Pulse flip angles are calculated for three wave mixing, three state cycles of
chiral molecules to produce optimized free induction decay amplitudes
proportional to the enantiomeric excess of a sample, and to produced optimized
degree of state specific enantiomeric separation. These calculations account
for the spatial degeneracy of the levels involved and the resulting
inhomogeneous distribution of transition dipole moments.
It is found that cycles of transitions that include R followed by Q followed
by P branch transitions display only modest reductions of the calculated
optimal signals if spatial degeneracy is ignored. Transitions cycles P - Q - R
are only slightly worse, while the Q - Q - Q cycles are much worse,
increasingly so as the rotational total quantum number increases.Comment: 12 pages , 6 table