Published January 2018 | Version v1
Journal article

Line intensity measurements and analysis in the ν3 band of ruthenium tetroxide

  • 1. Service de Chimie Quantique et Photophysique C.P. 160/09, Université Libre de Bruxelles, 50 avenue F. D. Roosevelt, B-1050 Brussels (Belgium)
  • 2. Den-Service d'Etude du Comportement des Radionucléides (SECR), CEA, Université Paris-Saclay, F-91191 Gif-sur -Yvette (France)
  • 3. Laboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université Bourgogne Franche-Comté, 9 avenue Alain Savary, BP 47870, F-21078 Dijon Cedex (France)
  • 4. MONARIS, UMR 8233, Université Pierre et Marie Curie, 4 Place Jussieu, case 49, F-75252 Paris Cedex 05 (France)
  • 5. Synchrotron SOLEIL, AILES Beamline, L'Orme des Merisiers, BP48, F-91192 St-Aubin Cedex (France)

Description

Highlights: • High resolution Fourier transform spectroscopy of pure 102RuO4 from 895 to 945 cm–1. • Six experiments conducted at the AILES beamline of SOLEIL using synchrotron radiation. • 266 line intensities measured for the first time in the ν3 band. • 198 line intensities fitted using a global tensorial model (RMS deviation of 8.0%). • HITRAN-formatted list of 3373 lines for the ν3 band of 102Ru16O4. - Abstract: 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 10 μm, associated with the excitation of the infrared active stretching mode ν3. 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 Reymond–Laruinaz et al, J Mol Spectrosc 2015;315:46–54], the measured line intensities were assigned and dipole moment parameters determined. A HITRAN-formatted frequency and intensity line list was generated.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jqsrt.2017.09.016

Additional details

Identifiers

DOI
10.1016/j.jqsrt.2017.09.016;
PII
S0022-4073(17)30629-5;

Publishing Information

Journal Title
Journal of Quantitative Spectroscopy and Radiative Transfer
Journal Volume
204
Journal Page Range
p. 103-111
ISSN
0022-4073
CODEN
JQSRAE

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.