|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|5426990||1397241||2018||9 صفحه PDF||ندارد||دانلود رایگان|
â¢High resolution Fourier transform spectroscopy of pure 102RuO4 from 895 to 945Â cmâ1.â¢Six experiments conducted at the AILES beamline of SOLEIL using synchrotron radiation.â¢266 line intensities measured for the first time in the Î½3 band.â¢198 line intensities fitted using a global tensorial model (RMS deviation of 8.0%).â¢HITRAN-formatted list of 3373 lines for the Î½3 band of 102Ru16O4.
Ruthenium tetroxide (RuO4) is a heavy tetrahedral molecule characterized by an unusual volatility near ambient temperature. Because of its chemical toxicity and the radiological impact of its 103Ru and 106Ru isotopologues, the possible remote sensing of this compound in the atmosphere has renewed interest in its spectroscopic properties. The present contribution is the first investigation dealing with high-resolution line-by-line intensity measurements for the strong fundamental band observed near 10Â Î¼m, associated with the excitation of the infrared active stretching mode Î½3. It relies on new, high resolution FTIR spectra recorded at room temperature, using a specially constructed cell and an isotopically pure sample of 102Ru16O4. Relying on an effective Hamiltonian and associated effective dipole moment [S ReymondâLaruinaz etÂ al, J Mol Spectrosc 2015;315:46â54], the measured line intensities were assigned and dipole moment parameters determined. A HITRAN-formatted frequency and intensity line list was generated.
Journal: Journal of Quantitative Spectroscopy and Radiative Transfer - Volume 204, January 2018, Pages 103-111