Collision-induced rotational Raman scattering by tetrahedral and octahedral molecules

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Abstract
The long tails at high Stokes and anti-Stokes frequencies observed in Rayleigh scattering from compressed methane, carbon tetrafluoride and sulphur hexafluoride are attributed to induced rotational transitions. The longest-range contribution to the collision-induced polarizability, the dipoleinduced-dipole term in R -3, where R is the separation of a pair of molecules, does not fluctuate with molecular rotation. However, the dipole-quadrupole polarizability A of the tetrahedron leads to a rotating contribution in R -4. The dipole-octopole polarizability E of an octahedron and a tetrahedron leads to a contribution in R -5 which also rotates with the molecule. The rotational transitions associated with these polarizabilities can explain both the intensity and the shape of the long tails. Approximate values of A for CH4 and CF4 and of E for SF6 are deduced. As in the monatomic case, there is a simple relationship between the total scattered intensity and the second Kerr virial coefficient.