Discrepancies between the theoretical and experimental values of: (a) the frequency splitting of the Pake doublet, (b) the values of the quadrupole coupling constant, and (c) the orientational transition temperature for solid H2 are pointed out. It is shown that these discrepancies are significant and can be at least partially explained by consideration of the interactions between molecular rotations and lattice vibrations. A table of revised experimental values of the quadrupole coupling constant, T, is given.
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A. B. Harris (2009) studied this question.
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