Synthesis, photo-reaction and photo-induced liquid crystal alignment of soluble polyimide with pendant cinnamate group

In this paper, the synthesis, photo-reaction and photo-induced liquid crystal alignment of a polyimide with a pendant cinnamate group are reported. The polyimide was synthesized by the thermal imidization of the polyamic acid derived from 4,4-(hexafluoro-isopropylidene)-diphthalic anhydride and hydroxydiaminopropane, followed by the attachment of the cinnamate group to the main chain polyimide. The surface of thin layers of the polyimide was found to be preferentially occupied by the pendant cinnamate groups, and liquid crystal alignment on the polyimide thin film exposed to polarized UV was independent of the cinnamate content. The thermal stability of the photo-induced liquid crystal alignment was enhanced with decrease in the cinnamate content. This could be attributed to the strong interchain interaction of the polyimide chains which prevents thermal randomization of the photo-product of the pendant cinnamates. The dependences of the photo-reaction temperature and the annealing temperature of the alignment layer on the azimuthal anchoring energy of the photo-aligned liquid crystal suggest that the local stress developed during the UV irradiation profoundly influences the thermal stability of the liquid crystal alignment.