It is shown that the numerical value of the optical activity of an optically active compound is markedly reduced if the groups surrounding the asymmetric atoms in the compound possess a threefold axial symmetry about the bonds connecting them with the asymmetric atoms. This threefold symmetry may be either inherent in the groups themselves, or it may be acquired by them through the free rotation of the groups about these bonds or by their orienting themselves to equal extents in each of the three possible equilibrium positions about each bond. The order of magnitude of the numerical value of the optical activity is thus a measure of the freedom of orientation about single bonds of the groups in an asymmetric molecule. That this effect is actually a dominant factor in determining the order of magnitude of the optical activity is proved by the contrast in the optical activities of cyclic and open chain compounds. It is shown to have an important effect on the temperature coefficient of optical activity and to lie at the root of the observed differences in the orders of magnitude of the rotatory powers of liquids and crystalline solids. The structures of certain sulphur compounds, polypeptides, and proteins are discussed in the light of the magnitudes of their optical activities.
展开▼
