Neutral–neutral reactions at the temperatures of interstellar clouds Rate coefficients for reactions of C2H radicals with O2, C2H2, C2H4 and C3H6 down to 15 K

1998 ◽  
Vol 109 ◽  
pp. 165-181 ◽  
Author(s):  
Delphine Chastaing ◽  
Philip L. James ◽  
Ian R. Sims ◽  
Ian W. M. Smith
1987 ◽  
Vol 120 ◽  
pp. 1-18
Author(s):  
Nigel G. Adams ◽  
David Smith

The current status of laboratory measurements of the rate coefficients for ionic reactions involved in interstellar molecular synthesis is discussed and the experimental techniques used to acquire such data are briefly described. Examples are given of laboratory data which are being obtained at temperatures close to those of interstellar clouds. Particular attention is given to the results of recent theoretical and experimental work which show that the rate coefficients for the binary reactions of ions with polar molecules at low temperatures are much larger than previously assumed. It is shown how these new developments in experiment and theory are reconciling the differences between predicted and observed abundances for some interstellar molecules. Also briefly discussed are: - the phenomenon of isotope exchange in ion/neutral reactions which explains the apparent enrichment of heavy isotopes in some interstellar molecules, the role of atoms in molecular synthesis, some studies of ion/neutral reactions pertaining to shocked regions of interstellar clouds, ternary association reactions and the analogous radiative association reactions, and recent new laboratory measurements of dissociative recombination coefficients. Finally, some guidance is offered in the proper choice of critical kinetic data for use in interstellar chemical modelling and some further requirements and likely future developments are mentioned.


1989 ◽  
Vol 8 ◽  
pp. 369-374 ◽  
Author(s):  
T. J. Millar

ABSTRACTChemical models of dense interstellar clouds are reviewed with particular emphasis on recent results. The need for theoretical and experimental data on rate coefficients is pointed out and some observational studies are suggested.


1997 ◽  
Vol 178 ◽  
pp. 539-542 ◽  
Author(s):  
E.F. Van Dishoeck

Astrochemistry makes enormous demands on laboratory and theoretical chemistry to obtain line frequencies, molecular parameters and rate coefficients for chemical reactions under interstellar conditions. The astrophysical needs for such large data bases continue to increase. For example, spectral line surveys at submillimeter wavelengths routinely contain thousands of rotational lines, whereas high resolution infrared and optical data require large amounts of information on vibrational and electronic transitions. The astrophysical modeling, both of interstellar clouds and of the envelopes and photospheres of stars, has improved to the stage that highly accurate molecular data are essential.


1987 ◽  
Vol 120 ◽  
pp. 295-296
Author(s):  
M. M. Graff ◽  
A. Dalgarno ◽  
A. F. Wagner

The internal energy distributions of reactants in shocked interstellar clouds are discussed. Rate coefficients appropriate for the oxygen chemistry of shocks differ significantly from those deduced by simple extrapolation of thermal measurements. A one-fluid MHD shock model examines nonthermal effects for a 10 km s−1 shock propagating through clouds of initial densities of 10 and 105 cm−3, using oxygen-hydrogen reaction rates that are specific to the vibrational, rotational, and fine structure temperatures of the reactants.


1987 ◽  
Vol 120 ◽  
pp. 235-244 ◽  
Author(s):  
Eric Herbst

Based on analyses by a variety of investigators, it has become understood that gas phase reactions can account for much of the chemistry observed in dense interstellar clouds. However, quantitative calculations of molecular abundances utilizing gas phase reactions are beset with difficulties. These difficulties include uncertainties in needed rate coefficients at the low temperatures of interstellar clouds, uncertainties in the dynamics of physical processes such as cloud collapse and clumping, and uncertainties in our understanding of gasgrain interactions. New work in some of these areas and its impact on modelling is emphasized.


2020 ◽  
Vol 638 ◽  
pp. A72
Author(s):  
François Lique ◽  
Alexandre Zanchet ◽  
Niyazi Bulut ◽  
Javier R. Goicoechea ◽  
Octavio Roncero

Context. SH+ is a surprisingly widespread molecular ion in diffuse interstellar clouds. There, it plays an important role by triggering the sulfur chemistry. In addition, SH+ emission lines have been detected at the UV-illuminated edges of dense molecular clouds, so-called photo-dissociation regions (PDRs), and toward high-mass protostars. An accurate determination of the SH+ abundance and of the physical conditions prevailing in these energetic environments relies on knowing the rate coefficients of inelastic collisions between SH+ molecules and hydrogen atoms, hydrogen molecules, and electrons. Aims. We derive SH+–H fine and hyperfine-resolved rate coefficients from recent quantum calculations for the SH+–H collisions, including inelastic, exchange, and reactive processes. Methods. The method we used is based on the infinite-order sudden approach. Results. State-to-state rate coefficients between the first 31 fine levels and 61 hyperfine levels of SH+ were obtained for temperatures ranging from 10 to 1000 K. Fine-structure resolved rate coefficients present a strong propensity rule in favor of Δj = ΔN transitions. The Δj = ΔF propensity rule is observed for the hyperfine transitions. Conclusions. The new rate coefficients will help significantly in the interpretation of SH+ spectra from PDRs and UV-irradiated shocks where the abundance of hydrogen atoms with respect to hydrogen molecules can be significant.


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