No Arabic abstract
We report the first sub-arc second (0.65$arcsec$ $times$ 0.51$arcsec$) image of the dimethyl ether molecule, (CH$_{3}$)$_{2}$O, toward the Orion Kleinmann-Low nebula (Orion--KL). The observations were carried at 43.4 GHz with the Expanded Very Large Array (EVLA). The distribution of the lower energy transition 6$_{1,5} - 6_{0,6}$, EE (E$rm_{u}$ = 21 K) mapped in this study is in excellent agreement with the published dimethyl ether emission maps imaged with a lower resolution. The main emission peaks are observed toward the Compact Ridge and Hot Core southwest components, at the northern parts of the Compact Ridge and in an intermediate position between the Compact Ridge and the Hot Core. A notable result is that the distribution of dimethyl ether is very similar to that of another important larger O-bearing species, the methyl formate (HCOOCH$_{3}$), imaged at lower resolution. Our study shows that higher spectral resolution (WIDAR correlator) and increased spectral coverage provided by the EVLA offer new possibilities for imaging complex molecular species. The sensitivity improvement and the other EVLA improvements make this instrument well suited for high sensitivity, high angular resolution, molecular line imaging.
We report on the tentative detection of $trans$ Ethyl Methyl Ether (tEME), $t-CH_3CH_2OCH_3$, through the identification of a large number of rotational lines from each one of the spin states of the molecule towards Orion KL. We also search for $gauche$-$trans$-n-propanol, $Gt-n-CH_3CH_2CH_2OH$, an isomer of tEME in the same source. We have identified lines of both species in the IRAM 30m line survey and in the ALMA Science Verification data. We have obtained ALMA maps to establish the spatial distribution of these species. Whereas tEME mainly arises from the compact ridge component of Orion, Gt-n-propanol appears at the emission peak of ethanol (south hot core). The derived column densities of these species at the location of their emission peaks are $leq(4.0pm0.8)times10^{15} cm^{-2}$ and $leq(1.0pm0.2)times10^{15} cm^{-2}$ for tEME and Gt-n-propanol, respectively. The rotational temperature is $sim100 K$ for both molecules. We also provide maps of $CH_3OCOH$, $CH_3CH_2OCOH$, $CH_3OCH_3$, $CH_3OH$, and $CH_3CH_2OH$ to compare the distribution of these organic saturated O-bearing species containing methyl and ethyl groups in this region. Abundance ratios of related species and upper limits to the abundances of non-detected ethers are provided. We derive an abundance ratio $N(CH_3OCH_3)/N(tEME)geq150$ in the compact ridge of Orion.
Recent interferometric observations have called into question the traditional view of the Orion-KL region, which displays one of the most well-defined cases of chemical differentiation in a star-forming region. Previous, lower-resolution images of Orion-KL show emission signatures for oxygen-bearing organic molecules toward the Orion Compact Ridge, and emission for nitrogen-bearing organic molecules toward the Orion Hot Core. However, more recent observations at higher spatial resolution indicate that the bulk of the molecular emission is arising from many smaller, compact clumps that are spatially distinct from the traditional Hot Core and Compact Ridge sources. It is this type of observational information that is critical for guiding astrochemical models, as the spatial distribution of molecules and their relation to energetic sources will govern the chemical mechanisms at play in star-forming regions. We have conducted millimeter imaging studies of Orion-KL with various beam sizes using CARMA in order to investigate the continuum structure. These lambda;=3mm observations have synthesized beam sizes of ~0.5-5.0. These observations reveal the complex continuum structure of this region, which stands in sharp contrast to the previous structural models assumed for Orion-KL based on lower spatial resolution images. The new results indicate that the spatial scaling previously used in determination of molecular abundances for this region are in need of complete revision. Here we present the results of the continuum observations, discuss the sizes and structures of the detected sources, and suggest an observational strategy for determining the proper spatial scaling to accurately determine molecular abundances in the Orion-KL region.
The torsional Raman spectra of two astrophysically detected isotopologues of dimethyl-ether, ($^{12}$CH$_3$O$^{12}$CH$_3$ and $^{13}$CH$_3$O$^{12}$CH$_3$), have been recorded at room temperature and cooled in supersonic jet, and interpreted with the help of highly correlated ab initio calculations. Dimethyl-ether displays excited torsional and vibrational levels at low energy that can be populated at the temperatures of the star forming regions, obliging to extend the analysis of the rotational spectrum over the ground state. Its spectrum in the THz region is rather complex due to the coupling of the torsional overtones $2 u_{11}$ and $2 u_{15}$ with the COC bending mode, and the presence of many hot bands. The torsional overtones are set here at $2 u_{11}=385.2$~cm$^{-1}$ and $2 u_{15}=482.0$~cm$^{-1}$ for $^{12}$CH$_3$O$^{12}$CH$_3$, and $2 u_{11}=385.0$~cm$^{-1}$ and $2 u_{15}=481.1$~cm$^{-1}$ for $^{13}$CH$_3$O$^{12}$CH$_3$. The new assignment of $2 u_{11}$ is downshifted around $sim 10$~cm$^{-1}$ with respect to the literature. All the other (hot) bands have been re-assigned consistently. In addition, the infrared-forbidden torsional fundamental band $ u_{11}$ is observed here at 197.8~cm$^{-1}$. The new spectral characterization in the THz region reported here provides improved values of the Hamiltonian parameters, to be used in the analysis of the rotational spectra of DME isotopologues for further astrophysical detections.
Complex organic molecules (COMs) have been detected in a variety of interstellar sources. The abundances of these COMs in warming sources can be explained by syntheses linked to increasing temperatures and densities, allowing quasi-thermal chemical reactions to occur rapidly enough to produce observable amounts of COMs, both in the gas phase, and upon dust grain ice mantles. The COMs produced on grains then become gaseous as the temperature increases sufficiently to allow their thermal desorption. The recent observation of gaseous COMs in cold sources has not been fully explained by these gas-phase and dust grain production routes. Radiolysis chemistry is a possible non-thermal method of producing COMs in cold dark clouds. This new method greatly increases the modeled abundance of selected COMs upon the ice surface and within the ice mantle due to excitation and ionization events from cosmic ray bombardment. We examine the effect of radiolysis on three C$_{2}$H$_{4}$O$_{2}$ isomers -- methyl formate (HCOOCH$_3$), glycolaldehyde (HCOCH$_2$OH), and acetic acid (CH$_3$COOH) -- and a chemically similar molecule, dimethyl ether (CH$_3$OCH$_3$), in cold dark clouds. We then compare our modelled gaseous abundances with observed abundances in TMC-1, L1689B, and B1-b.
The CH$^+$ ion is a key species in the initial steps of interstellar carbon chemistry. Its formation in diverse environments where it is observed is not well understood, however, because the main production pathway is so endothermic (4280 K) that it is unlikely to proceed at the typical temperatures of molecular clouds. We investigation CH$^+$ formation with the first velocity-resolved spectral mapping of the CH$^+$ $J=1-0, 2-1$ rotational transitions, three sets of CH $Lambda$-doubled triplet lines, $^{12}$C$^+$ and $^{13}$C$^+$, and CH$_3$OH 835~GHz E-symmetry Q branch transitions, obtained with Herschel/HIFI over $approx$12 arcmin$^2$ centered on the Orion BN/KL source. We present the spatial morphologies and kinematics, cloud boundary conditions, excitation temperatures, column densities, and $^{12}$C$^+$ optical depths. Emission from C$^+$, CH$^+$, and CH is indicated to arise in the diluted gas, outside of the explosive, dense BN/KL outflow. Our models show that UV-irradiation provides favorable conditions for steady-state production of CH$^+$ in this environment. Surprisingly, no spatial or kinematic correspondences of these species are found with H$_2$ S(1) emission tracing shocked gas in the outflow. We propose that C$^+$ is being consumed by rapid production of CO to explain the lack of C$^+$ and CH$^+$ in the outflow, and that fluorescence provides the reservoir of H$_2$ excited to higher ro-vibrational and rotational levels. Hence, in star-forming environments containing sources of shocks and strong UV radiation, a description of CH$^+$ formation and excitation conditions is incomplete without including the important --- possibly dominant --- role of UV irradiation.