Measurements of (18)O-Enriched Ozone Isotopomer Abundances Using High-Resolution Fourier Transform Far-IR Spectroscopy.

The distribution of ozone isotopomers in ozone mixtures produced by electric discharge in mixtures of (16)O(2) and (18)O(2) at 77 K was measured by high-resolution FTIR spectroscopy. It was of key importance to assess not only the total amount of isotopomers of a certain mass but also the relative amounts of corresponding asymmetric and symmetric ozone species of the same mass given as the ratios [(16)O(16)O(18)O]/[(16)O(18)O(16)O] and [(16)O(18)O(18)O]/[(18)O(16)O(18)O]. For many purposes both ratios have been assumed to have the statistical value 2.00. Pure rotational spectra in the far-IR region (30-100 cm(-1)) were recorded for three different (18)O-enriched ozone mixtures, all at 0.00185 cm(-1) resolution. All the spectra were corrected for thermal emission. Linestrengths for individual lines in a particular spectrum were measured by means of a fitting technique taking into account contributions from all other lines in the spectrum. For this purpose theoretical linestrengths for all six ozone species containing (16)O and (18)O obtained from a quantum-number-dependent dipole operator were used. The ratios between observed and theoretical linestrengths were used to determine the abundances of individual isotopomers in a particular ozone mixture. For one of the ozone samples the abundances of all six ozone species were determined within 1% relative uncertainty. For the three ozone mixtures studied, the ratio between asymmetric and symmetric species of mono-(18)O ozone were determined to 1.99(2), 2.01(2), and 2.10(6). The ratio between asymmetric and symmetric species of di-(18)O ozone were determined to 2.51(4), 2.42(10), and 2.46(3). Copyright 2000 Academic Press.

The High-Resolution Infrared Spectrum of 1,2,4-Triazine Vapor between 550 and 1700 cm(-1).

The Fourier transform gas-phase IR spectrum of 1,2,4-triazine between 550 and 1700 cm(-1) was measured with a resolution of ca. 0.003 cm(-1). Comparing with the liquid-phase IR and Raman spectra and using ab initio predictions, most of the fundamental bands of 1,2,4-triazine below 1600 cm(-1) were assigned. From the high-resolution gas-phase spectra, 12 of the fundamental bands were analyzed by the Watson Hamiltonian model to yield upper state spectroscopic constants. A number of local resonances were identified and explained. From a simultaneous ground state combination difference analysis of four of the bands, a set of ground state rotational and centrifugal distortion constants were obtained. Copyright 1999 Academic Press.