A study of photooptical processes in photosensitive cholesteric azobenzene-containing polymer mixture under an action of the polarized and nonpolarized light

New liquid crystalline cholesteric mixture consisting of azobenzene-containing side-chain copolymer and the chiral low-molar-mass dopant (5%) was prepared and its properties were studied. It was shown that freshly prepared spin-coated thin films are optically isotropic. However, the films possess a noticeable circular dichroism with a maxima corresponding to the absorbance of the nonchiral azobenzene fragments. This phenomenon is an evidence for the existence of the helical supramolecular structure elements in the mixture films. An annealing of the films at temperatures above the glass transition leads to the strong increase in the circular dichroism due to formation of the perfect cholesteric phase. UV light irradiation results in the E-Z isomerization of azobenzene groups and the significant drop in circular dichroism values (almost to zero) both for the fresh and the annealed films that is associated with the transition from cholesteric to the fully isotropic state. An action of polarized UV and visible light leads to the photoorientation of azobenzene groups perpendicular to the electric vector of the polarized light. Kinetic features of the photoorientation processes in cholesteric phase in comparison with nematic systems were studied. It has been experimentally found that the helical order to some extent prevents the photoorientation of the side groups. Upon UV irradiation of the thick, planarly-oriented films of the mixture at temperatures higher than glass transition, the selective light reflection maximum is shifted to the long-wavelength spectral region. All photoinduced phenomena occurring in the mixture are thermally reversible and annealing of the films at temperatures above glass transition results in the back recovery to the cholesteric nonoriented state and to the initial helix pitch value.