Far-infrared spectrum of excited torsional states of C-13 methanol

The torsion-rotation structure of the far-infrared (FIR) spectrum of the C-13 isotopic species of methyl alcohol has been investigated by high-resolution Fourier transform spectroscopy in the 25–350 cm^–1 region, with emphasis on subbands involving excited torsional states. In this study, 89 such subbands have been identified, with torsional states fromn=1 ton=3 included. As well, a further 4 assignments have been added to our previous work on then=0 ground torsional state. The subband origins together with known microwave results have been fitted by least-squares to our torsion-rotation Hamiltonian, and improved molecular structural and torsional constants for the vibrational ground state are reported. Tables of state-specific constants representing the three leading terms in aJ(J+1) power-series expansion of the torsion-rotation energy levels are given for torsional statesn=0 to 3 and rotationalK values from 0 to 16.     

Torsion-rotation global analysis and database for the CH3OH isotopomer of methanol

Fourier-transform far-infrared spectra of CH₃¹⁸OH in the 15-470 cm⁻¹ region have been analyzed by means of the Ritz assignment program. The far-infrared data have been combined with the literature microwave and millimeter-wave measurements in a full global fitting of the first three torsional states (ν_t = 0, 1, and 2) of the CH₃¹⁸OH ground vibrational state. The fitted dataset includes 550 microwave and millimeter-wave lines and more than 17 000 Fourier-transform transitions covering the quantum number ranges J ? 30, K ? 15, and ν_t ? 2. With incorporation of 79 adjustable parameters, the global fit achieved convergence with an overall weighted standard deviation of 1.072, essentially to within the assigned measurement uncertainties of ±50 kHz for almost all of the microwave and millimeter-wave lines and ±6 MHz (0.0002 cm⁻¹) to ±15 MHz (0.0005 cm⁻¹) for the Fourier-transform far-infrared measurements. Based on the global fit results, a database has been compiled containing transition frequencies, quantum numbers, lower state energies and transition strengths. This database will provide support for present and future astronomical studies, such as the on-going Orion surveys in preparation for the launch of the Herschel Space Observatory, in identifying isotopic methanol contributions to interstellar spectra.     

Methanol laser lines from torsionally excited co stretch states, and from OH-bend, CH3-rock, and CH3-deformation states

Using a quasi-CW CO₂ oscillator-amplifier combination with peak power 300 Watt, we have generated FIR laser emission in weak absorption bands of CH₃OH. 40 new lines are reported, and their wavelengths are measured with a relative accuracy of 5×10^–5. A total of 72 lines are assigned. 34 of these involve torsional n=1, 2, and 3 states of the CO stretch and the vibrational ground state. The remaining lines are associated with the CH₃-rock, OH-bend, and CH₃-deformation modes. The latter are located 1460 cm^–1 above the ground state, and are pumped by simultaneous vibrational excitation and torsional deexcitation.     

Assignments of optically pumped CD3OH laser lines

Six FIR laser lines from CD₃OH pumped by the 10R(36) and the 10R(18) CO₂ laser lines are assigned to specific rotational energy levels in the excited C–0 stretch state. It is found that their upper laser levels are shifted by a Fermi resonance between the C–0 stretch vibration and the third and forth harmonics of the torsional mode. The Fermi resonance shifts are +0.332 cm^–1 and +2.251 cm^–1 for the upper laser levels pumped by the 10R(36) and the 10R(18) CO₂ laser lines, respectively. Calculated frequencies of the pump and the laser transitions agree with those of the pump CO₂ laser lines and the observed FIR laser lines within estimated accuracy.     

Far infrared spectrum of methylamine

The far-infrared (FIR) spectrum of CH₃NH₂ has been studied in the 25–125 cm^–1 region at a resolution of 0.005 cm^–1 with a BOMEM Fourier transform spectrometer. All of the^rR branches with K rotational quantum number from 5 to 13 have been identified for A-a and E-a torsion-inversion symmetries in the ground torsional state, as well as some branches of A-s and E-s symmetries and some in excited torsional states. The observed branches have been fitted to series expansions in order to determine the branch origins.     

The AB2-XA1 electronic transition of NO2: A rovibronic survey covering 14 300-18 000 cm

More than 250 rotationally resolved vibrational bands of the A²B₂-X²A₁ electronic transition of ¹⁵NO₂ have been observed in the 14 300-18 000 cm⁻¹ range. The bands have been recorded in a recently constructed setup designed for high resolution spectroscopy of jet cooled molecules by combining time gated fluorescence spectroscopy and molecular beam techniques. The majority of the observed bands has been rotationally assigned and can be identified as transitions starting from the vibrational ground state or from vibrationally excited (hot band) states. An exceptionally strong band is located at 14 851 cm⁻¹ and studied in more detail as a typical benchmark transition to monitor ¹⁵NO₂ in atmospheric remote sensing experiments. Standard rotational fit routines provide band origins, rotational and spin rotation constants. A subset of 177 vibronic levels of ²B₂ vibronic symmetry has been analyzed in the energy range between 14 300 and 17 250 cm⁻¹, in terms of integrated density and using Next Neighbor Distribution. It is found that the overall statistical properties and polyad structure of ¹⁵NO₂ are comparable to those of ¹⁴NO₂ but that the internal structures of the polyads are completely different. This is a direct consequence of the X²A₁-A²B₂ vibronic mixing.     

High-resolution far-infrared spectroscopy of C-13 methanol

The high-resolution far-infrared (FIR) Fourier transform spectrum of¹³CH₃OH has been studied from 25–350 cm^–1, andb-type^rR-branches in the torsional ground state have been assigned. The branches have been fitted to phenomeno-logical expansion parameters, which reproduce the branch frequencies generally to well within ±0.001 cm^–1. An interesting and relatively novel K=4 perturbation, localized to levels around J=18, has been observed between (nK)=(019) and (125) states.     

CW-Cavity Ring Down Spectroscopy of O3. Part 3: Analysis of the 6490–6900 cm region and overview comparison with the O3 main isotopologue

This paper is devoted to the third part of the analysis of the very weak absorption spectrum of the ¹⁸O₃ isotopologue of ozone recorded by CW-Cavity Ring Down Spectroscopy between 5930 and 6900 cm⁻¹. In the two first parts [A. Campargue, A. Liu, S. Kassi, D. Romanini, M.-R. De Backer-Barilly, A. Barbe, E. Starikova, S.A. Tashkun, Vl.G. Tyuterev, J. Mol. Spectrosc. (2009), doi: 10.1016/j.jms.2009.02.012 and E. Starikova, M.-R. De Backer-Barilly, A. Barbe, Vl.G. Tyuterev, A. Campargue, A.W.Liu, S. Kassi, J. Mol. Spectrosc. (2009) doi: 10.1016/j.jms.2009.03.013], the effective operators approach was used to model the spectrum in the 6200–6400 and 5930–6080 cm⁻¹ regions, respectively. The analysis of the whole investigated region is completed by the present investigation of the 6490–6900 cm⁻¹ upper range. Three sets of interacting states have been treated separately. The first one falls in the 6490–6700 cm⁻¹ region, where 1555 rovibrational transitions were assigned to three A-type bands: 3ν₂ + 5ν₃, 5ν₁ + ν₂ + ν₃ and 2ν₁ + 3ν₂ + 3ν₃ and one B-type band: ν₁ + 3ν₂ + 4ν₃. The corresponding line positions were reproduced with an rms deviation of 18.4 × 10⁻³ cm⁻¹ by using an effective Hamiltonian (EH) model involving eight vibrational states coupled by resonance interactions. In the highest spectral region – 6700–6900 cm⁻¹ – 389 and 183 transitions have been assigned to the ν₁ + 2ν₂ + 5ν₃ and 4ν₁ + 3ν₂ + ν₃ A-type bands, respectively. These very weak bands correspond to the most excited upper vibrational states observed so far in ozone. The line positions of the ν₁ + 2ν₂ + 5ν₃ band were reproduced with an rms deviation of 7.3 × 10⁻³ cm⁻¹ by using an EH involving the {(054), (026), (125)} interacting states. The coupling of the (431) upper state with the (502) dark state was needed to account for the observed line positions of the 4ν₁ + 3ν₂ + ν₃ band (rms = 5.7 × 10⁻³ cm⁻¹).The dipole transition moment parameters were determined for the different observed bands. The obtained set of parameters and the experimentally determined energy levels were used to generate a complete line list provided as Supplementary Materials.The results of the analyses of the whole 5930–6900 cm⁻¹ spectral region were gathered and used for a comparison of the band centres to their calculated values. The agreement achieved for both ¹⁸O₃ and ¹⁶O₃ (average difference on the order of 1 cm⁻¹) indicates that the used potential energy surface provides accurate predictions up to a vibrational excitation approaching 80% of the dissociation energy. The comparison of the ¹⁸O₃ and ¹⁶O₃ band intensities is also discussed, opening a field of questions concerning the variation of the dipole moments and resonance intensity borrowing by isotopic substitution.     

New combination bands in CCH2 around 0.83 μm recorded using FT-ICLAS

Fourier-transform intracavity laser absorption spectroscopy allowed five ¹²C¹³CH₂ Σ⁺-Σ⁺ bands, all from the ground state, to be identified in the 0.83 μm range. Their rotational analysis was performed and rotational constants are provided. Three of these bands, with origins at 11616.9684(18), 11737.2356(14), and 11761.0322(23) cm⁻¹, have never been reported before. Their upper states are assigned to , respectively.     

High-resolution infrared analysis of the ν7 band of cis-ethylene-d2 (cis-C2H2D2)

The spectrum of the ν₇ band of cis-ethylene-d₂ (cis-C₂H₂D₂) has been recorded with an unapodized resolution of 0.0063 cm⁻¹ in the 740-950 cm⁻¹ region using a Bruker IFS 125 HR Fourier transform infrared spectrometer. By fitting 2186 infrared transitions of ν₇ with a standard deviation of 0.00060 cm⁻¹ using a Watson’s A-reduced Hamiltonian in the I^r representation, accurate rovibrational constants for ν₇ = 1 state have been derived. The band center of ν₇ has been found to be 842.20957 ± 0.00004 cm⁻¹. In a simultaneous fit of 1331 infrared ground state combination differences from the present ν₇ transitions, together with 22 microwave frequencies, ground state constants have been improved. The rms deviation of the ground state fit was 0.00027 cm⁻¹.     

Fourier transform spectroscopy of the CO-stretching band of O-18 methanol

The high-resolution Fourier transform spectrum of the ν₈ CO-stretching band of CH₃¹⁸OH between 900 and 1100 cm⁻¹ has been recorded at the Canadian Light Source (CLS) synchrotron facility in Saskatoon, and the majority of the torsion-rotation structure has been analyzed. For the ν_t = 0 torsional ground state, subbands have been identified for K values from 0 to 11 for A and E torsional symmetries up to J values typically well over 30. For ν_t = 1, A and E subbands have been assigned up to K = 7, and several ν_t = 2 subbands have also been identified. Upper-state term values determined from the assigned transitions using the Ritz program have been fitted to J(J + 1) power-series expansions to obtain substate origins and sets of state-specific parameters giving a compact representation of the substate J-dependence. The ν_t = 0 subband origins have been fitted to effective molecular constants for the excited CO-stretching state and a torsional barrier of 377.49(32) cm⁻¹ is found, representing a 0.89% increase over the ground-state value. The vibrational energy for the CO-stretch state was found to be 1007.49(7) cm⁻¹. A number of subband-wide and J-localized perturbations have been seen in the spectrum, arising both from anharmonic and Coriolis interactions, and several of the interacting states have been identified.     

The ν12 band of ethylene-1-C (CCH4) by high-resolution FTIR spectroscopy

The Fourier transform infrared (FTIR) spectrum of the ν₁₂ fundamental band of ethylene-1-¹³C (or ¹³C¹²CH₄) was recorded with an unapodized resolution of 0.0063 cm⁻¹ in the wavenumber region of 1360-1520 cm⁻¹. Rovibrational constants for the upper state (ν₁₂ = 1) up to five quartic and two sextic centrifugal distortion terms were derived for the first time by assigning and fitting a total of 879 infrared transitions using a Watson’s A-reduced Hamiltonian in the I^r representation. The root-mean-square deviation of the fit was 0.00066 cm⁻¹. The ground state rovibrational constants were also determined by a fit of 523 combination-differences from the present infrared measurements, with a rms deviation of 0.00090 cm⁻¹. The A-type ν₁₂ band which is centred at 1439.34607 ± 0.00004 cm⁻¹ was found to be relatively free from local frequency perturbations. From the ν₁₂ = 1 rovibrational constants obtained, the inertial defect Δ₁₂ was found to be 0.242826 ± 0.000002 μŲ.     

Laser isotope separation of titanium by two-step photoionization

Titanium isotopes were selectively excited and photoionized using a two-step photoionization method, and the isotope separation was demonstrated, in which a separation factor of around 15 for⁵⁰Ti was obtained. Spectroscopic parameters such as isotope shifts, photo-ionization cross section and excited state lifetimes were also measured. Isotope shifts up to 0.92 GHz were obtained for the transitions between 0 and 19938 cm^–1 or between 170 and 20006 cm^–1 among five isotopes. The cross section is 7.4×10^–17 cm² for the photo-ionization. The excited state lifetimes are 330±20 ns for 19938 cm^–1, 260±15 ns for 20006 cm^–1 and 250±15 ns for 20126 cm^–1.     

Reinvestigation of the (4, 20) band of the O2 second negative system

High resolution absorption spectra of the (4, 20) band in the second negative system (A²Π_u–X²Π_g) of O₂⁺ cation were measured and analyzed in the range of 11 900–12 300 cm^–1 via optical heterodyne velocity modulation spectroscopy. Precise molecular constants of the levels involved were obtained by a nonlinear least-squares fitting procedure combining with our previous spectra of the (4, 19) and (6, 20) bands.     

Submillimeter laser action of CW optically pumped CF2Cl2 (Fluorocarbon 12)

Eleven new CW far infrared (FIR) laser lines have been observed in the 600 m–1200 m range from the CF₂Cl₂ (Fluorocarbon 12) molecule optically pumped by a CO₂ laser. A 510^–4–10^–3 accuracy is achieved in the measurement of the FIR wavelengths.The frequency offset between the CO₂ pump center and the absorption line centers are measured using the transferred Lamb dip technique. Owing to a recent spectroscopic study of the CF₂ ³⁵Cl₂ molecule three lines may be assigned with great confidence as rotational transitions in thev ₆ vibrational band 923 cm^–1 of this main isotope.     

The high resolution FTIR spectrum of the ν2 band of formaldehyde isotopomer H2CO

The Fourier transform infrared (FTIR) absorption spectrum of the ν₂ fundamental band of the formaldehyde isotopomer H₂¹³CO was recorded at an unapodized resolution of 0.0063 cm⁻¹ in the 1630–1780 cm⁻¹ region. Upper state (ν₂ = 1) rovibrational constants inclusive of three rotational, five quartic, and six sextic centrifugal distortion constants were accurately determined by assigning and fitting 447 unperturbed infrared transitions with a rms deviation of 0.00056 cm⁻¹ using Watson’s A-reduced Hamiltonian in the I^r representation. Analysis of new transitions measured in this work yielded more higher-order upper state constants with greater accuracy than previously reported. The band center of the A-type ν₂ band was found to be 1707.980943 ± 0.000058 cm⁻¹ while the calculated inertial defect Δ₂ of the H₂¹³CO molecule was 0.09581 ± 0.00004 μŲ.     

The ν12 band of C2D4

The Fourier transform infrared (FTIR) absorption spectrum of the ν₁₂ fundamental band of ethylene-d₄ (C₂D₄) was recorded in the 1017-1137 cm⁻¹ region with an unapodized resolution of 0.0063 cm⁻¹. Upper state (v₁₂ = 1) rovibrational constants consisting of three rotational and five quartic constants were improved by assigning and fitting 2103 infrared transitions using Watson’s A-reduced Hamiltonian in the I^r representation. The band centre of the A-type ν₁₂ band is found to be 1076.98480 ± 0.00002 cm⁻¹. The present analysis covering a wider wavenumber range and higher J and K_c values yielded upper state constants including the band centre which are more accurate than previously reported. The rms deviation of the upper state fit is 0.00045 cm⁻¹. Improved ground state rovibrational constants were also determined from the fit of 1247 ground state combination differences (GSCD) from the presently-assigned infrared transitions of the ν₁₂ band of C₂D₄. The rms deviation of the GSCD fit is 0.00049 cm⁻¹. In the rovibrational analysis, local frequency perturbations were not detected even at high J and K_a values. The calculated inertial defect Δ₁₂ is 0.32551 ± 0.00001 μŲ. The line intensities of the individual transitions in the ν₁₂ band were measured and the band strength of 39.8 ± 2.0 cm⁻² atm⁻¹ was derived for the ν₁₂ band of C₂D₄.     

The Ground State Spectroscopic Parameters and Equilibrium Structure of PD3

Infrared spectra of PD₃ have been measured in the 20-320 cm⁻¹ range and in the region of the ν₂/ν₄ and ν₁/ν₃ fundamental bands near 750 and 1690 cm⁻¹, respectively, with a resolution of ca. 0.0025 cm⁻¹. Furthermore, submillimeter-wave spectra covering the J=4-3, 13-12, and 14-13 clusters in the vibrational ground state were recorded. The observed ΔJ=+1 rotational lines were augmented by about 5500 ground state combination differences formed from transitions belonging to the fundamental bands. Of these, 1300 involved perturbation-allowed lines with ΔK≠0. These data and observations taken from the literature were appropriately weighted and fitted to 14 ground state molecular constants. The A and B reductions of the rotational Hamiltonian were found to be equivalent. Improved effective ground state and equilibrium structures were determined for both PH₃ and PD₃; the equilibrium structures, r_e (PH)=141.1607(83) pm and α_e (HPH)=93.4184(95)° and r_e (PD)=141.1785(57) pm and α_e (DPD)=93.4252(68)°, are in good agreement.     

D2O: ICLAS between 13 600 and 14 020 cm and normal mode labeling of the vibrational states

The high resolution absorption spectrum of dideuterated water, D₂¹⁶O, has been recorded by Intracavity Laser Absorption Spectroscopy (ICLAS) in the 13 600-14 020 cm⁻¹ spectral region which is the highest energy region reported so far for this water isotopologue. Because the HD¹⁶O absorption is stronger by three orders of magnitude in the region under study, it was necessary to use high deuterium enrichment in order to minimize the HD¹⁶O absorption lines overlapping the D₂¹⁶O spectrum. With the high sensitivity achieved (noise equivalent absorption α_min ∼10⁻⁹ cm⁻¹), transitions with line strengths on the order of 5 × 10⁻²⁸ cm molecule⁻¹ could be detected. The spectrum analysis, based on recent variational calculations has provided a set of 177 new rovibrational energy levels belonging to six vibrational states.The most complete set of 53 vibrational energy levels of D₂¹⁶O, including the three newly determined band origins, was constructed from an exhaustive review of the literature data. The fitting of the parameters of the vibrational effective Hamiltonian has allowed to reproduce the whole set of vibrational energies with an rms deviation of 0.055 cm⁻¹. This simple model gave consistent vibrational labels of the D₂¹⁶O states up to 18 000 cm⁻¹. Above 15 000 cm⁻¹, Fermi and Darling-Dennison resonance interaction were found to induce strong vibrational mixings of the wave functions in the normal mode basis, leading to ambiguous vibrational labeling.