Valery P. Shibaev

New cholesteric polymeric mixture containing nematic side‐chain homopolymer, 2 wt% of photochromic diarylethene dopant and 5 wt% of chiral‐photochromic dopant based on cinnamic acid and isosorbide was prepared. Upon UV irradiation of planarly‐oriented mixture films at room temperature, a transformation of open colorless form of diarylethene dopant into a closed colored form takes place, which is followed by the appearance of an intense absorption maximum in the visible spectral region and decreasing selective light reflection intensity. This process is photo‐ and thermo‐reversible and many cycles ‘recording‐erasing’ can be realized. UV irradiation and subsequent annealing of the films lead to untwisting of the cholesteric helix and cause an irreversible shift of selective light reflection to the long‐wavelength region. This process is explained by the E‐Z isomerization of chiral photochromic groups of the dopant relative to a CC bond accompanied by a decrease in their twisting ability.It has been shown, that the use of the material prepared in this work provides an opportunity to record two images at the same time: one image is due to a change in the helical pitch and another (second) image is due to the photochromism of diarylethene dopant. It is pertinent to note that using the approach developed in this work allows one to widely vary the range of materials exhibiting dual photochromism. It was demonstrated that the mixture under study shows advantage as new photosensitive material for optics, optoelectronics and data recording. Copyright © 2002 John Wiley & Sons, Ltd.

The phase behaviour and optical properties of the mixture based on cholesteric copolymer with 6 wt% of a photochromic dithienylethene dopant was studied. It was shown that planarly-oriented films of the mixture possess a selective light reflection in the visible region of the spectrum (λ_max ∼600 nm). UV irradiation of the mixture film leads to the appearance of an intense absorbance peak in the spectral range coinciding with the selective reflection band. This process is associated with the photocyclization of dopant and the “degeneration” of the selective light reflection. The photoinduced coloured form of dopant is thermally stable, but subsequent irradiation of the film by visible light (633 nm) induces a back decoloration process. For the first time the influence of temperature on the rates of forward and back photoprocesses in such polymeric liquid crystalline films was studied. The potential for the use of such a type of material for reversible data recording and storage was demonstrated.

A new photosensitive chiral dopant based on cinnamic acid and isosorbide was synthesised. UV light action leads to E-Z photoisomerization of the dopant about C=C double bond of cinnamoyl fragment. Mixtures of the dopant with nematic and cholestric polymers were studied. It was shown, that planarly-oriented films of mixtures possess a selective light reflection in ultraviolet, visible and infrared regions of spectrum depending on the dopant concentration. The helical twisting power of the chiral dopant was calculated. UV light action on mixture films leads to a shift of selective light reflection peak to the long wavelength region of spectrum, which is explained by photoisomerization and decrease of the helical twisting power of the dopant. Kinetics of the process of photoinduced untwisting of the cholesteric helix was studied. Advantages of the use of the synthesised dopant and of mixtures based on it were demonstrated in comparison to earlier studied chiral-photochromic materials for optical data recording and storage.