Measurements and Calculations of the Halfwidth of Two Rotational Transitions of Water Vapor Perturbed by N2, O2, and Air.

In this paper we report the results of both an experimental and theoretical study of the halfwidths of two transitions of water vapor. Measurements on the lines of the H216O and H218O isotopomers located at 325.1 and 203.4 GHz, respectively, were carried out in the temperature range 300-393 K, with N2 and O2 as perturbing gases. The foreign-broadening coefficients and their temperature-dependence parameters were determined assuming a Voigt profile and the usual temperature dependence for the halfwidth. The retrieved values are compared to values calculated using the complex semiclassical formalism of Robert and Bonamy. The assumed intermolecular potential is a combination of electrostatic and atom-atom components. This last contribution is defined as the sum of pairwise Lennard-Jones 6-12 interactions between the atoms of H2O and the atoms of the perturbing molecules expanded to eighth order. Also calculated are the pressure-induced shifts of the spectral lines for temperatures from 200 to 400 K. Calculated and experimental results are in good agreement, within +/-3.2%, except for the N2-broadening temperature coefficients, for which there are discrepancies as high as 23%. Air-broadening parameters are determined following the classical relation: gamma (air) = 0.79gamma (N2) + 0.21gamma (O2). Copyright 1999 Academic Press.

Relaxation and Lineshape of the 500.4-GHz Line of Ozone Perturbed by N(2) and O(2).

N(2)- and O(2)-broadened linewidths of the J = 34(2,32) <-- 34(1,33) transition of ozone located at 500.4 GHz have been measured at three temperatures in the 247-295 K range by using a video-type spectrometer. Besides the Voigt profile commonly used as theoretical model for millimeter-wave investigations, different other theoretical lineshapes, the speed-dependent Voigt profile, the Galatry profile, and the speed-dependent Galatry profile, have been considered to analyze the experimental spectra, to retrieve the pressure-broadening parameters, and to give an account of the pointed out line-narrowing effect. The results for O(3) perturbed by N(2) and O(2) are finally compared to calculations based on the complex semiclassical theory of Robert and Bonamy, and with previous reported values involving the same kind of transitions. Finally, it is shown that observed line narrowings result nearly exclusively from the dependence of relaxation on molecular speeds. Copyright 2000 Academic Press.

Rotational Spectra of the Isotopic Species of Chloroform: Experimental and Ab Initio Structures.

The millimeter-wave spectra of three different samples of chloroform (CHCl3, CDCl3, and 13CHCl3) have been measured between 145 and 470 GHz which corresponds to J values between 22 and 70. We report accurate rotational and centrifugal distortion constants for the ground vibrational states of 11 isotopic species. The experimental ro, rs, rIepsilon, rrhom, and rz structures have been determined using the determined rotational constants. The structure has also been calculated ab initio at the SCF, MP2, RQCISD, and B3LYP levels using triple zeta polarized basis sets. The experimental results are found in excellent agreement with the ab initio predictions. An approximate equilibrium structure has been obtained by combining the experimental results and the ab initio calculations: re(C-H) = 1.080 (2) Å, re(C-Cl) = 1.760 (2) Å, and anglee(HCCl) = 108.23 (2) degrees. Copyright 1998 Academic Press.

Analysis of the Rotational Spectra of SiH3CN and Its Isotopomers: Experimental and Ab Initio Determinations of the Dipole Moment and the Structure.

The ground state rotational spectra of SiH3CN and its 29Si, 30Si, 13C, 15N, d1, d2, and d3 isotopic species have been measured by Fourier transform microwave spectroscopy and by millimeterwave spectroscopy. Accurate rotational, centrifugal distortion, and 14N and D nuclear quadrupole coupling constants have been derived. The dipole moment of the parent species has also been measured, µ = 3.4400(42) D. The structure, force field, dipole moment, and nuclear quadrupole coupling constants have been calculated ab initio at the SCF, MP2, and B3LYP levels using triple zeta polarized basis sets. The experimental ro, rs, and rz structures have been determined. An approximate equilibrium structure has been obtained by combining the experimental results and the ab initio calculations: re(C&tbond;N) = 1.159 Å, re(Si&sbond;C) = 1.848 Å, re(Si&sbond;H) = 1.470 Å, and angle(HSiC) = 107.4 degrees. Copyright 1998 Academic Press.