arXiv subjects

L. Colzi

Publications and source records attributed to L. Colzi.

At least 55 records · Page 3Linked to original sources

arXiv2022

CHEMOUT: CHEMical complexity in star-forming regions of the OUTer Galaxy. I. Organic molecules and tracers of star-formation activity

The outer Galaxy is an environment with metallicity lower than the Solar one. Because of this, the formation and survival of molecules in star-forming regions located in the inner and outer Galaxy is expected to be different. To gain understanding on how chemistry changes throughout the Milky Way, it is crucial to observe outer Galaxy star-forming regions to constrain models adapted for lower metallicity environments. In this paper we present a new observational project: chemical complexity in star-forming regions of the outer Galaxy (CHEMOUT). The goal is to unveil the chemical composition in 35 dense molecular clouds associated with star-forming regions of the outer Galaxy through observations obtained with the IRAM 30m telescope. In this first paper, we present the sample, and report the detection at 3~mm of simple organic species HCO+, H13CO+, HCN, c-C3H2, HCO, C4H, and HCS+, of the complex hydrocarbon CH3CCH, and of SiO, CCS and SO. From c-C3H2, we estimate new kinematic heliocentric and Galactocentric distances based on an updated rotation curve of the Galaxy. The detection of the molecular tracers does not seem to have a clear dependence on the Galactocentric distance. We also analyse the HCO+ line profiles. We find high velocity wings in ~71% of the targets, and their occurrence does not depend on the Galactocentric distance. Our results, confirmed by a statistical analysis, show that the presence of organic molecules and tracers of protostellar activity is ubiquitous in the low-metallicity environment of the outer Galaxy. Based on this, and on the additional evidence that small, terrestrial planets are omnipresent in the Galaxy, we support previous claims that the definition of Galactic Habitable Zone should be rediscussed in view of the ubiquitous capacity of the interstellar medium to form organic molecules.

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arXiv2022

Deuterium fractionation as a multi-phase component tracer in the Galactic Centre

The Central Molecular Zone (CMZ) contains most of the mass of our Galaxy but its star formation rate is one order of magnitude lower than in the Galactic disc. This is likely related to the fact that the bulk of the gas in the CMZ is in a warm ($>$100 K) and turbulent phase with little material in the pre-stellar phase. We present in this Letter observations of deuterium fractionation (D/H ratios) of HCN, HNC, HCO$^{+}$, and N$_{2}$H$^{+}$ towards the CMZ molecular cloud G+0.693-0.027. These observations clearly show, for the first time, the presence of a colder, denser, and less turbulent narrow component, with a line width of $\sim$9 km s$^{-1}$, in addition to the warm, less dense and turbulent broad component with a line width of $\sim$20 km s$^{-1}$. The very low D/H ratio $\le$6$\times$10$^{-5}$ for HCO$^{+}$ and N$_{2}$H$^{+}$, close to the cosmic value ($\sim$2.5$\times$10$^{-5}$), and the high D/H ratios $>$4$\times$10$^{-4}$ for HCN and HNC derived for the broad component, confirm the presence of high-temperatures deuteration routes for nitriles. For the narrow component we have derived D/H ratios $>$10$^{-4}$ and excitation temperatures of $7$ K for all molecules, suggesting kinetic temperatures $\le$30 K and H$_2$ densities $\ge$5$\times$10$^{4}$ cm$^{-3}$, at least one order of magnitude larger than for the broad component. The method presented in this Letter allows to identify clouds on the verge of star formation, i.e. under pre-stellar conditions, towards the CMZ. This method can also be used for the identification of such clouds in external galaxies.

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arXiv2022

First extragalactic detection of a phosphorus-bearing molecule with ALCHEMI: phosphorus nitride (PN)

Phosphorus (P) is a crucial element for life given its central role in several biomolecules. P-bearing molecules have been discovered in different regions of the Milky Way, but not yet towards an extragalactic environment. We have searched for P-bearing molecules towards the nearby starburst Galaxy NGC 253. Using observations from the ALMA Comprehensive High-resolution Extragalactic Molecular Inventory (ALCHEMI) project, we used the MADCUBA package to model the emission of P-bearing molecules assuming Local Thermodynamic Equilibrium (LTE) conditions. We have also performed a non-LTE analysis using SpectralRadex. We report the detection of a P-bearing molecule, phosphorus nitride (PN), for the first time in an extragalactic environment, towards two giant molecular clouds (GMCs) of NGC 253. The LTE analysis yields total PN beam-averaged column densities $N$=(1.20$\pm$0.09)$\times$10$^{13}$ cm$^{-2}$ and $N$=(6.5$\pm$1.6)$\times$10$^{12}$ cm$^{-2}$, which translate into abundances with respect to H$_2$ of $χ$=(8.0$\pm$1.0)$\times$10$^{-12}$ and $χ$=(4.4$\pm$1.2)$\times$10$^{-12}$. We derived a low excitation temperature of $T_{\rm ex}$=(4.4$\pm$1.3) K towards the GMC with the brightest PN emission, which indicates that PN is sub-thermally excited. The non-LTE analysis results in column densities consistent with the LTE values. We have also searched for other P-bearing molecules (PO, PH$_{3}$, CP and CCP), and upper limits were derived. The derived PO/PN ratios are $<$1.3 and $<$1.7. The abundance ratio between PN and the shock-tracer SiO derived towards NGC 253 follows the same trend previously found towards Galactic sources. Comparison of the observations with chemical models indicates that the derived molecular abundances of PN in NGC 253 can be explained by shock-driven chemistry followed by cosmic-ray-driven photochemistry.

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arXiv2021

The trans/cis ratio of formic, HCOOH, and thioformic, HC(O)SH, acids in the Interstellar Medium

We studied theoretically the cis-trans isomerization reactions of two astrophysically relevant acids, formic acid (HCOOH) and thioformic acid (HC(O)SH), where the latter has recently been discovered in space. We also searched for these molecules towards the hot core G31.41+0.31 to compare their abundances with the expected theoretical isomerization results. Our results demonstrate that these isomerizations are viable in the conditions of the ISM due to ground-state tunneling effects, which allow the system to reach the thermodynamic equilibrium at moderately low temperatures. At very low temperatures (Tkin 10 K), the reaction rate constants for the cis to trans isomerizations are very small, which implies that the cis isomers should not be formed under cold ISM conditions. This is in disagreement with observations of the cis/trans isomers of HCOOH in cold cores where the cis isomer is found to be 5-6% the trans isomer. At high temperatures (150-300 K), our theoretical data not only match the observed behaviour of the trans/cis abundance ratios for HCOOH (the cis form is undetected), but they support our tentative detection of the trans and, for the first time in the insterstellar medium, of the cis isomer of HC(O)SH towards the hot molecular core G31.41+0.31 (with a measured trans/cis abundance ratio of 3.7). While the trans/cis ratio for HC(O)SH in the ISM depends on the relative stability of the isomers, the trans/cis ratio for HCOOH cannot be explained by isomerization, and it is determined by other competitive chemical processes

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arXiv2021

ALCHEMI: an ALMA Comprehensive High-resolution Extragalactic Molecular Inventory. Survey presentation and first results from the ACA array

We used the Atacama Large Millimeter/submillimeter Array (ALMA), covering a nearly contiguous 289 GHz frequency range between 84.2 and 373.2 GHz, to image the continuum and spectral line emission at 1.6\arcsec ($\sim 28$ pc) resolution down to a sensitivity of $30-50$ mK. This article describes the ALMA Comprehensive High-resolution Extragalactic Molecular Inventory (ALCHEMI) Large Program. We focus on the analysis of the spectra extracted from the $15''$ ($\sim255$ pc) resolution ALMA Compact Array data. We model the molecular emission assuming local thermodynamic equilibrium with 78 species detected. Additionally, multiple hydrogen and helium recombination lines are identified. Spectral lines contribute 5 to 36\% of the total emission in frequency bins of 50 GHz. We report the first extragalactic detections of C$_2$H$_5$OH, HOCN, HC$_3$HO, and several rare isotopologues. Isotopic ratios of carbon, oxygen, sulfur, nitrogen and silicon were measure with multiple species. Infrared pumped vibrationaly excited HCN, HNC, and HC$_3$N emission, originating in massive star formation locations, is clearly detected at low resolution, while we do not detect it for HCO$^+$. We suggest high temperature conditions in these regions driving a seemingly "carbon-rich" chemistry which may also explain the observed high abundance of organic species close to those in Galactic hot cores. The $L_{vib}/L_{IR}$ ratio is used as a proxy to estimate a $3\%$ contribution from proto super star cluster to the global infrared emission. Measured isotopic ratios with high dipole moment species agree with those within the central kiloparsec of the Galaxy, while those derived from $\rm^{13}C^{18}O$ are a factor of 5 larger, confirming the existence of multiple ISM components within NGC 253 with different degrees of nucleosynthesis enrichment. ALCHEMI provides a template for early Universe galaxies.

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arXiv2021

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

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

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arXiv2021

The GUAPOS project II. A comprehensive study of peptide-like bond molecules

Peptide-like bond molecules, which can take part to the formation of proteins in a primitive Earth environment, have been detected up to now only towards a few sources. We present a study of HNCO, HC(O)NH$_{2}$, CH$_{3}$NCO, CH$_{3}$C(O)NH$_{2}$, CH$_{3}$NHCHO, CH$_{3}$CH$_{2}$NCO, NH$_{2}$C(O)NH$_{2}$, NH$_{2}$C(O)CN, and HOCH$_{2}$C(O)NH$_{2}$ towards the hot core G31.41+0.31. We have used the spectrum obtained from the ALMA 3mm spectral survey GUAPOS, with an angular resolution of 1.2"$\times$1.2" ($\sim$4500 au), to derive column densities of all the molecular species, together with other 0.2"$\times$0.2" ($\sim$750 au) ALMA observations to study the morphology of HNCO, HC(O)NH$_{2}$ and CH$_{3}$C(O)NH$_{2}$. We have detected HNCO, HC(O)NH$_{2}$, CH$_{3}$NCO, CH$_{3}$C(O)NH$_{2}$, and CH$_{3}$NHCHO, for the first time all together outside the Galactic center. We have obtained molecular fractional abundances with respect to H$_{2}$ from 10$^{-7}$ down to a few 10$^{-9}$ and with respect to CH$_{3}$OH from 10$^{-3}$ to $\sim$4$\times$10$^{-2}$. From the comparison with other sources, we find that regions in an earlier stage of evolution, such as pre-stellar cores, show abundances at least two orders of magnitude lower than those in hot cores, hot corinos or shocked regions. Moreover, molecular abundance ratios towards different sources are found to be consistent between them within $\sim$1 order of magnitude, regardless of the physical properties (e.g. different masses and luminosities), or the source position throughout the Galaxy. New correlations between pairs of molecular abundances have also been found. These results suggest that all these species are formed on grain surfaces in early evolutionary stages of molecular clouds, and that they are subsequently released back to the gas-phase through thermal desorption or shock-triggered desorption.

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arXiv2021

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

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

astro-ph.GA↗

arXiv2021

The TOPGöt high-mass star-forming sample. I. Methyl cyanide emission as tracer of early phases of star formation

The TOPGöt project studies a sample of 86 high-mass star-forming regions in different evolutionary stages from starless cores to ultra compact HII regions. The aim of the survey is to analyze different molecular species in a statistically significant sample to study the chemical evolution in high-mass star-forming regions, and identify chemical tracers of the different phases. The sources have been observed with the IRAM 30m telescope in different spectral windows at 1, 2, and 3 mm. In this first paper, we present the sample and analyze the spectral energy distributions (SEDs) of the TOPGöt sources to derive physical parameters. We use the MADCUBA software to analyze the emission of methyl cyanide (CH$_3$CN), a well-known tracer of high-mass star formation. The emission of the $\rm{CH_3CN(5_{K}-4_{K})}$ K-transitions has been detected towards 73 sources (85% of the sample), with 12 non-detections and one source not observed in the frequency range of $\rm{CH_3CN(5_{K}-4_{K})}$. The emission of CH$_3$CN has been detected towards all evolutionary stages, with the mean abundances showing a clear increase of an order of magnitude from high-mass starless-cores to later evolutionary stages. We found a conservative abundance upper limit for high-mass starless cores of $X_{\rm CH_3CN}<4.0\times10^{-11}$, and a range in abundance of $4.0\times10^{-11}<X_{\rm CH_3CN}<7.0\times10^{-11}$ for those sources that are likely high-mass starless cores or very early high-mass protostellar objects. In fact, in this range of abundance we have identified five sources previously not classified as being in a very early evolutionary stage. The abundance of $\rm{CH_3CN}$ can thus be used to identify high-mass star-forming regions in early phases of star-formation.

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arXiv2021

The Distribution and Origin of C$_2$H in NGC 253 from ALCHEMI

Observations of chemical species can provide an insight into the physical conditions of the emitting gas but it is important to understand how their abundances and excitation vary within different heating environments. C$_2$H is a molecule typically found in PDR regions of our own Galaxy but there is evidence to suggest it also traces other regions undergoing energetic processing in extragalactic environments. As part of the ALCHEMI ALMA large program, the emission of C$_2$H in the central molecular zone of the nearby starburst galaxy NGC 253 was mapped at 1.6 " (28 pc) resolution and characterized to understand its chemical origins. Spectral modelling of the N=1-0 through N=4-3 rotational transitions of C$_2$H was used to derive the C$_2$H column densities towards the dense clouds in NGC 253. Chemical modelling, including PDR, dense cloud, and shock models were then used to investigate the chemical processes and physical conditions that are producing the molecular emission. We find high C$_2$H column densities of $\sim 10^{15} cm^{-3}$ detected towards the dense regions of NGC 253. We further find that these column densities cannot be reproduced by assuming that the emission arises from the PDR regions at the edge of the clouds. Instead, we find that the C$_2$H abundance remains high even in the high visual extinction interior of these clouds and that this is most likely caused by a high cosmic-ray ionization rate.

astro-ph.GA↗

arXiv2021

First survey of HCNH$^+$ in high-mass star-forming cloud cores

Most stars in the Galaxy, including the Sun, were born in high-mass star-forming regions. It is hence important to study the chemical processes in these regions to better understand the chemical heritage of both the Solar System and most stellar systems in the Galaxy. The molecular ion HCNH+ is thought to be a crucial species in ion-neutral astrochemical reactions, but so far it has been detected only in a handful of star-forming regions, and hence its chemistry is poorly known. We have observed with the IRAM-30m Telescope 26 high-mass star-forming cores in different evolutionary stages in the J=3-2 rotational transition of HCNH+. We report the detection of HCNH+ in 16 out of 26 targets. This represents the largest sample of sources detected in this molecular ion so far. The fractional abundances of HCNH+, [HCNH+], w.r.t. H2, are in the range 0.9 - 14 X $10^{-11}$, and the highest values are found towards cold starless cores. The abundance ratios [HCNH+]/[HCN] and [HCNH+]/[HCO+] are both < 0.01 for all objects except for four starless cores, for which they are well above this threshold. These sources have the lowest gas temperature in the sample. We run two chemical models, a "cold" one and a "warm" one, which attempt to match as much as possible the average physical properties of the cold(er) starless cores and of the warm(er) targets. The reactions occurring in the latter case are investigated in this work for the first time. Our predictions indicate that in the warm model HCNH+ is mainly produced by reactions with HCN and HCO+, while in the cold one the main progenitor species of HCNH+ are HCN+ and HNC+. The results indicate that the chemistry of HCNH+ is different in cold/early and warm/evolved cores, and the abundance ratios [HCNH+]/[HCN] and [HCNH+]/[HCO+] is a useful astrochemical tool to discriminate between different evolutionary phases in the process of star formation.

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arXiv2020

Carbon isotopic fractionation in molecular clouds

C-fractionation has been studied from a theoretical point of view with different models of time-dependent chemistry, including both isotope-selective photodissociation and low-temperature isotopic exchange reactions. Recent chemical models predict that the latter may lead to a depletion of $^{13}$C in nitrile-bearing species, with $^{12}$C/$^{13}$C ratios two times higher than the elemental abundance ratio of 68 in the local ISM. Since the carbon isotopic ratio is commonly used to evaluate the $^{14}$N/$^{15}$N ratios with the double-isotope method, it is important to study C-fractionation in detail to avoid incorrect assumptions. In this work we implemented a gas-grain chemical model with new isotopic exchange reactions and investigated their introduction in the context of dense and cold molecular gas. In particular, we investigated the $^{12}$C/$^{13}$C ratios of HNC, HCN, and CN using a grid of models, with temperatures and densities ranging from 10 to 50 K and 2$\times$10$^{3}$ to 2$\times$10$^{7}$ cm$^{-3}$, respectively. We suggest a possible $^{13}$C exchange through the $^{13}$C + C$_{3}$ $\rightarrow$ $^{12}$C +$^{13}$CC$_{2}$ reaction, which does not result in dilution, but rather in $^{13}$C enhancement, for molecules formed starting from atomic carbon. This effect is efficient in a range of time between the formation of CO and its freeze-out on grains. Furthermore, we show that the $^{12}$C/$^{13}$C ratios of nitriles are predicted to be a factor 0.8-1.9 different from the local value of 68 for massive star-forming regions. This result also affects the $^{14}$N/$^{15}$N ratio: a value of 330 obtained with the double-isotope method is predicted to be 260-1150, depending on the physical conditions. Finally, we studied the $^{12}$C/$^{13}$C ratios by varying the cosmic-ray ionization rate: the ratios increase with it because of secondary photons and cosmic-ray reactions.

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arXiv2020

The GUAPOS project: G31.41+0.31 Unbiased ALMA sPectral Observational Survey -- I. Isomers of C$_{2}$H$_{4}$O$_{2}$

Understanding the degree of chemical complexity that can be reached in star-forming regions, together with the identification of precursors of the building blocks of life in the interstellar medium, is one of the goals of astrochemistry. Unbiased spectral surveys with large bandwidth and high spectral resolution are thus needed, to resolve line blending in chemically rich sources and identify complex organic molecules. This kind of observations has been successfully carried out, mainly towards the Galactic Center, a region that shows peculiar environmental conditions. We present an unbiased spectral survey at 3mm of one of the most chemically rich hot molecular cores located outside the Galactic Center, in the high-mass star-forming region G31.41+0.31. In this first paper, we present the survey and discuss the detection of the 3 isomers of C$_{2}$H$_{4}$O$_{2}$: methyl formate, glycolaldehyde and acetic acid. Observations were carried out with ALMA and cover the entire Band 3 from 84 to 116 GHz with an angular resolution of $1.2^{''}$x$1.2^{''}$ and a spectral resolution of $\sim0.488$ MHz. The transitions of the 3 molecules have been analyzed with the software XCLASS. All three isomers were detected and methyl formate and acetic acid abundances in G31 are the highest detected up to now, if compared to sources in literature. The size of the emission varies among the three isomers with acetic acid showing the most compact emission while methyl formate the most extended. The comparison with chemical models suggests the necessity of grain-surface routes for the formation of methyl formate in G31, while for glycolaldehyde both scenarios could be feasible. Proposed grain-surface reaction for acetic acid is not able to reproduce the observed abundance in this work, while gas-phase scenario should be further tested due to large uncertainties.

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arXiv2020

Extensive ro-vibrational analysis of deuterated-cyanoacetylene (DC$_3$N) from millimeter-wavelengths to the infrared domain

Cyanoacetylene, the simplest cyanopolyyne, is an abundant interstellar molecule commonly observed in a vast variety of astronomical sources. Despite its importance as a potential tracer of the evolution of star-forming processes, the deuterated form of cyanoacetylene is less observed and less studied in the laboratory than the main isotopologue. Here, we report the most extensive spectroscopic characterization of DC$_3$N to date, from the millimeter domain to the infrared region. Rotational and ro-vibrational spectra have been recorded using millimeter-wave frequency-modulation and Fourier-transform infrared spectrometers, respectively. All the vibrational states with energy up to 1015 cm$^{-1}$ have been analyzed in a combined fit, where the effects due to anharmonic resonances have been adequately accounted for. The analysis contains over 6500 distinct transition frequencies, from which all the vibrational energies have been determined with good precision for many fundamental, overtone, and combination states. This work provides a comprehensive line catalog for astronomical observations of DC$_3$N

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arXiv2020

Evolutionary study of complex organic molecules in high-mass star-forming regions

We have studied four complex organic molecules (COMs), methyl formate ($CH_3OCHO$), dimethyl ether ($CH_3OCH_3$), formamide ($NH_2CHO$), and ethyl cyanide ($C_2H_5CN$), towards a large sample of 39 high-mass star-forming regions representing different evolutionary stages, from early to evolved phases. We aim to identify potential correlations between the molecules and to trace their evolutionary sequence through the star formation process. We analysed spectra obtained at 3, 2, and 0.9 mm with the IRAM-30m telescope. We derived the main physical parameters for each species by fitting the molecular lines. We compared them and evaluated their evolution, also taking several other interstellar environments into account. We report detections in 20 sources, revealing a clear dust absorption effect on column densities. Derived abundances are ~$10^{-10}-10^{-7}$ for $CH_3OCHO$ and $CH_3OCH_3$, ~$10^{-12}-10^{-10}$ for $NH_2CHO$, and ~$10^{-11}-10^{-9}$ for $C_2H_5CN$. The abundances of $CH_3OCHO$, $CH_3OCH_3$, and $C_2H_5CN$ are very strongly correlated (r>0.92) across ~4 orders of magnitude. $CH_3OCHO$ and $CH_3OCH_3$ show the strongest correlations in most parameters, and a nearly constant ratio (~1) over a remarkable ~9 orders of magnitude in luminosity for a wide variety of sources: pre-stellar to evolved cores, low- to high-mass objects, shocks, Galactic clouds, and comets. This indicates that COMs chemistry is likely early developed and then preserved through evolved phases. Moreover, the molecular abundances clearly increase with evolution. We consider $CH_3OCHO$ and $CH_3OCH_3$ to be most likely chemically linked: they could e.g. share a common precursor, or be formed one from the other. We propose a general scenario for all COMs, involving a formation in the cold, earliest phases of star formation and a following increasing desorption with the progressive heating of the evolving core.

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arXiv2020

DC$_3$N observations towards high-mass star-forming regions

We present the study of deuteration of cyanoacetylene (HC$_3$N) towards a sample of 28 high-mass star-forming cores divided into different evolutionary stages, from starless to evolved protostellar cores. We report for the first time the detection of DC$_3$N towards 15 high-mass cores. The abundance ratios of DC$_3$N with respect HC$_3$N range in the interval 0.003$-$0.022, lower than those found in low-mas protostars and dark clouds. No significant trend with the evolutionary stage, or with the kinetic temperature of the region, has been found. We compare the level of deuteration of HC$_3$N with those of other molecules towards the same sample, finding weak correlation with species formed only or predominantly in gas phase (N$_2$H$^+$ and HNC, respectively), and no correlation with species formed only or predominantly on dust grains (CH$_3$OH and NH$_3$, respectively). We also present a single-dish map of DC$_3$N towards the protocluster IRAS 05358+3543, which shows that DC$_3$N traces an extended envelope ($\sim$0.37 pc) and peaks towards two cold condensations separated from the positions of the protostars and the dust continuum. The observations presented in this work suggest that deuteration of HC$_3$N is produced in the gas of the cold outer parts of massive star-forming clumps, giving us an estimate of the deuteration factor prior to the formation of denser gas.

astro-ph.GA↗

arXiv2020

No nitrogen fractionation on 600 au scale in the Sun progenitor analogue OMC-2 FIR4

We show the first interferometric maps of the 14N/15N ratio obtained with the Atacama Large Millimeter Array (ALMA) towards the Solar-like forming protocluster OMC-2 FIR4. We observed N2H+, 15NNH+, N15NH+ (1-0), and N2D+ (2-1), from which we derive the isotopic ratios 14N/15N and D/H. The target is one of the closest analogues of the environment in which our Sun may have formed. The ALMA images, having synthesised beam corresponding to ~600 au, show that the emission of the less abundant isotopologues is distributed in several cores of ~10" (i.e. ~0.02~pc or 4000 au) embedded in a more extended N2H+ emission. Overall, our results indicate that: (1) 14N/15N does not change across the region at core scales, and (2) 14N/15N does not depend on temperature variations. Our findings also suggest that the 14N/15N variations found in pristine Solar System objects are likely not inherited from the protocluster stage, and hence their reason has to be found elsewhere.

astro-ph.SR↗

arXiv2019

First interferometric study of enhanced N-fractionation in N$_{2}$H$^{+}$: the high-mass star-forming region IRAS 05358+3543

Nitrogen (N) fractionation is used as a tool to search for a link between the chemical history of the Solar System and star-forming regions. A large variation of $^{14}$N/$^{15}$N is observed towards different astrophysical sources, and current chemical models cannot reproduce it. With the advent of high angular resolution radiotelescopes it is now possible to search for N-fractionation at core scales. We present IRAM NOEMA observations of the J=1-0 transition of N$_{2}$H$^{+}$, $^{15}$NNH$^{+}$ and N$^{15}$NNH$^{+}$ towards the high-mass protocluster IRAS 05358+3543. We find $^{14}$N/$^{15}$N ratios that span from $\sim$100 up to $\sim$220 and these values are lower or equal than those observed with single-dish observations towards the same source. Since N-fractionation changes across the studied region, this means that it is regulated by local environmental effects. We find also the possibility, for one of the four cores defined in the protocluster, to have a more abundant $^{15}$NNH$^{+}$ with respect to N$^{15}$NNH$^{+}$. This is another indication that current chemical models may be missing chemical reactions or may not take into account other mechanisms, like photodissociation or grain surface chemistry, that could be important.

astro-ph.SR↗