Fourier transform far infrared spectrum of CD3OD: detailed analysis in the torsional ground state

High resolution Fourier transform (FT) far infrared (FIR) spectra of CD3OD isotopomer of methanol have been measured in the range 20–350 cm21 at a resolution of 0.0017 cm21 using a Bruker spectrometer. The spectra were recorded in various runs at pressure in the range of 0.2–0.8 mbar both at room temperature and at 260 8C. The spectra show complicated splitting due to strong torsional–rotational interactions in the molecule. Detailed assignments have been achieved mainly for the torsional ground state levels. The assigned transition wavenumbers along with the previously known microwave (MW) [J. Chem. Phys. 23 (1955) 1195; J. Chem. Phys. 56 (1972) 5887; Spectrochim. Acta A 54 (1998) 1375], and recently measured millimeter-wave (MMW) lines [I. Mukhopadhyay, R.A.H. Butler, F.C. DeLucia, E. Herbst, in preparation], were fit to an eighth order Hamiltonian [J. Chem. Phys. 104 (1996) 3914; J. Chem. Phys. 110 (1999) 927; J. Mol. Spectrosc. 193 (1999) 418; Chem. Phys. 263 (2001) 263; Chem. Phys. 257 (2000) 91; Chem. Phys. 280 (2002) 119; Chem. Phys. (2003) in press] with 62 varied parameters. The data set consisted of a total of 3211 transitions with 2959 FIR transitions from the ground torsional state with rotational angular momentum K ranging from 0 to 19 and J ranging from 0 to 45, and 237 MW and MMW transitions. The fit converged with a standard deviation of 0.0007 cm21 for the FIR component of the data and the standard deviation for the MW and MMW transitions was 560 kHz. The standard deviation for the FIR lines is well compared with the estimated experimental accuracy of 0.0002 cm21 for clean unblended lines. Here we report the actual measured wavenumbers with their assignments, some of these were not included in the fit. The complete data set fitted is not included here for the sake of economy of space but can be obtained from IM. q 2004 Elsevier B.V. All rights reserved.