Abstract

A number of new photosensitive copolyacrylates of different composition were obtained by the copolymerization of chiral photochromic benzilidene-p-menthane- 3-one acrylic monomers with a smectogenic monomer containing a hexyloxyphenylbenzoate mesogenic group. The chiral, photochromic monomers differ by the length of the aliphatic spacer and the aromatic fragment. It was found that the introduction of a small number of chiral units into the copolymers (5 mol%) leads to the “degeneration” of the smectic C phase, which characterizes the hexyloxyphenylbenzoate homopolymer, and to the formation of the smectic A phase. An unusual effect of chiral nematic phase induction was observed for copolymers containing chiral side groups with two ring aromatic fragments. It should be pointed out that the chiral nematic phase does not occur in the case of the homopolymers of both initial comonomers. An explanation of this effect, based on the consideration of the chemical structure of the chiral and hexyloxyphenylbenzoate units, was suggested. The optical properties of cholesteric copolymers were investigated; the helical twisting power of the chiral groups of different structures was calculated. The possibility of using such copolymers as new photosensitive materials was demonstrated.

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