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Open AccessJournal ArticleDOI

The Refractive Index Dispersion and Polarization of Gases

H. E. Watson, +1 more
- 01 Aug 1936 - 
- Vol. 156, Iss: 887, pp 144-157
TLDR
In this paper, the dispersion of a sample of commoner gases has been determined with some accuracy by measuring the refraction for different wave-lengths, and the dielectric coefficient at different temperatures.
Abstract
In recent years, values of the refractive index of liquids, and sometimes of gases, have been extensively used for determining dipole-moments. Measurements of dielectric coefficients give the sum of the orientation, electronic and atomic polarizations P + Pe +Pa, while the electronic polarization Pe can be calculated approximately from the refractive index. If the dispersion is known, Pe should be given with some accuracy by calculating the refractive index at zero frequency. In order to obtain P, it is necessary to know Pa, a quantity which has only been determined for a few substances, the infra-red spectrum of which has been examined in detail. It is, however, often assumed that Pa is negligible or, at least, small in comparison with Pe. In some cases, an approximation on an empirical basis has been made by assuming that Pa is proportional to Pe, or that Pa + Pe is equal to the value of Pe when calculated from the refractive index for the yellow sodium line. Such assumptions can hardly be regarded as satisfactory. In liquids, determination of the polarization is complicated by the necessity of employing a solvent, but, with gases, no such difficulty exists. Pa can therefore be determined with some accuracy by measuring the refraction for different wave-lengths, and the dielectric coefficient at different temperatures. Numerous measurements of the refractive index of the commoner gases have been made, but the results of different observers are not always in agreement and frequently the dispersion has not been determined. The dielectric coefficient of the same sample of gas seems never to have been measured.

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Book ChapterDOI

Molecular Refractivity and Polarizability

TL;DR: In this article, molecular refractivity and polarizability of a particle is defined as the dipole moment induced by an electric field of unit intensity, and the principal polarizabilities of molecules can be analyzed in terms of anisotropic bond polarisation.
Journal ArticleDOI

Dispersion energy constants C 6(A, B), dipole oscillator strength sums and refractivities for Li, N, O, H2, N2, O2, NH3, H2O, NO and N2O

TL;DR: In this paper, the orientation-averaged long-range dipole-dipole dispersion energy coefficients, C 6(A, B), have been determined for all possible pair interactions involving ground state H, Li, N, O, H2, N2, O2, NH3, H 2O, NO, and N2O.
Journal ArticleDOI

An efficient approach for calculating vibrational wave functions and zero-point vibrational corrections to molecular properties of polyatomic molecules

TL;DR: In this article, the contribution to the zero-point vibrational correction from the anharmonicity of the potential is included in the calculations by performing a perturbation expansion of the vibrational wave function around an effective geometry.
Journal ArticleDOI

Electronic and relaxation contribution to linear molecular polarizability. An analysis of the experimental values

TL;DR: In this paper, the mean values of the electronic polarizability tensors αe and αr were derived for more than 650 molecules, where αe is the mean value of the dielectric constant and α r is the static polarization of the molecule.
Journal ArticleDOI

Total dissociation cross section of CF/sub 4/ and other fluoroalkanes for electron impact

TL;DR: In this article, it was shown that the Bethe asymptotic behavior is not yet attained in the energy range of more than a threshold (approx125 eV) and 600 eV.
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