Abstract
Neutron "optical activity" or the rotation of the neutron polarization is investigated in the scattering of polarized neutron beams from chiral molecules. A rotation exists to first order in the neutron-electron spin-orbit interaction for randomly oriented target molecules if a total angular momentum (jt+st) and an orbital angular momentum hjt* are transferred coherently to a molecular rotator. The first is the angular momentum developed by incident and scattered waves and spinors through a region of interaction with the magnetic fields generated by electrons bound in the "twisted" potentials characteristic of a chiral molecule. The second is the angular momentum developed by incident and scattered waves through a region of interaction with a network of atomic nuclei having the same twist. The magnetic amplitude must be calculated in the first Born distorted-wave approximation. Distortion causes the magnitudes of the magnetic amplitudes to be distinct for Δl=±1, Δm=±1, and Δl=±1, Δm=0 partial-wave transitions induced by the magnetic forces, thus preventing their cancellation on rotationally averaging the cross section. This distortion is produced by the nuclear background; thus the rotation is of order mNme (neutron-to-electron mass ratio) larger than previous estimates based on the use of the second Born plane-wave magnetic amplitude for forward scattering. However, the present rotation exists only at nonzero scattering angles. This is the first example of a rotation of the neutron polarization which is nonvanishing to first order in a spin-orbit interaction. Its strength makes it an important effect in the use of neutrons to probe molecular structure. We check our result by finding the limit of scattering from spin-independent forces. Here the rotation vanishes, and the incoherent limit for the transfer jt=jt* obtains. This limit is well known from the Fano-Dill or Temkin-Sullivan theory of orbital-angular-momentum transfer to a rotator.