Dependence of the Two-Photon Absorption Cross Section on the Conjugation of the Phenylacetylene Linker in Dipolar Donor−Bridge−Acceptor Chromophores Dependence of the Two-Photon Absorption Cross Section on the Conjugation of the Phenylacetylene Linker in

The nonlinear optical properties of four isomeric dipolar two-photon chromophores are compared. The chromophores consist of a carbazole electron donor coupled to a naphthalimide electron acceptor by a phenylacetylene bridge. By variation of the connectivity of the bridge at the phenyl groups, four compounds with 0, 1, and 2 meta linkages are synthesized. The linear and nonlinear optical properties of these compounds are measured. Despite similar linear absorption cross sections, the two-photon absorption cross section δ of the all-meta compound is almost a factor of 10 lower than the all-para compound. By taking the detailed molecular conformations into account in order to calculate accurate dipole moment changes, we find that the decrease in δ results largely from the decreased charge transfer ability with increasing number of meta linkages. We find that a two-state model can be used to predict semiquantitatively the observed trend in δ on the basis of the linear optical properties of the molecules. This work illustrates the dramatic effect the ground-state polarizability can have on the nonlinear optical response of organic compounds and also provides a way to quantify the ability of meta linkages to inhibit charge transfer in their ground-state configuration