased spectral survey with ALMA (PILS). Here we focus on the new detections of ethylene oxide (c-C$_2$H$_4$O), acetone (CH$_3$COCH$_3$), and propanal (C$_2$H$_5$CHO). Methods. With ALMA, we surveyed the spectral range from 329 to 363 GHz at 0.5$"$ (60 AU diameter) resolution. Using a simple model for the molecular emission in LTE, the excitation temperatures and column densities of each species were constrained. Results. We successfully detect propanal (44 lines), ethylene oxide (20 lines) and acetone (186 lines) toward one component of the protostellar binary, IRAS16293B. The high resolution maps demonstrate that the emission for all investigated species originates from the compact central region close to the protostar. This, along with a derived common excitation temperature of $\sim$ 125 K, is consistent with a coexistence of these molecules in the same gas. Conclusions. The observations mark the first detections of acetone, propanal and ethylene oxide toward a low-mass protostar. The relative abundance ratios of the two sets of isomers (CH$_3$COCH$_3$/C$_2$H$_5$CHO $\sim$ 8 and CH$_3$CHO/c-C$_2$H$_4$O $\sim$ 12) are comparable to previous observations toward high-mass protostars. The majority of observed abundance ratios from these results as well as those measured toward high-mass protostars are up to an order of magnitude above the predictions from chemical models. This may reflect either missing reactions or uncertain rates in the chemical networks. The physical conditions, such as temperatures or densities, used in the models, may not be applicable to solar-type protostars either.

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The ALMA Protostellar Interferometric Line Survey (PILS): First results from an unbiased submillimeter wavelength line survey of the Class 0 protostellar binary IRAS 16293-2422 with ALMA

The inner regions of the envelopes surrounding young protostars are characterised by a complex chemistry, with prebiotic molecules present on the scales where protoplanetary disks eventually may form. This paper introduces a systematic survey, "Protostellar Interferometric Line Survey (PILS)" of the Class 0 protostellar binary IRAS 16293-2422 using the Atacama Large Millimeter/submillimeter Array (ALMA). The survey covers the full frequency range from 329 to 363 GHz (0.8 mm) with additional targeted observations at 3.0 and 1.3 mm. More than 10,000 features are detected toward one component in the protostellar binary. Glycolaldehyde, its isomers, methyl formate and acetic acid, and its reduced alcohol, ethylene glycol, are clearly detected. For ethylene glycol both lowest state conformers, aGg' and gGg', are detected, the latter for the first time in the ISM. The abundance of glycolaldehyde is comparable to or slightly larger than that of ethylene glycol. In comparison to the Galactic Center, these two species are over-abundant relative to methanol, possibly an indication of formation at low temperatures in CO-rich ices. Both 13C and deuterated isotopologues of glycolaldehyde are detected, also for the first time ever in the ISM. For the deuterated species, a D/H ratio of approximately 5% is found with no differences between the deuteration in the different functional groups of glycolaldehyde. Measurements of the 13C-species lead to a 12C:13C ratio of approximately 30, lower than the typical ISM value. This low ratio may reflect an enhancement of 13CO in the ice due to either ion-molecule reactions in the gas before freeze-out or differences in the temperatures where 12CO and 13CO ices sublimate. The results reinforce the importance of low-temperature grain surface chemistry for the formation of prebiotic molecules seen here in the gas after sublimation of the entire ice mantle.

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