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Register a new userDetection of C5N- and vibrationally excited C6H in IRC +10216
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We report the detection in the envelope of the C-rich star IRC +10216 of four series of lines with harmonically related frequencies: B1389, B1390, B1394 and B1401. The four series must arise from linear molecules with mass and size close to those of C6H and C5N. Three of the series have half-integer rotational quantum numbers; we assign them to the 2Delta and 2Sigma vibronic states of C6H in its lowest (v_11) bending mode. The fourth series, B1389, has integer J with no evidence of fine or hyperfine structure; it has a rotational constant of 1388.860(2) MHz and a centrifugal distortion constant of 33(1) Hz; it is almost certainly the C5N- anion.
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Using the Submillimeter Array we have detected the J=3-2 and 2-1 rotational transitions from within the first vibrationally excited state of CO toward the extreme carbon star IRC+10216 (CW Leo). The emission remains spatially unresolved with an angular resolution of ~2 and, given that the lines originate from energy levels that are ~3100 K above the ground state, almost certainly originates from a much smaller (~10^{14} cm) sized region close to the stellar photosphere. Thermal excitation of the lines requires a gas density of ~10^{9} cm^{-3}, about an order of magnitude higher than the expected gas density based previous infrared observations and models of the inner dust shell of IRC+10216.
The J,K = 1,0-0,0 rotational transition of phosphine (PH3) at 267 GHz has been tentatively identified with a T_MB = 40 mK spectral line observed with the IRAM 30-m telescope in the C-star envelope IRC+10216. A radiative transfer model has been used to fit the observed line profile. The derived PH3 abundance relative to H2 is 6 x 10^(-9), although it may have a large uncertainty due to the lack of knowledge about the spatial distribution of this species. If our identification is correct, it implies that PH3 has a similar abundance to that reported for HCP in this source, and that these two molecules (HCP and PH3) together take up about 5 % of phosphorus in IRC+10216. The abundance of PH3, as that of other hydrides in this source, is not well explained by conventional gas phase LTE and non-LTE chemical models, and may imply formation on grain surfaces.
We present the detection of C4H2 for first time in the envelope of the C-rich AGB star IRC+10216 based on high spectral resolution mid-IR observations carried out with the Texas Echelon-cross-Echelle Spectrograph (TEXES) mounted on the Infrared Telescope Facility (IRTF). The obtained spectrum contains 24 narrow absorption features above the detection limit identified as lines of the ro-vibrational C4H2 band nu6+nu8(sigma_u^+). The analysis of these lines through a ro-vibrational diagram indicates that the column density of C4H2 is 2.4(1.5)E+16 cm^(-2). Diacetylene is distributed in two excitation populations accounting for 20 and 80% of the total column density and with rotational temperatures of 47(7) and 420(120) K, respectively. This two-folded rotational temperature suggests that the absorbing gas is located beyond ~0.4~20R* from the star with a noticeable cold contribution outwards from ~10~500R*. This outer shell matches up with the place where cyanoacetylenes and carbon chains are known to form due to the action of the Galactic dissociating radiation field on the neutral gas coming from the inner layers of the envelope.
Methyl formate in its first torsionally excited state (vt=1 at 131 cm-1) is detected for the first time toward W51 e2. All transitions from excited methyl formate within the observed spectral range are actually detected (82 transitions) and no strong lines are missing. The column density of the excited state is comparable to that of the ground state. For a source size of 7 we find that Trot = 104 +/- 14 K and N = 9.4 +4.0/-2.8 x 10^16 cm-2 for the excited state and Trot = 176 +/- 24 K and N = 1.7 +.2/-.2 x 10^17 cm-2 for the ground state. Lines from ethyl cyanide in its two first excited states (vt=1, torsion mode at 212 cm-1) and (vb=1, CCN in-plane bending mode at 206 cm-1) are also present in the observed spectrum. However blending problems prevent a precise estimate of its abundance. With regard to the number of lines of excited methyl formate and ethyl cyanide detected in W51 e2, it appears that excited states of large molecules certainly account for a large number of unidentified lines in spectral survey of molecular clouds.
A single dish monitoring of millimeter maser lines SiS J=14-13 and HCN nu_2 = 1^f J=3-2 and several other rotational lines is reported for the archetypal carbon star IRC+10216. Relative line strength variations of 5%~30% are found for eight molecular line features with respect to selected reference lines. Definite line-shape variation is found in limited velocity intervals of the SiS and HCN line profiles. The asymmetrical line profiles of the two lines are mainly due to the varying components. Their dominant varying components of the line profiles have similar periods and phases as the IR light variation, although both quantities show some degree of velocity dependence; there is also variability asymmetry between the blue and red line wings of both lines. Combining the velocities and amplitudes with a wind velocity model, we suggest that the line profile variations are due to SiS and HCN masing lines emanating from the wind acceleration zone. The possible link of the variabilities to thermal, dynamical and/or chemical processes within or under this region is also discussed.
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