High-order optical nonlinearity in molecular systems is of considerable int
erest, due to the dynamical information it affords, the flexibility in geom
etry it offers, and due to its involvement in the generation of even harmon
ics in isotropic media. Here, attention is focused on several processes who
se optical response is dominated by two electronic states and which involve
the coupling of up to six different optical modes. It is shown that transf
ormation of the electric-dipole interaction provides a convenient means for
ascertaining the role of intramolecular charge transfer on the high-order
nonlinear optics of such systems. The transformation offers calculational e
xpediency and a direct route to expressions for nonlinear molecular polariz
abilities. In particular, the method identifies directly terms dependent on
various powers of the displacement vector for intramolecular charge transf
er.