No abstract

Effects of the size and attachment position of benzyl aryl ether dendrons covalently attached to bis(thiopyrylium) penta- and heptamethines on the optical properties of these dyes in solution and in solid films have been investigated. In dilute solution the low-energy absorption bands of some of the dendronized species differ from those of the parent compounds in having much smaller transition dipole moments, this effect possibly due to differences in ion pairing, while at higher concentrations, dye–dye interactions lead to a decrease in the transition dipole moments of the nondendronized species, but not of the dendronized ones. Consequently, in the high concentration range, dendronized and nondendronized species exhibit similar values of the real part of the microscopic third-order polarizability at 1550 nm. Solid-state film absorption spectra suggest that the dendrons significantly disrupt the chromophore–chromophore interactions seen for the nondendronized species, reducing, but not eliminating, linear absorption losses in the near-IR, and suppressing absorption peaks that are hypsochromically shifted from the solution spectra maximum: centrally placed dendrons have a larger effect than terminal dendronization, so that the corresponding thin-film spectra more closely resemble those seen in solution with increasing generations of dendronization. Z-scan measurements at 1550 nm indicate that the third-order susceptibility of dendronized heptamethine guest–host films depend approximately linearly on doping ratio of dyes and are in reasonable agreement with values extrapolated from solution-derived third-order polarizabilities; in contrast, the susceptibilities of films highly doped with an undendronized analogue fall short of values expected from solution polarizabilities.

The first peripheral postfunctionalization of a hyperbranched polyimide by nonlinear optic chromophores (DR1 derivative) was achieved using two different routes. The first one consists in the esterification of the terminal carboxylic acid groups, whereas the second is based on copper-catalyzed Huisgen reaction of the terminal propargylic ester groups. The resulting polymers display good solubility in classical organic solvents and good filmability because thick films can be prepared (up to 2.7 mum). The second-order nonlinear optical properties were measured by SHG at 1064 nm and we show that these hyperbranched polymers exhibit good poling efficiency and good thermal stability since the electro-optic activity remains stable up to 130 degrees C. These results illustrate the potential of hyperbranched polymers to host second-order nonlinear optical chromophores to replace dendrimers or classical linear polymers generally used in this area.