Dark Molecular Clouds Research Articles

The Transition from Diffuse Molecular Gas to Molecular Cloud Material in Taurus

Abstract We study four lines of sight that probe the transition from diffuse molecular gas to molecular cloud material in Taurus. Measurements of atomic and molecular absorption are used to infer the distribution of species and the physical conditions toward stars behind the Taurus Molecular Cloud (TMC). New high-resolution spectra at visible and near-IR wavelengths of interstellar Ca ii, Ca i, K i, CH, CH+, C2, CN, and CO toward HD 28975 and HD 29647 are combined with data at visible wavelengths and published CO results from ultraviolet measurements for HD 27778 and HD 30122. Gas densities and temperatures are inferred from C2, CN, and CO excitation and CN chemistry. Our results for HD 29647 are noteworthy because the CO column density is 1018 cm−2 while C2 and CO excitation reveals a temperature of 10 K and a density of ∼1000 cm−3, more like conditions found in dark molecular clouds. Similar results arise from our chemical analysis for CN through reactions involving observations of CH, C2, and NH. Enhanced potassium depletion and a reduced CH/H2 column density ratio also suggest the presence of a dark cloud. The directions toward HD 27778 and HD 30122 probe molecule-rich diffuse clouds, which can be considered CO-dark gas, while the sight line toward HD 28975 represents an intermediate case. Maps of dust temperature help refine the description of the material along the four sight lines and provide an estimate of the distance between HD 29647 and a clump in the TMC. An appendix provides results for the direction toward HD 26571; this star also probes diffuse molecular gas.

Aromatics and Cyclic Molecules in Molecular Clouds: A New Dimension of Interstellar Organic Chemistry.

Astrochemistry lies at the nexus of astronomy, chemistry, and molecular physics. On the basis of precise laboratory data, a rich collection of more than 200 familiar and exotic molecules have been identified in the interstellar medium, the vast majority by their unique rotational fingerprint. Despite this large body of work, there is scant evidence in the radio band for the basic building blocks of chemistry on earth-five- and six-membered rings-despite long-standing and sustained efforts during the past 50 years. In contrast, a peculiar structural motif, highly unsaturated carbon in a chainlike arrangement, is instead quite common in space. The recent astronomical detection of cyanobenzene, the simplest aromatic nitrile, in the dark molecular cloud TMC-1, and soon afterward in additional prestellar and possibly protostellar sources, establishes that aromatic chemistry is likely widespread in the earliest stages of star formation. The subsequent discovery of cyanocyclopentadienes and even cyanonaphthalenes in TMC-1 provides further evidence that organic molecules of considerable complexity are readily synthesized in regions with high visual extinction but where the low temperature and pressure are remarkably low. This review focuses on laboratory efforts now underway to understand the rich transition region between linear and planar carbon structures using microwave spectroscopy. We present key features, advantages, and disadvantages of current detection methods, a discussion of the types of molecules found in space and in the laboratory, and approaches under development to identify entirely new species in complex mixtures. Studies focusing on the cyanation of hydrocarbons and the formation of benzene from acyclic precursors are highlighted, as is the role that isotopic studies might play in elucidating the chemical pathways to ring formation.

Gas phase Elemental abundances in Molecular cloudS (GEMS)

Context. Carbon monosulphide (CS) is among the most abundant gas-phase S-bearing molecules in cold dark molecular clouds. It is easily observable with several transitions in the millimeter wavelength range, and has been widely used as a tracer of the gas density in the interstellar medium in our Galaxy and external galaxies. However, chemical models fail to account for the observed CS abundances when assuming the cosmic value for the elemental abundance of sulfur. Aims. The CS+O → CO + S reaction has been proposed as a relevant CS destruction mechanism at low temperatures, and could explain the discrepancy between models and observations. Its reaction rate has been experimentally measured at temperatures of 150−400 K, but the extrapolation to lower temperatures is doubtful. Our goal is to calculate the CS+O reaction rate at temperatures <150 K which are prevailing in the interstellar medium. Methods. We performed ab initio calculations to obtain the three lowest potential energy surfaces (PES) of the CS+O system. These PESs are used to study the reaction dynamics, using several methods (classical, quantum, and semiclassical) to eventually calculate the CS + O thermal reaction rates. In order to check the accuracy of our calculations, we compare the results of our theoretical calculations for T ~ 150−400 K with those obtained in the laboratory. Results. Our detailed theoretical study on the CS+O reaction, which is in agreement with the experimental data obtained at 150–400 K, demonstrates the reliability of our approach. After a careful analysis at lower temperatures, we find that the rate constant at 10 K is negligible, below 10−15 cm3 s−1, which is consistent with the extrapolation of experimental data using the Arrhenius expression. Conclusions. We use the updated chemical network to model the sulfur chemistry in Taurus Molecular Cloud 1 (TMC 1) based on molecular abundances determined from Gas phase Elemental abundances in Molecular CloudS (GEMS) project observations. In our model, we take into account the expected decrease of the cosmic ray ionization rate, ζH2, along the cloud. The abundance of CS is still overestimated when assuming the cosmic value for the sulfur abundance.

Quantification of the Role of Chemical Desorption in Molecular Clouds.

ConspectusDark molecular clouds have low temperatures of approximately 10 K and experience very little UV irradiation. These clouds are the birthplace of new stars and consist of gas and dust particles. The latter can act as a meeting place to facilitate surface chemistry to form saturated molecules such as formaldehyde, methyl formate, and dimethyl ether. These complex organic molecules or COMs become encapsulated in the ice that forms on the dust grains, and these ices are the precursor for cometary ices and other icy bodies. They likely played a role in bringing material to the early earth.Although these COMs are likely formed on the surfaces of dust grains, several of them have been detected in the gas phase. This means that they have desorbed from the grain under these cold, dark conditions where thermal desorption and photodesorption are negligible. It has been speculated that reactive, or chemical, desorption is responsible for the high gas-phase abundance. After a surface reaction, its products might be vibrationally, translationally, and/or rotationally excited. Dissipation of the excess energy to translational energy can briefly increase the desorption rate, leading to chemical desorption. Astrochemical modellers have added terms to their rate equations to account for this effect. These terms, however, have had little experimental or theoretical verification.In this Account, we use classical molecular dynamics (MD) simulations to give adsorbed molecules a fixed amount of energy as a proxy for excess energy and to record whether this leads to desorption. The excitation energy can be varied freely while keeping all other variables constant. This allows for the study of trends rather than being limited to a single reaction and a single system. The focus is on the dependence of the chemical desorption on the excitation energy, excitation type, and binding energy. Rotational and vibrational excitation was explicitly taken into account. An analytical expression for the chemical desorption probability was obtained in this way. It depends on the binding energy and reaction enthalpy. This expression was then implemented in a gas–grain astrochemical code to simulate the chemical evolution of a dark molecular cloud, and the results were compared against observational abundances of COMs in three different molecular clouds. The results with our new expression based on the MD simulations show good agreement for all species except H2CO, which has both gas-phase and surface-formation routes. This is a significant improvement over models without chemical desorption or with other expressions for chemical desorption, as frequently used by other authors. It is encouraging to see that a general description with a firmer theoretical basis leads to a significant improvement. Understanding chemical desorption can help to explain the unexpectedly high gas-phase abundance of some COMs, and chemical desorption also provides a link between the gas phase and the ice mantle, and its understanding might help in creating a diagnostic tool to learn more about the ice composition.

Cation, Anion, and Radical Isomers of C4H4N: Computational Characterization and Implications for Astrophysical and Planetary Environments.

Nitrogen-containing ions and molecules in the gas phase have been detected in non-Earth environments such as dark molecular clouds and more recently in the atmosphere of Saturn's moon Titan. These molecules may serve as precursors to larger heterocyclic structures that provide the foundation of complex biological molecules. On Titan, molecules of m/z 66 have been detected by the Cassini mission, and species of the empirical formula C4H4N may contribute to this signature. We have characterized seven isomers of C4H4N in anionic, neutral radical, and cationic states using density functional theory. Structures were optimized using the range-separated hybrid ωB97X-V with the cc-pVTZ and aug-cc-pVTZ basis sets. Anionic and radical C4H4N favor cyclic structures with aromatic and quasi-aromatic electron arrangements, respectively. Interestingly, ionization from the radical surface to the cation induces significant changes in structural stability, and the global minimum for positively charged isomers is CH2CCHCNH+, a pseudo-linear species reminiscent of cyanoallene. Select formation pathways to these structures from Titan's existing or postulated gas-phase species, reactions that are also relevant for other astrophysical environments, are discussed. By characterizing C4H4N isomers, we have identified energetically stable anionic, radical, and cationic structures that may be present in Titan's atmosphere and dark molecular clouds.

Formation of COMs through CO hydrogenation on interstellar grains

Context. Glycoaldehyde, ethylene glycol, and methyl formate are complex organic molecules that have been observed in dark molecular clouds. Because there is no efficient gas-phase route to produce these species, it is expected that a low-temperature surface route existst that does not require energetic processing. CO hydrogenation experiments at low temperatures showed that this is indeed the case. Glyoxal can form through recombination of two HCO radicals and is then further hydrogenated. Aims. Here we aim to constrain the methyl formate, glycolaldehyde, and ethylene glycol formation on the surface of interstellar dust grains through this cold and dark formation route. We also probe the dependence of the grain mantle composition on the initial gas-phase composition and the dust temperature. Methods. A full CO hydrogenation reaction network was built based on quantum chemical calculations for the rate constants and branching ratios. This network was used in combination with a microscopic kinetic Monte Carlo simulation to simulate ice chemistry, taking into account all positional information. After benchmarking the model against CO-hydrogenation experiments, simulations under molecular cloud conditions were performed. Results. Glycoaldehyde, ethylene glycol, and methyl formate are formed in all interstellar conditions we studied, even at temperatures as low as 8 K. This is because the HCO + HCO reaction can occur when HCO radicals are formed close to each other and do not require to diffuse. Relatively low abundances of methyl formate are formed. The final COM abundances depend more on the H-to-CO ratio and less on temperature. Only above 16 K, where CO build-up is less efficient, does temperature start to play a role. Molecular hydrogen is predominantly formed through abstraction reactions on the surface. The most important reaction leading to methanol is H2CO + CH3O → HCO + CH3OH. Our simulations are in agreement with observed COM ratios for mantles that have been formed at low temperatures.

Gas-phase kinetics of CH3CHO with OH radicals between 11.7 and 177.5 K.

Gas-phase reactions in the interstellar medium (ISM) are a source of molecules in this environment. The knowledge of the rate coefficient for neutral-neutral reactions as a function of temperature, k(T), is essential to improve astrochemical models. In this work, we have experimentally measured k(T) for the reaction between the OH radical and acetaldehyde, both present in many sources of the ISM. Laser techniques coupled to a CRESU system were used to perform the kinetic measurements. The obtained modified Arrhenius equation is k(T = 11.7-177.5 K) = (1.2 ± 0.2) × 10-11 (T/300 K)-(1.8±0.1) exp-{(28.7 ± 2.5)/T} cm3 molecule-1 s-1. The k(T) value of the title reaction has been measured for the first time below 60 K. No pressure dependence of k(T) was observed at ca. 21, 50, 64 and 106 K. Finally, a pure gas-phase model indicates that the title reaction could become the main CH3CO formation pathway in dark molecular clouds, assuming that CH3CO is the main reaction product at 10 K.

Low-temperature chemistry induced by cosmic rays: positive and negative ion desorption from nitrile-bearing astrophysical ice analogues

ABSTRACT In cold core of dark molecular clouds, where the UV radiation from external sources is strongly attenuated, cosmic rays can induce chemical reactions on the surface of ice-covered grains promoting the ejection of the processed material to the gas phase. We report the positive and negative secondary ion emission from pure CH3CN, C2H3CN, and i-C3H7CN ices due to the bombardment of heavy ions (252Cf fission fragments), simulating the incidence of cosmic rays on to icy surfaces. The secondary ions emitted from each sample were analysed by time-of-flight mass spectrometry, using Plasma Desorption Mass Spectrometry technique. Several ionic species were identified, indicating strong fragmentation on the frozen surface. Proton-transfer processes are suggested to play a role for positive ion desorption, as evidenced by the protonated RCNH+ parent molecules and (RCN)nH+ ionic clusters. The high electron affinity of the cyano radical seems to contribute to the strong emission of CN−, as well as anions attributed to the CHmCN− fragment and (RCN)nCN− cluster series. Sputtering and desorption of ion clusters (positive and negative) induced by heavy ion bombardment are suggested to constitute a route by which new neutral or ionized molecular species may be delivered to the gas phase where thermal desorption is negligible.

Formation of Massive Protostellar Clusters—Observations of Massive 70 μm Dark Molecular Clouds

Abstract We present Submillimeter Array observations of seven massive molecular clumps that are dark in the far-infrared for wavelengths up to 70 μm. Our 1.3 mm continuum images reveal 44 dense cores, with gas masses ranging from 1.4 to 77.1 M ⊙. Twenty-nine dense cores have masses greater than 8 M ⊙ and the other 15 dense cores have masses between 1.4 and 7.5 M ⊙. Assuming the core density follows a power law in radius ρ ∝ r −b , the index b is found to be between 0.6 and 2.1, with a mean value of 1.3. The virial analysis reveals that the dense cores are not in virial equilibrium. CO outflow emission was detected toward six out of seven molecular clumps and associated with 17 dense cores. For five of these cores, CO emissions appear to have line wings at velocities of greater than 30 km s−1 with respect to the source systemic velocity, which indicates that most of the clumps harbor protostars and thus are not quiescent in star formation. The estimated outflow timescale increases with core mass, which likely indicates that massive cores have longer accretion timescales than less massive ones. The fragmentation analysis shows that the masses of low-mass and massive cores are roughly consistent with thermal and turbulent Jeans masses, respectively.

The ortho-to-para ratio of water in interstellar clouds

The nuclear-spin chemistry of interstellar water is investigated using the University of Grenoble Alpes Astrochemical Network (UGAN). This network includes reactions involving the different nuclear-spin states of the hydrides of carbon, nitrogen, oxygen and sulphur, as well as their deuterated forms. Nuclear-spin selection rules are implemented within the scrambling hypothesis for reactions involving up to seven protons. The abundances and ortho-to-para ratios (OPRs) of gas-phase water and water ions (H$_2$O$^+$ and H$_3$O$^+$) are computed under the steady-state conditions representative of a dark molecular cloud and during the early phase of gravitational collapse of a prestellar core. The model incorporates the freezing of the molecules on to grains, simple grain surface chemistry and cosmic-ray induced and direct desorption of ices. The predicted OPRs are found to deviate significantly from both thermal and statistical values and to be independent of temperature below $\sim $30~K. The OPR of H$_2$O is shown to lie between 1.5 and 2.6, depending on the spin-state of H$_2$, in good agreement with values derived in translucent clouds with relatively high extinction. In the prestellar core collapse calculations, the OPR of H$_2$O is shown to reach the statistical value of 3 in regions with severe depletion ($n_{\rm H}> 10^7$~cm$^{-3}$). We conclude that a low water OPR ($\lesssim 2.5$) is consistent with gas-phase ion-neutral chemistry and reflects a gas with OPR(H$_2)\lesssim 1$. Available OPR measurements in protoplanetary disks and comets are finally discussed.

Catching the Birth of a Dark Molecular Cloud for the First Time

Abstract The majority of hydrogen in the interstellar medium (ISM) is in atomic form. The transition from atoms to molecules and, in particular, the formation of the H2 molecule, is a key step in cosmic structure formation en route to stars. Quantifying H2 formation in space is difficult, due to the confusion in the emission of atomic hydrogen (H i) and the lack of a H2 signal from the cold ISM. Here we present the discovery of a rare, isolated dark cloud currently undergoing H2 formation, as evidenced by a prominent “ring” of H i self-absorption. Through a combined analysis of H i narrow self-absorption, CO emission, dust emission, and extinction, we directly measured, for the first time, the [H i]/[H2] abundance varying from 2% to 0.2%, within one region. These measured H i abundances are orders of magnitude higher than usually assumed initial conditions for protoplanetary disk models. None of the fast cloud formation model could produce such low atomic hydrogen abundance. We derived a cloud formation timescale of ∼6 × 106 years, consistent with the global Galactic star formation rate, and favoring the classical star formation picture over fast star formation models. Our measurements also help constrain the H2 formation rate, under various ISM conditions.

Associative detachment (AD) paths for H and CN- in the gas-phase: astrophysical implications.

The direct dynamical paths leading to Associative Detachment (AD) in the gas-phase, and specifically in the low-temperature regions of the Dark Molecular Clouds (DMC) in the ISM, or in cold trap laboratory experiments, are investigated with quantum chemical methods by using a high-level multi-reference Configuration Interaction (CI) approach that employs single and double excitations plus Davidson perturbative correction [MRSDCI(Q)] and the d-aug-cc-pV5Z basis set. The potential energy curves for H + CN- are constructed for different directions of the H partner approaching the CN- anion within the framework of the Born-Oppenheimer approximation. The present calculations found that the AD energetics at low temperature becomes favorable only along a selected range of approaching directions, thus showing that there is a preferred path of forming HCN at low temperatures, while that of forming its HNC isomer is found to be energetically forbidden. Given the existence in the ISM of different HCN/HNC ratios in different environments, we discuss the implications of our findings for selective formation of either isomer in the low-temperature conditions of the molecular cloud cores.

A new method to unveil embedded stellar clusters

In this paper we present a novel method to identify and characterize stellar clusters deeply embedded in a dark molecular cloud. The method is based on measuring stellar surface density in wide-field infrared images using star counting techniques. It takes advantage of the differing H-band luminosity functions (HLFs) of field stars and young stellar populations and is able to statistically associate each star in an image as a member of either the background stellar population or a young stellar population projected on or near the cloud. Moreover, the technique corrects for the effects of differential extinction toward each individual star. We have tested this method against simulations as well as observations. In particular, we have applied the method to 2MASS point sources observed in the Orion A and B complexes, and the results obtained compare very well with those obtained from deep Spitzer and Chandra observations where presence of infrared excess or X-ray emission directly determines membership status for every star. Additionally, our method also identifies unobscured clusters and a low resolution version of the Orion stellar surface density map shows clearly the relatively unobscured and diffuse OB 1a and 1b sub-groups and provides useful insights on their spatial distribution.

Formation of Anionic C, N-bearing Chains in the Interstellar Medium via Reactions of H− with HCxN for Odd-valued x from 1 to 7

Abstract We investigate the relative efficiencies of low-temperature chemical reactions in the interstellar medium with H− anion reacting in the gas phase with cyanopolyyne neutral molecules, leading to the formation of anionic linear chains of different lengths and of H2. All the reactions turn out to be without barriers, highly exothermic reactions that provide a chemical route to the formation of anionic chains of the same length. Some of the anions have been observed in the dark molecular clouds and in the diffuse interstellar envelopes. Quantum calculations are carried out for the corresponding reactive potential energy surfaces for all the odd-numbered members of the series (x = 1, 3, 5, 7). We employ the minimum energy paths to obtain the relevant transition state configurations and use the latter within the variational transition state model to obtain the chemical rates. The present results indicate that at typical temperatures around 100 K, a set of significantly larger rate values exists for x = 3 and x = 5, while the rate values are smaller for CN− and . At those temperatures, however, all the rates turn out to be larger than the estimates in the current literature for the radiative electron attachment (REA) rates, thus indicating the greater importance of the present chemical path with respect to REA processes at those temperatures. The physical reasons for our findings are discussed in detail and linked with the existing observational findings.

Sensitivity Analysis of Grain Surface Chemistry to Binding Energies of Ice Species

Advanced telescopes, such as ALMA and JWST, are likely to show that the chemical universe may be even more complex than currently observed, requiring astrochemical modelers to improve their models to account for the impact of new data. However, essential input information for gas-grain models, such as binding energies of molecules to the surface, have been derived experimentally only for a handful of species, leaving hundreds of species with highly uncertain estimates. We present in this paper a systematic study of the effect of uncertainties in the binding energies on an astrochemical two-phase model of a dark molecular cloud, using the rate equations approach. A list of recommended binding energy values based on a literature search of published data is presented. Thousands of simulations of dark cloud models were run, and in each simulation a value for the binding energy of hundreds of species was randomly chosen from a normal distribution. Our results show that the binding energy of H$_{2}$ is critical for the surface chemistry. For high binding energy, H$_{2}$ freezes out on the grain forming an H$_{2}$ ice. This is not physically realistic and we suggest a change in the rate equations. The abundance ranges found are in reasonable agreement with astronomical ice observations. Pearson correlation coefficients revealed that the binding energy of HCO, HNO, CH$_{2}$, and C correlate most strongly with the abundance of dominant ice species. Finally, the formation route of complex organic molecules was found to be sensitive to the branching ratios of H$_{2}$CO hydrogenation.

Symmetry breaking and spectral considerations of the surprisingly floppy c-C3H radical and the related dipole-bound excited state of c-C3H.

The C3H radical is believed to be prevalent throughout the interstellar medium and may be involved in the formation of polycyclic aromatic hydrocarbons. C3H exists as both a linear and a cyclic isomer. The C2v cyclopropenylidenyl radical isomer was detected in the dark molecular cloud TMC-1, and the linear propenylidenyl radical isomer has been observed in various dark molecular clouds. Even though the c-C3H radical has been classified rotationally, the vibrational frequencies of this seemingly important interstellar molecule have never been directly observed. Established, highly accurate quartic force field methodologies are employed here to compute useful geometrical data, spectroscopic constants, and vibrational frequencies. The computed rotational constants are consistent with the experimental results. Consequently, the three a1 (ν1, ν2, and ν3) and one b1 (ν6) anharmonic vibrational frequencies at 3117.7 cm-1, 1564.3 cm-1, 1198.5 cm-1, and 826.7 cm-1, respectively, are reliable predictions for these, as of yet unseen, observables. Unfortunately, the two b2 fundamentals (ν4 and ν5) cannot be treated adequately in the current approach due to a flat and possible double-well potential described in detail herein. The dipole-bound excited state of the anion suffers from the same issues and may not even be bound. However, the trusted fundamental vibrational frequencies described for the neutral radical should not be affected by this deformity and are the first robustly produced for c-C3H. The insights gained here will also be applicable to other structures containing three-membered bare and exposed carbon rings that are surprisingly floppy in nature.

Hydrogenation and Deuteration of C2H2 and C2H4 on Cold Grains: A Clue to the Formation Mechanism of C2H6 with Astronomical Interest

Abstract We quantitatively investigated the hydrogen addition reactions of acetylene (C2H2) and ethylene (C2H4) on amorphous solid water (ASW) at 10 and 20 K relevant to the formation of ethane (C2H6) on interstellar icy grains. We found that the ASW surface enhances the reaction rates for C2H2 and C2H4 by approximately a factor of 2 compared to those on the pure-solid C2H2 and C2H4 at 10 K, probably due to an increase in the sticking coefficient and adsorption energy of the H atoms on ASW. In contrast to the previous proposal that the hydrogenation rate of C2H4 is orders of magnitude larger than that of C2H2, the present results show that the difference in hydrogenation rates of C2H2 and C2H4 is only within a factor of 3 on both the surfaces of pure solids and ASW. In addition, we found the small kinetic isotope effect for hydrogenation/deuteration of C2H2 and C2H4 at 10 K, despite the requirement of quantum tunneling. At 20 K, the reaction rate of deuteration becomes even larger than that of hydrogenation. These unusual isotope effects might originate from a slightly larger number density of D atoms than H atoms on ASW at 20 K. The hydrogenation of C2H2 is four times faster than CO hydrogenation and can produce C2H6 efficiently through C2H4 even in the environment of a dark molecular cloud.

EXPLORING A CHEMICAL ROUTE FOR THE FORMATION OF STABLE ANIONS OF POLYYNES [CnH− (n = 2, 4)] IN MOLECULAR CLOUDS

ABSTRACT Using quantum chemical methods, we investigate the possible outcomes of reactions with acetylene and diacetylene molecules. We find both reactions to be exothermic reactions without barriers, yielding stable anions of the corresponding polyynes: and . We show in this work that the computed chemical rates in the case of the formation of the anion would be larger than those existing for the direct radiative electron attachment (REA) process, the main mechanism generally suggested for their formation. In the case of the anion, however, the present chemical rates of formation at low T are even lower than those known for its REA process, both mechanisms being inefficient for its formation under astrochemical conditions. The present results are discussed in view of their consequences on the issue of the possible presence of such anions in the ISM environments. They clearly indicate the present chemical route to formation to be inefficient at the expected temperatures of a dark molecular cloud, whereas this is found not to be the case for the , in line with the available experimental findings.

Simultaneous hydrogenation and UV-photolysis experiments of NO in CO-rich interstellar ice analogues; linking HNCO, OCN−, NH2CHO, and NH2OH

The laboratory work presented here, simulates the chemistry on icy dust grains as typical for the 'CO freeze-out stage' in dark molecular clouds. It differs from previous studies in that solid-state hydrogenation and vacuum UV-photoprocessing are applied simultaneously to co-depositing molecules. In parallel, the reactions at play are described for fully characterized laboratory conditions. The focus is on the formation of molecules containing both carbon and nitrogen atoms, starting with NO in CO-, H2CO-, and CH3OH-rich ices at 13 K. The experiments yield three important conclusions. 1. Without UV-processing hydroxylamine (NH2OH) is formed, as reported previously. 2. With UV-processing (energetic) NH2 is formed through photodissociation of NH2OH. This radical is key in the formation of species with an N-C bond. 3. The formation of three N-C bearing species, HNCO, OCN- and NH2CHO is observed. The experiments put a clear chemical link between these species; OCN- is found to be a direct derivative of HNCO and the latter is shown to have the same precursor as formamide (NH2CHO). Moreover, the addition of VUV competing channels decreases the amount of NO molecules converted into NH2OH by at least one order of magnitude. Consequently, this decrease in NH2OH formation yield directly influences the amount of NO molecules that can be converted into HNCO, OCN- and NH2CHO.

Exploring a dynamical path for C2H− and NCO− formation in dark molecular clouds

This paper deals with the possible formation of two molecular anions often considered likely components in the physical environments of the Interstellar Medium ( ISM) : $\mathrm{C_2H^-}$ and $\mathrm{NCO^-}$. They are both discussed here by computationally following the radiative association (RA) mechanism starting from $\mathrm{C_2^-}$, $\mathrm{H}$, $\mathrm{NC^-}$ and $\mathrm{O}$ as partners. The corresponding RA total cross sections produced by the calculations are in turn employed to generate the overall association rates over the relevant range of temperatures. The latter are found to be in line with other molecular ions formed by RA but not large enough to uniquivocally suggest this path as the main route to the anions formation in the ISM. Other possible paths of formation are also analysed and discussed. The presence of resonant structures during the association dynamics for both systems is found by the calculations and their consequences are discussed in some detail in the present study.