A non-Markovian theory for the dipolar absorption coefficient of polar diatomic molecules diluted in a non-polar liquid medium is applied to obtain the far-infrared spectra of HCl in liquid Ar at densities between 480 and 100 amagat and T= 162.5 K. The time correlation functions involved in the theo
Theoretical infrared spectra of HCl in liquid SF6: A temperature dependence study
✍ Scribed by J.R. Pérez; D. Luis; S. Velasco; A. Calvo Hernández
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 395 KB
- Volume
- 164
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The fundamental infrared spectra (2700-3100 cm-') of dilure solutions of HCI in liquid SF, at temperatures between 2 18 and 316 K have been calculated by applying a spectral theory based on the decomposition of the rotational motion of the diatomic molecule into two limiting cases: quasi-free rotation and rotational diffusion. From comparison between theoretical and experimental spectra it is possible to deduce quantitative values for a reduced set of statistical parameters involved in the theory and to analyze their behaviour as a function of the solvent temperature. The connection between the rotational structure appearing in these spectra and the parameters is discussed.
📜 SIMILAR VOLUMES
The far-infrared of DCI, HCl and HF in liquid SF, (T= 273 K) are studied by applying a previously reported non-Markovian line-by-line spectral theory in which memory and mixing effects arc explicitly considered. We analyze the importance of both effects in terms of the rotational constant of the dia