No Arabic abstract
We report the discovery of propylene (also called propene, CH_2CHCH_3) with the IRAM 30-m radio telescope toward the dark cloud TMC-1. Propylene is the most saturated hydrocarbon ever detected in space through radio astronomical techniques. In spite of its weak dipole moment, 6 doublets (A and E species) plus another line from the A species have been observed with main beam temperatures above 20 mK. The derived total column density of propylene is 4 10^13 cm^-2, which corresponds to an abundance relative to H_2 of 4 10^-9, i.e., comparable to that of other well known and abundant hydrocarbons in this cloud, such as c-C_3H_2. Although this isomer of C_3H_6 could play an important role in interstellar chemistry, it has been ignored by previous chemical models of dark clouds as there seems to be no obvious formation pathway in gas phase. The discovery of this species in a dark cloud indicates that a thorough analysis of the completeness of gas phase chemistry has to be done.
Life on Earth relies on chiral molecules, that is, species not superimposable on their mirror images. This manifests itself in the selection of a single molecular handedness, or homochirality, across the biosphere. We present the astronomical detection of a chiral molecule, propylene oxide (CH$_3$CHCH$_2$O), in absorption toward the Galactic Center. Propylene oxide is detected in the gas phase in a cold, extended molecular shell around the embedded, massive protostellar clusters in the Sagittarius B2 star-forming region. This material is representative of the earliest stage of solar system evolution in which a chiral molecule has been found.
Networks of reactions on dust grain surfaces play a crucial role in the chemistry of interstellar clouds, leading to the formation of molecular hydrogen in diffuse clouds as well as various organic molecules in dense molecular clouds. Due to the sub-micron size of the grains and the low flux, the population of reactive species per grain may be very small and strongly fluctuating. Under these conditions rate equations fail and the simulation of surface-reaction networks requires stochastic methods such as the master equation. However, the master equation becomes infeasible for complex networks because the number of equations proliferates exponentially. Here we introduce a method based on moment equations for the simulation of reaction networks on small grains. The number of equations is reduced to just one equation per reactive specie and one equation per reaction. Nevertheless, the method provides accurate results, which are in excellent agreement with the master equation. The method is demonstrated for the methanol network which has been recently shown to be of crucial importance.
We discuss the first astronomical detection of the CF+ (fluoromethylidynium) ion, obtained by observations of the J=1-0 (102.6 GHz), J=2-1 (205.2 GHz) and J=3-2 (307.7 GHz) rotational transitions toward the Orion Bar region. Our search for CF+, carried out using the IRAM 30m and APEX 12m telescopes, was motivated by recent theoretical models that predict CF+ abundances of a few times 1.E-10 in UV-irradiated molecular regions where C+ is present. The CF+ ion is produced by exothermic reactions of C+ with HF. Because fluorine atoms can react exothermically with H2, HF is predicted to be the dominant reservoir of fluorine, not only in well-shielded regions but also in the surface layers of molecular clouds where the C+ abundance is large. The observed CF+ line intensities imply the presence of CF+ column densities of at least 1.E+12 cm-2 over a region of size at least ~ 1 arcmin, in good agreement with theoretical predictions. They provide support for our current theories of interstellar fluorine chemistry, which suggest that hydrogen fluoride should be ubiquitous in interstellar gas clouds and widely detectable in absorption by future satellite and airborne observatories.
Chemical models used to study the chemical composition of the gas and the ices in the interstellar medium are based on a network of chemical reactions and associated rate coefficients. These reactions and rate coefficients are partially compiled from data in the literature, when available. We present in this paper kida.uva.2014, a new updated version of the kida.uva public gas-phase network first released in 2012. In addition to a description of the many specific updates, we illustrate changes in the predicted abundances of molecules for cold dense cloud conditions as compared with the results of the previous version of our network, kida.uva.2011.
We report the detection of linear and cyclic isomers of C3H and C3H2 towards various starless cores and review the corresponding chemical pathways involving neutral (C3Hx with x=1,2) and ionic (C3Hx+ with x = 1,2,3) isomers. We highlight the role of the branching ratio of electronic Dissociative Recombination (DR) reactions of C3H2+ and C3H3+ isomers showing that the statistical treatment of the relaxation of C3H* and C3H2* produced in these DR reactions may explain the relative c,l-C3H and c,l-C3H2 abundances. We have also introduced in the model the third isomer of C3H2 (HCCCH). The observed cyclic-to-linear C3H2 ratio vary from 110 + or - 30 for molecular clouds with a total density around 1e4 molecules.cm-3 to 30 + or - 10 for molecular clouds with a total density around 4e5 molecules.cm-3, a trend well reproduced with our updated model. The higher ratio for low molecular cloud densities is mainly determined by the importance of the H + l-C3H2 -> H + c-C3H2 and H + t-C3H2 -> H + c-C3H2 isomerization reactions.