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Composite systems of liquid crystals (LCs) and polymers have been extensively studied in various forms such as polymer-dispersed LCs and polymer-stabilised LCs. Blending LCs and polymers is an effective approach to design functional materials with stimuli responsiveness and durability. Here, we show the development of a novel composite material with crosslinked azobenzene LC polymer (PAzo) and poly (dimethylsiloxane) (PDMS) aiming at the improvement of photomobile polymer materials in mechanical properties. The composite films were prepared by photopolymerisation of azobenzene monomers in PDMS elastomers. By forming phase separated structure, in which PAzo chains were dispersed in PDMS matrix, fracture strain of photomobile polymer materials was significantly enhanced. The composite film showed macroscopic bending upon irradiation with UV light. This result implies that PAzo domains in polymer matrix can work as microactuators to afford macroscopic deformation of the whole film. The further improvement of this system in photomechanical properties would be feasible through adequate control of composition and the alignment of mesogens. [ABSTRACT FROM AUTHOR]

The article discusses the mechanical properties of flexible films, such as surface strain of largely bending films, which are considered as key to design of stretchable electronic devices, wearable biointegrated devices, and soft microactuators or robots. It notes that the existing methods are mainly based on strain-gauge measurements that ask miniaturized array sensors, lead wires, and complicated calibrations.

(t‐BuNSiMe2Flu)TiMe2 (1) activated with Me3Al‐free methylaluminoxane (dried MAO) which conducts vinyl addition polymerization of norbornene (N) with very high activity was applied for homopolymerization of N derivatives (i.e., 5‐vinyl‐2‐norbornene (5V2N), 5‐ethylidene‐2‐norbornene (5E2N), dicyclopentadiene (DCPD)) at 40 °C. The activities for the N derivatives were about two orders of magnitude lower than that for N and decreased in the following order: 5E2N ≫ 5V2N ≫ DCPD. Copolymerization of ethene (E) and 5E2N under an atmospheric pressure of E was then conducted by 1‐dried MAO. The copolymerization proceeded with better activity than the homopolymerization of 5E2N and gave poly(E‐co‐5E2N) with narrow molecular weight distribution. The content of the ethylidene group in poly(E‐co‐5E2N) was controlled by the feed ratio of 5E2N/E. The Tg value of the copolymer changed from 70 °C to 155 °C according to the 5E2N content from 27 mol % to 68 mol %. The addition of N as a third monomer to the E‐5E2N copolymerization improved the activity and raised the Tg values of the terpolymer above 200 °C. The content of 5E2N was controlled by the 5E2N/N ratio with keeping the high Tg values. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4581–4587, 2007 [ABSTRACT FROM AUTHOR]

After being pre-treated upon irradiation of unpolarized light at 366 nm, an azobenzene-containing liquid-crystalline polymer film was photoinduced alignment by one linearly polarized laser beam at 488 nm, leading to a large birefringence of 0.21. Then holographic gratings were recorded in the pre-irradiated polymer films by interference of two coherent laser beams. Little surface relief was obtained by the holographic recording process, indicating that a refractive-index grating paid most of contributions to the diffraction efficiency. Because the cooperative motion of the azobenzene mesogens were eliminated in the cis-azobenzene-rich isotropic film by the pre-irradiation, multi-processes of the refractive-index gratings were successfully achieved. The obtained grating structures were clearly shown in the polarizing optical microscopic pictures, which were also verified by their diffraction patterns. The azobenzene-containing liquid-crystalline polymer used in this study has potential application in high-density information storage. [ABSTRACT FROM AUTHOR]

Three azobenzene acrylate monomers containing alkyl spacers of different length were synthesized. Thermodynamic and mesomorphic properties of the monomers were measured by differential scanning calorimetry and polarizing optical microscopy. A crosslinker with the undecyl spacer was also synthesized to prepare crosslinked liquid-crystalline polymer films by photopolymerization. Polarized UV spectra and polarizing optical micrographs demonstrated that the mesogens are aligned homogeneously in the films. Low glass transition temperature of the films enabled them to bend near room temperature upon UV irradiation. Besides, the films generally bent away from the light source before they at last bent towards the light irradiation. [ABSTRACT FROM AUTHOR]

The azobenzene liquid-crystalline gel (LCG) films with macroscopic uniaxial alignment were prepared to investigate photoresponsive behavior. By polarizing microscopy, fiber-like structures aligned in one direction were observed. Furthermore, with a confocal laser scanning microscope (CLSM), it was confirmed that the fiber-like structures were formed even in the bulk of the LCGs. When the LCG films were irradiated with UV light below Tg, changes in the microscopic surface morphology were observed, while no appreciable macroscopic change was observed. On the other hand, when the LCGs were plasticized by suspending in solvents or heating above Tg, the LCG films showed macroscopic changes (e.g. bending) upon UV light irradiation. The bending and unbending could be repeated just by changing the wavelength of the irradiation light. It was suggested that the bending is induced by an absorption gradient which produces a volume difference between the front surface area and the bulk of the gel films. [ABSTRACT FROM AUTHOR]

Azobenzene liquid-crystalline (LC) polymers coated on a flexible polymer substrate were directly crosslinked by electron beams (EBs). We demonstrated that EB-crosslinked azobenzene LC polymers could successfully work as photomobile polymer materials with an adhesive-free bilayer structure. [ABSTRACT FROM AUTHOR]

The composition of a crosslinked azobenzene liquid-crystalline polymer and a flexible polymer film can provide a variety of simple devices that can walk in one direction like an ‘inchworm’ and move like a ‘robotic arm’ induced by light. [ABSTRACT FROM AUTHOR]

Freestanding crosslinked liquid-crystalline polymer films obtained by self-assembly through intermolecular hydrogen bonding showed photoinduced bending and unbending. The structural change at the microscopic level, caused by trans–cis photoisomerization of the azobenzene moieties at the hydrogen-bonded crosslinks, is successfully converted into a macroscopic deformation in the liquid-crystalline polymer films. [ABSTRACT FROM AUTHOR]

A foreword to the journal "Molecular Crystals and Liquid Crystals," is presented.