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S. Schlemmer

Publications and source records attributed to S. Schlemmer.

At least 19 recordsLinked to original sources

Space as a spectroscopic laboratory: High-resolution spectroscopy of the [$^{13}$C II] hyperfine structure with SOFIA/upGREAT

The [$^{12}$C II] emission at 158 $\mu$m is a key cooling line of the interstellar medium and traces gas kinematics in spectrally resolved observations. Its spectral profile is often modified by optical depth effects. The intrinsic line shape can be reconstructed by comparison with emission from the less abundant $^{13}$C isotope. Due to the additional neutron spin, [$^{13}$C II] emission splits into three hyperfine structure (hfs) transitions. Laboratory measurements have provided the centroid frequency and the strongest component ($F=2-1$); the two weaker components ($F=1-0$ and $F=1-1$) have been inferred only from quantum-mechanical calculations. The magnetic-dipole hfs constants, from which the transition frequencies follow, have not been measured experimentally. The high spectral resolution of observations with the upgraded German Receiver for Astronomy at Terahertz Frequencies (upGREAT) on board SOFIA enabled simultaneous detection of all three hfs transitions. From these astronomical data we determine, for the first time, the magnetic-dipole hfs constants $A_{1/2}^{\rm hf} = 810.71(11)$ MHz and $A_{3/2}^{\rm hf} = 162.18(5)$ MHz of the [$^{13}$C II] $2s^2\,2p\,{}^2P^\circ$ ground term. Combined with the laboratory centroid frequency, this yields the rest frequencies of all three hfs lines. Using [$^{12}$C II] as a reference, we also improve the precision of the [$^{13}$C II] centroid frequency. This work shows that spectrally resolved astronomical observations can constrain fundamental atomic properties, with hfs precision rivaling laboratory measurements. The approach extends to other atomic and molecular transitions where laboratory data are difficult to obtain.

astro-ph.GA

Rotational spectroscopy of CH$_3$OD with a reanalysis of CH$_3$OD toward IRAS 16293$-$2422

We have started a measurement campaign of numerous methanol isotopologs in low-lying torsional states in order to provide extensive line lists for radio astronomical observations from an adequate spectroscopic model and to investigate how the intricate vibration-torsion-rotation interactions manifest themselves in the spectra of different isotopic species. After CD$_3$OH and CD$_3$OD, we turn our focus to CH$_3$OD, which is an important species for studying deuteration in prestellar cores and envelopes that enshroud protostars. Notably, deuteration is frequently viewed as a diagnostic tool for star formation. The measurements used in this study were obtained in two spectroscopic laboratories and cover large fractions of the 34 GHz--1.35 THz range. As done in previous studies, we employed a torsion-rotation Hamiltonian model for our analysis that is based on the rho-axis method. The resulting model describes the ground and first excited torsional states of CH$_3$OD well up to quantum numbers $J \leqslant 51$ and $K_a \leqslant 18$. We derived a line list for radio astronomical observations from this model that is accurate up to at least 1.35~THz and should be sufficient for all types of radio astronomical searches for this methanol isotopolog in these two lowest torsional states. This line list was applied to a reinvestigation of CH$_3$OD in data from the Protostellar Interferometric Line Survey of IRAS 16293--2422 obtained with the Atacama Large Millimeter/submillimeter Array. The new accurately determined value for the column density of CH$_3$OD implies that the deuteration in methanol differs in its two functional groups by a factor of $\sim$7.5.

astro-ph.GA

Investigation of the rotational spectrum of CD$_3$OD and an astronomical search toward IRAS 16293$-$2422

Solar-type prestellar cores and protostars display large amounts of deuterated organic molecules. Recent findings on CHD$_2$OH and CD$_3$OH toward IRAS 16293-2422 suggest that even fully deuterated methanol, CD$_3$OD, may be detectable as well. However, searches for CD$_3$OD are hampered in particular by the lack of intensity information from a spectroscopic model. The objective of the present investigation is to develop a spectroscopic model of CD$_3$OD in low-lying torsional states that is sufficiently accurate to facilitate searches for this isotopolog in space. We carried out a new measurement campaign for CD$_3$OD involving two spectroscopic laboratories that covers the 34 GHz-1.1 THz range. A torsion-rotation Hamiltonian model based on the rho-axis method was employed for our analysis. Our resulting model describes the ground and first excited torsional states of CD$_3$OD well up to quantum numbers $J \leq 51$ and $K_a \leq 23$. We derived a line list for radio-astronomical observations from this model that is accurate up to at least 1.1 THz and should be sufficient for all types of radio-astronomical searches for this methanol isotopolog. This line list was used to search for CD$_3$OD in data from the Protostellar Interferometric Line Survey of IRAS 16293$-$2422 obtained with the Atacama Large Millimeter/submillimeter Array. While we found several emission features that can be attributed largely to CD$_3$OD, their number is still not sufficiently high enough to establish a clear detection. Nevertheless, the estimate of 2$\times 10^{15}$ cm$^{-2}$ derived for the CD$_3$OD column density may be viewed as an upper limit that can be compared to column densities of CD$_3$OH, CH$_3$OD, and CH$_3$OH. The comparison indicates that the CD$_3$OD column density toward IRAS 16293-2422 is in line with the enhanced D/H ratios observed for multiply deuterated complex organic molecules.

astro-ph.SR

Discovery of H$_2$CCCH$^+$ in TMC-1

Based on a novel laboratory method, 14 mm-wave lines of the molecular ion H$_2$CCCH$^+$ have been measured in high resolution, and the spectroscopic constants of this asymmetric rotor determined with high accuracy. Using the Yebes 40 m and IRAM 30 m radio telescopes, we detect four lines of H$_2$CCCH$^+$ towards the cold dense core TMC-1. With a dipole moment of about 0.55 Debye obtained from high-level ab initio calculations, we derive a column density of 5.4$\pm$1$\times$10$^{11}$ cm$^{-2}$ and 1.6$\pm$0.5$\times$10$^{11}$ cm$^{-2}$ for the ortho and para species, respectively, and an abundance ratio N(H$_2$CCC)/N(H$_2$CCCH$^+$)= 2.8$\pm$0.7. The chemistry of H$_2$CCCH$^+$ is modelled using the most recent chemical network for the reactions involving the formation of H$_2$CCCH$^+$. We find a reasonable agreement between model predictions and observations, and new insights into the chemistry of C$_3$ bearing species in TMC-1 are obtained.

astro-ph.GA

Rotation-tunneling spectrum and astrochemical modeling of dimethylamine, CH$_3$NHCH$_3$, and searches for it in space

Methylamine has been the only simple alkylamine detected in the interstellar medium for a long time. With the recent secure and tentative detections of vinylamine and ethylamine, respectively, dimethylamine has become a promising target for searches in space. Its rotational spectrum, however, has been known only up to 45 GHz until now. Here we investigate the rotation-tunneling spectrum of dimethylamine in selected regions between 76 and 1091 GHz using three different spectrometers in order to facilitate its detection in space. The quantum number range is extended to $J = 61$ and $K_a = 21$, yielding an extensive set of accurate spectroscopic parameters. To search for dimethylamine, we refer to the spectral line survey ReMoCA carried out with the Atacama Large Millimeter/submillimeter Array toward the high-mass star-forming region Sagittarius B2(N) and a spectral line survey of the molecular cloud G+0.693$-$0.027 employing the IRAM 30 m and Yebes 40 m radio telescopes. We report nondetections of dimethylamine toward the hot molecular cores Sgr B2(N1S) and Sgr B2(N2b) as well as G+0.693$-$0.027 which imply that dimethylamine is at least 14, 4.5 and 39 times less abundant than methylamine toward these sources, respectively. The observational results are compared to computational results from a gas-grain astrochemical model. The modeled methylamine to dimethylamine ratios are compatible with the observational lower limits. However, the model produces too much ethylamine compared with methylamine which could mean that the already fairly low levels of dimethylamine in the models may also be too high.

astro-ph.GA

Rotational spectroscopy $n$-propanol: $Aa$ and $Ag$ conformers

The primary alcohol $n$-propanol (i.e., $normal$-propanol or propan-1-ol; C$_3$H$_7$OH) occurs in five different conformers: $Ga$, $Gg$, $Gg'$, $Aa$, and $Ag$. All rotational spectra of the three conformers of the $G$ family are well described, making astronomical search of their spectroscopic signatures possible, as opposed to those of the $Aa$ and $Ag$ conformers. Our goal is to facilitate the astronomical detection of $Aa$ and $Ag$ conformers of $n$-propanol by characterizing their rotational spectra. We recorded the rotational spectra of $n$-propanol in the frequency domain of 18$-$505\,GHz.Additional double-modulation double-resonance (DM-DR) measurements were performed, more specifically with the goal to unambiguously assign weak transitions of the $Aa$ conformer and to verify assignments of the $Ag$ conformer. We derived a spectroscopic quantum mechanical model with experimental accuracy (with $J_\textrm{max}=70$ and $K_{a,\textrm{max}}=6$) for $Aa$ $n$-propanol. Furthermore, we unambiguously assigned transitions (with $J_\textrm{max}=69$ and $K_{a,\textrm{max}}=9$) of $Ag$ $n$-propanol; in doing so, we prove the existence of two tunneling states, $Ag^+$ and $Ag^-$. The astronomical search of all five conformers of $n$-propanol is now possible via their rotational signatures. These are applied in a companion article on the detection of $n$-propanol toward the hot molecular core Sgr B2(N2).

physics.chem-ph

Rotational and rovibrational spectroscopy of CD$_3$OH with an account of CD$_3$OH toward IRAS 16293$-$2422

Solar-type protostars harbor highly deuterated complex organics. While this degree of deuteration may provide important clues in studying the formation of these species, spectroscopic information on multiply deuterated isotopologs is often insufficient. In particular, searches for triply deuterated methanol, CD$_3$OH, are hampered by the lack of intensity information from a spectroscopic model. The aim of the present study is to develop such a model of CD$_3$OH in low-lying torsional states that is sufficiently accurate to facilitate further searches for CD$_3$OH in space. We performed a new measurement campaign for CD$_3$OH involving three spectroscopic laboratories that covers the 34 GHz-1.1 THz and the 20-900 cm$^{-1}$ ranges. The analysis was performed using the torsion-rotation Hamiltonian model based on the rho-axis method. We determined a model that describes the ground and first excited torsional states of CD$_3$OH, up to quantum numbers $J \leqslant 55$ and $K_a \leqslant 23$, and we derived a line list for radio-astronomical observations. This list is accurate up to at least 1.1 THz and should be sufficient for all types of radio-astronomical searches for this methanol isotopolog. It was used to search for CD$_3$OH in data from the Protostellar Interferometric Line Survey of IRAS 16293-2422 using ALMA. CD$_3$OH is securely detected in the data, with a large number of clearly separated and well-reproduced lines. We detected lines belonging to the ground and the first excited torsional states. The derived abundance of CD$_3$OH relative to non-deuterated isotopolog confirm the significant enhancement of this multiply deuterated variant. This finding is in line with other observations of multiply deuterated complex organic molecules and may serve as an important constraint on their formation models.

astro-ph.GA

Millimeter-wave spectroscopy of the $^{13}$CH$_3$OD isotopic species of methyl alcohol

The dramatic increase in sensitivity, spectral coverage and resolution of radio astronomical facilities in recent years has opened new possibilities for observation of chemical differentiation and isotopic fractionation in protostellar sources to shed light on their spatial and temporal evolution. In warm interstellar environments, methanol is an abundant species, hence spectral data for its isotopic forms are of special interest. In the present work, the millimeter-wave spectrum of the $^{13}$CH$_3$OD isotopologue has been investigated over the region from 150$-$510 GHz to provide a set of transition frequencies for potential astronomical application. The focus is on two types of prominent $^{13}$CH$_3$OD spectral groupings, namely the $a$-type $^qR$-branch multiplets and the $b$-type $Q$-branches. Line positions are reported for the $^qR(J)$ clusters for $J = 3$ to 10 for the $v_{\rm t} = 0$ and 1 torsional states, and for a number of $v_{\rm t} = 0$ and 1 $^rQ(J)$ or $^pQ(J)$ line series up to $J = 25$. The frequencies have been fitted to a multi-parameter torsion-rotation Hamiltonian, and upper level excitation energies have been calculated from the resulting molecular constants.

astro-ph.IM

Descendant of the X-ogen carrier and a "mass of 69": Infrared action spectroscopic detection of HC$_3$O$^+$ and HC$_3$S$^+$

The carbon chain ions HC$_3$O$^+$ and HC$_3$S$^+$ - longer variants of the famous "X-ogen" line carrier HCO$^+$ - have been observed for the first time using two cryogenic 22-pole ion trap apparatus (FELion, Coltrap) and two different light sources: the Free Electron Laser for Infrared eXperiments (FELIX), which was operated between 500 and 2500 cm$^{-1}$ and an optical parametric oscillator operating near 3200 cm$^{-1}$; signals from both experiments were detected by infrared predissociation action spectroscopy. The majority of vibrational fundamentals were observed for both ions and their vibrational wavenumbers compare very favorably with results from high-level anharmonic force field calculations performed here at the coupled-cluster level of theory. As the action spectroscopic scheme probes the Ne-tagged weakly bound variants, Ne$-$HC$_3$O$^+$ and Ne$-$HC$_3$S$^+$, corresponding calculations of these systems were also performed. Differences in the structures and molecular force fields between the bare ions and their Ne-tagged complexes are found to be very small.

physics.chem-ph

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.

astro-ph.SR

Rotational spectroscopy of methyl mercaptan CH$_3$$^{32}$SH at millimeter and submillimeter wavelengths

We present a new global study of the millimeter (mm) wave, submillimeter (sub-mm) wave, and terahertz (THz) spectra of the lowest three torsional states of methyl mercaptan (CH$_3$SH). New measurements have been carried out between 50 and 510 GHz using the Kharkiv mm wave and the Cologne sub-mm wave spectrometers whereas THz spectra records were used from our previous study. The new data, involving torsion-rotation transitions with $J$ up to 61 and $K_a$ up to 18, were combined with previously published measurements and fit using the rho-axis-method torsion-rotation Hamiltonian. The final fit used 124 parameters to give an overall weighted root-mean-square deviation of 0.72 for the dataset consisting of 6965 microwave (MW) and 16345 far-infrared line frequencies sampling transitions within and between the ground, first, and second excited torsional states. This investigation presents a two-fold expansion in the $J$ quantum numbers and a significant improvement in the fit quality, especially for the MW part of the data, thus allowing us to provide more reliable predictions to support astronomical observations.

astro-ph.IM

Laboratory spectroscopic study of isotopic thioformaldehyde, H$_{2}$CS, and determination of its equilibrium structure

Thioformaldehyde is an abundant molecule in various regions of the interstellar medium. However, available laboratory data limit the accuracies of calculated transition frequencies in the submillimeter region, in particular for minor isotopic species. We aim to determine spectroscopic parameters of isotopologs of H2CS that are accurate enough for predictions well into the submillimeter region. We investigated the laboratory rotational spectra of numerous isotopic species in natural isotopic composition almost continuously between 110 and 377 GHz. Individual lines were studied for most species in two frequency regions between 566 and 930 GHz. Further data were obtained for the three most abundant species in the 1290-1390 GHz region. New or improved spectroscopic parameters were determined for seven isotopic species. Quantum-chemical calculations were carried out to evaluate the differences between ground state and equilibrium rotational parameters to derive semi-empirical equilibrium structural parameters. The spectroscopic parameters are accurate enough for predictions well above 1 THz with the exception of H2(13)C(34)S where the predictions should be reliable to around 700 GHz.

astro-ph.SR

Laboratory spectroscopic study of the $^{15}$N isotopomers of cyanamide, H$_2$NCN, and a search for them toward IRAS 16293$-$2422 B

Cyanamide is one of the few interstellar molecules containing two chemically different N atoms. It was detected recently toward the solar-type protostar IRAS 16293-2422 B together with H$_2$N$^{13}$CN and HDNCN in the course of the Atacama Large Millemeter/submillimeter Array (ALMA) Protostellar Interferometric Line Survey (PILS). The detection of the 15N isotopomers or the determination of upper limits to their column densities was hampered by the lack of accurate laboratory data at the frequencies of the survey. We wanted to determine spectroscopic parameters of the $^{15}$N isotopomers of cyanamide that are accurate enough for predictions well into the submillimeter region and to search for them in the PILS data. We investigated the laboratory rotational spectra of H$_2^{15}$NCN and H$_2$NC$^{15}$N in the selected region between 192 and 507~GHz employing a cyanamide sample in natural isotopic composition. Additionally, we recorded transitions of H$_2$N$^{13}$CN. We obtained new or improved spectroscopic parameters for the three isotopic species. Neither of the $^{15}$N isotopomers of cyanamide were detected unambiguously in the PILS data. Two relatively clean lines can be tentatively assigned to H$_2^{15}$NCN. If confirmed, their column densities would imply a low $^{14}$N/$^{15}$N ratio for cyanamide toward this source. The resulting line lists should be accurate enough for observations up to about 1 THz. More sensitive observations, potentially at different frequencies, may eventually lead to the astronomical detection of these isotopic species.

astro-ph.SR

The CO-H2 van der Waals complex and complex organic molecules in cold molecular clouds: a TMC-1C survey

Almost 200 different species have been detected in the interstellar medium (ISM) during the last decades, revealing not only simple species but complex molecules with more than 6 atoms. Other exotic compounds, like the weakly-bound dimer (H2)2, have also been detected in astronomical sources like Jupiter. We aim at detecting for the first time the CO-H2 van der Waals complex in the ISM, which if detected can be a sensitive indicator for low temperatures. We use the IRAM30m telescope, located in Pico Veleta (Spain), to search for the CO-H2 complex in a cold, dense core in TMC-1C (with a temperature of 10 K). All the brightest CO-H2 transitions in the 3 mm (80-110 GHz) band have been observed with a spectral resolution of 0.5-0.7 km/s, reaching a rms noise level of 2 mK. The simultaneous observation of a broad frequency band, 16 GHz, has allowed us to conduct a serendipitous spectral line survey. No lines belonging to the CO-H2 complex have been detected. We have set up a new, more stringent upper limit for its abundance to be [CO-H2]/[CO] = 5x10^{-6}, while we expect the abundance of the complex to be in the range 10^{-8}-10^{-3}. The spectral line survey has allowed us to detect 75 lines associated with 41 different species (including isotopologues). We detect a number of complex organic species, e.g. methyl cyanide (CH3CN), methanol (CH3OH), propyne (CH3CCH) and ketene (CH2CO), associated with cold gas (excitation temperatures about 7 K), confirming the presence of these complex species not only in warm objects but also in cold regimes.

astro-ph.GA

Exploring molecular complexity with ALMA (EMoCA): Alkanethiols and alkanols in Sagittarius B2(N2)

Over the past five decades, radio astronomy has shown that molecular complexity is a natural outcome of interstellar chemistry, in particular in star forming regions. However, the pathways that lead to the formation of complex molecules are not completely understood and the depth of chemical complexity has not been entirely revealed. In addition, the sulfur chemistry in the dense interstellar medium is not well understood. We want to know the relative abundances of alkanethiols and alkanols in the Galactic Center source Sagittarius B2(N2), the northern hot molecular core in Sgr B2(N), whose relatively small line widths are favorable for studying the molecular complexity in space. We investigated spectroscopic parameter sets that were able to reproduce published laboratory rotational spectra of ethanethiol and studied effects that modify intensities in the predicted rotational spectrum of ethanol. We used the Atacama Large Millimeter Array (ALMA) in its Cycles~0 and 1 for a spectral line survey of Sagittarius B2(N) between 84 and 114.4 GHz. These data were analyzed by assuming local thermodynamic equilibrium (LTE) for each molecule. Our observations are supplemented by astrochemical modeling; a new network is used for the first time that includes reaction pathways for alkanethiols. The column density ratios involving methanol, ethanol, and methanethiol in Sgr B2(N2) are similar to values reported for Orion KL, but those involving ethanethiol are significantly different and suggest that the detection of ethanethiol reported toward Orion KL is uncertain. Our chemical model presently does not permit the prediction of sufficiently accurate column densities of alkanethiols or their ratios among alkanethiols and alkanols. Therefore, additional observational results are required to establish the level of C2H5SH in the dense and warm interstellar medium with certainty.

astro-ph.GA

A study of the C$_3$H$_2$ isomers and isotopologues: first interstellar detection of HDCCC

The partially deuterated linear isomer HDCCC of the ubiquitous cyclic carbene ($c$-C$_3$H$_2$) was observed in the starless cores TMC-1C and L1544 at 96.9 GHz, and a confirming line was observed in TMC-1 at 19.38 GHz. To aid the identification in these narrow line sources, four centimetre-wave rotational transitions (two in the previously reported $K_a =0$ ladder, and two new ones in the $K_a =1$ ladder), and 23 transitions in the millimetre band between 96 and 272 GHz were measured in high-resolution laboratory spectra. Nine spectroscopic constants in a standard asymmetric top Hamiltonian allow the principal transitions of astronomical interest in the $K_a \le 3$ rotational ladders to be calculated to within 0.1 km s$^{-1}$ in radial velocity up to 400 GHz. Conclusive evidence for the identification of the two astronomical lines of HDCCC was provided by the $V_{\rm{LSR}}$ which is the same as that of the normal isotopic species (H$_2$CCC) in the three narrow line sources. In these sources, deuterium fractionation in singly substituted H$_2$CCC (HDCCC/H$_2$CCC $\sim4\%\text{-}19\%$) is comparable to that in $c$-C$_3$H$_2$ ($c$-C$_3$H$_2$/$c$-C$_3$HD $\sim5\%\text{-}17\%$), and similarly in doubly deuterated $c$-C$_3$H$_2$ ($c$-C$_3$D$_2$/$c$-C$_3$HD $\sim3\%\text{-}17\%$), implying that the efficiency of the deuteration processes in the H$_2$CCC and $c$-C$_3$H$_2$ isomers are comparable in dark clouds.

astro-ph.GA

Spin-state chemistry of deuterated ammonia

Aims. We aim to develop a chemical model that contains a consistent description of spin-state chemistry in reactions involving chemical species with multiple deuterons. We apply the model to the specific case of deuterated ammonia, to derive values for the various spin-state ratios. Methods. We apply symmetry rules in the complete scrambling assumption to calculate branching ratio tables for reactions between chemical species that include multiple protons and/or deuterons. Reaction sets for both gas-phase and grain-surface chemistry are generated using an automated routine that forms all possible spin-state variants of any given reaction with up to six H/D atoms. Single-point and modified Bonnor-Ebert models are used to study the density and temperature dependence of ammonia and its isotopologs, and the associated spin-state ratios. Results. We find that the spin-state ratios of the ammonia isotopologs are, at late times, very different from their statistical values. The ratios are rather insensitive to variations in the density, but present strong temperature dependence. We derive high peak values ($\sim$ 0.1) for the deuterium fraction in ammonia, in agreement with previous (gas-phase) models. The deuterium fractionation is strongest at high density, corresponding to a high degree of depletion, and also presents temperature dependence. We find that in the temperature range 5 to 20 K, the deuterium fractionation peaks at $\sim$ 15 K while most of the ortho/para (and meta/para for $\rm ND_3$) ratios present a minimum at 10 K (ortho/para $\rm NH_2D$ has instead a maximum at this temperature). Conclusions. Owing to the density and temperature dependence found in the abundances and spin-state ratios of ammonia and its isotopologs, it is evident that observations of ammonia and its deuterated forms can provide important constraints on the physical structure of molecular clouds.

astro-ph.GA

The 2014 KIDA network for interstellar chemistry

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.

astro-ph.GA