Abstract
The difference in interaction energies between two
laevo
molecules, and one
dextro
and one
laevo
, are analysed. Formulae are given for the discriminating terms in the dispersion and induction energies for molecules in fixed orientations, between freely rotating molecules, and molecules rotating about the intermolecular axis. Discrimination in the resonance interaction between optical isomers appears in the retarded interaction (in dipole approximation) as a term with an inverse square dependence on distance in the near zone. Its significance is discussed for pairwise interactions and in crystalline systems.
Cited by
90 articles.
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