Solid-state one-way photoisomerisation of Z,E,Z-1,6-(4,4'-diphenyl)hexa-1,3,5-triene dicarboxylate examined using higher-order derivative spectra and powder XRD patterns.

Higher order derivative spectra were applied at first to one-way ZEZ-to-EEE photoisomerisation of dimethyl ester (ZEZ-DPH1) of the titled compound in a methylcyclohexane solution. Many common crossing points emerged in UV-induced derivative-spectral changes to reveal the direct ZEZ-to-EEE photoisomerisation without the transient formation of an intermediate to suggest the bicycle-pedal mechanism. The solid-state photoisomerisation was subsequently monitored by tracing changes in the fourth-order derivatives of absorption spectra of a thin crystalline layer of ZEZ-DPH1 prepared by the drop-casting method, because the distortion of absorption spectra due to light scattering is cancelled. It was suggested that the solid-state photochemical event consists of three steps: fast ZEZ-to-EEE photoisomerisation, a subsequent slow ZEZ-to-EEE photoisomerisation and very slow disappearance of the EEE-isomer. Studies on powder XRD were also carried out for a drop-cast solid layer of ZEZ-DPH1 to disclose the coexistence of a crystal form other than the original one, and the former exhibited faster ZEZ-to-EEE photoisomerisation when compared with the original crystal form. The results revealed by XRD analysis are in line with those obtained by higher-order derivative spectra, confirming the solid-state one-way photoisomerisation to take place through the bicycle-pedal process.

Photoisomerisation of azobenzene crystals in aqueous dispersions examined by higher order derivative spectra.

Photo-induced UV-Vis spectral changes of azobenzene (Az) in solution and aqueous crystalline dispersions were analysed by means predominantly of fourth order derivatives. Weak bands due to vibration level transitions (VLT) of E-isomers in solution were well-resolved in derivatives to estimate conversion of photoisomerisation by tracing extrema of a VLT sub-peak. The photo-induced derivative-spectral changes of Az crystals dispersed in aqueous PVA solutions generated many common crossing points to indicate that Az dissolves partially in a PVA solution to lead to photoisomerisation in a homogeneous phase and the reversible alteration of particle size. The solid-state photoisomerisation of Az was investigated by the preparation of PVA-free aqueous dispersions of powdery nanohybrids comprised of Az and silica nanoparticles. The fourth order derivatives of spectral changes revealed that the photochemical process involves three kinds of species including non-aggregated and aggregated E-isomers as well as Z-isomers.

Solid-state photoelectron transfer in powdery nanocomposites comprised of a sensitiser, photoacid generators and silica nanoparticles.

The dry beads milling of a mixture of 9,10-dipropoxyanthracene (DPA) as an electron donor and surface-modified silica nanoparticles was conducted in the absence or in the presence of a photoacid generator (PAG) as an electron acceptor to give powdery nanocomposites. Fluorescence measurements indicated no mechanochemical change in the crystal structure of DPA after the nanohybridisation. The co-milling with PAG resulted in solid-state fluorescence quenching, whereas quenching efficiency was considerably dependent on the nature of PAG. The solid-state sensitised photoacid generation through the electron transfer was demonstrated by the solid-state photocolouration of leuco-dye of crystal violet lactone.

Highly sensitive photoalignment of calamitic and discotic liquid crystals assisted by axis-selective triplet energy transfer.

Highly sensitive photoalignment of liquid crystals (LCs) can be realized by axis-selective triplet energy transfer. Addition of a triplet photosensitizer (phosphorescent donor) into a photocrosslinkable polymer tethering E-cinnamate side chains ensures dramatic enhancement of photosensitivity to generate the optical anisotropy of polymer film and surface-assisted LC photoalignment. Photoirradiation of triplet photosensitizer-doped polymer films with linearly polarized 365 nm light for the selective excitation of triplet sensitizer gives rise to optical anisotropy of cinnamates as a result of axis-selective triplet energy transfer. By analyzing phosphorescence spectra with theoretical Perrin's formula, we find that triplet energy transfer is efficient within a radius of ∼0.3 nm from the triplet photosensitizer. Such photoaligned polymer films can be used for the surface-assisted orientation photocontrol of not only calamitic LC, but also discotic LC, even for extremely low exposure energies. The present procedure would be greatly advantageous for high-throughput fabrication of optical devices by photoalignment techniques.

Photoisomerisation behaviour of azobenzene crystals hybridised with silica nanoparticles by dry grinding.

The dry grinding of azobenzene crystals with silica nanoparticles gave nanohybrids, which exhibited reversible photoisomerisation in water through linearly consecutive processes. The hybrids mill-dispersed in an aqueous PVA solution displayed different spectral changes due to the partial dissolution of azobenzene in PVA coils in water.

Reversible photoisomerisability and particle size changes of mill-dispersed azobenzene crystals in water.

Azobenzene crystals exhibited E/Z photoisomerisability at a level of ca. 30%, accompanied by particle size changes, when they were milled in water to fabricate submicron-sized particles.

Core-shell structures of silica-organic pigment nanohybrids visualized by electron spectroscopic imaging.

Energy-filtering electron transmission spectroscopy observation has been achieved to elucidate the nanostructures of powdery nanohybrids, which were produced by the dry mechanical milling of organic pigments and silica nanoparticles. The hybrids possess core-shell structures, irrespective of the levels of aggregation of primary particles, whereas hollow sites of aggregates of primary silica particles were filled with the pigment, leading to the locally concentrated distribution of the pigment to reduce the surface areas of the hybrids. The results imply that nanohybridization is referred to as the buildup method, although mechanical tools and procedures are quite the same as those for the conventional breakdown method.

Solid phase adsorption of crystal violet lactone on silica nanoparticles to probe mechanochemical surface modification.

The solid phase adsorption of crystal violet lactone (CVL) on five types of Stober silica nanopowders with BET specific surface areas in the range of 50-800 m2/g under dry milling conditions was described for the first time. The hydrogen bonding between surface silanol and the carboxylate of the ring-opened triphenylmethane dye (CVL+) led to the formation of monolayers of CVL+ in a flat-laid configuration. The lambda max of CVL+ in diffusive reflection visible spectra was influenced by the particle size of silica powders, suggesting that the microenvironmental polarity of adsorbed CVL+ is considerably reduced along with the decrease of the particle size. The solid phase adsorption of CVL obeyed Langmuir adsorption isotherms to give a saturated amount of CVL+ for every silica nanoparticle. The surface concentration of CVL+ on nanoparticles at the saturation was estimated to be 0.31 mg/m2 on average, disclosing that about 52% of the surface can be covered by CVL+ under the assumption that the BET-specific surface areas are equivalent to the real surfaces active for the CVL adsorption. The generation of the blue color of CVL provided a convenient means to estimate qualitative and quantitative analysis of the surface coverage with surface-active reagents, which conceal surface silanols. Subsequently, silica nanoparticles were milled with a surface modifier, followed by milling with CVL to observe the intensity of the blue color in order to disclose that the surface coverage with oligo- and polyethylene glycols as well as with nonionic surfactants by dry milling was specifically determined by the number of repeating oxyethylene units. Although the surface-active reagents were easily desorbed in water, the desorption was notably suppressed by milling with CVL, suggesting that the surface-modified particles with the surface-active reagents are covered with ultrathin films of CVL.

Surface-assisted photoalignment of discotic liquid crystals by nonpolarized light irradiation of photo-cross-linkable polymer thin films.

In this article, we describe the surface-assisted photoalignment of discotic liquid crystals (DLCs) on thin films of photo-cross-linkable polymers with cinnamoyl moieties as the side chains. Oblique irradiation of the polymer thin films with nonpolarized UV light at 313 nm brought about inclined orientation of the cinnamoyl residues as a result of their direction-selective photoisomerization and photodimerization. The DLC molecules on the photoirradiated polymer films were aligned in a tilted hybrid manner. This means that the DLC directors are continuously altered from the substrate to the DLC film surface so as to minimize the elastic free energy. Interestingly, we found that the tilted direction of aligned DLC molecules is clearly influenced by the chemical structures of the cinnamate-containing polymers. When a poly(vinyl cinnamate) thin film was obliquely exposed to nonpolarized UV light, the DLCs were inclined to the direction opposite to the UV light propagation. In a keen contrast, the thin film of poly(methacrylate)s tethering cinnamoyl groups, which was obliquely exposed to nonpolarized UV light in advance, provided the tilting DLC direction in parallel with the light propagation. The results were supported by tilted orientation of calamitic (rod-shaped) liquid crystal on the obliquely irradiated polymer films. Such photoalignment behavior of the DLCs can be rationalized by anchoring balance between intermolecular interaction of the DLC molecules with the photodimers of polymer films and those with the remaining E-isomers of cinnamoyl side chains at the film interface. The present technique of DLC photoalignment opens promising ways not only to understand anisotropic physical properties of DLCs, but also to design and fabricate novel nanodevices for photonics and electronics applications.

Surface-mediated photoalignment of discotic liquid crystals on azobenzene polymer films.

This paper describes a simple strategy for the formation of photoaligned and micropatterned discotic liquid crystal (DLC) film on the surface of photoirradiated azobenzene-containing polymer thin film. The key material for the surface-mediated photoalignment of the DLCs was poly[4-(4-cyanophenylazo)phenyl methacrylate] (pMAzCN). Optical anisotropy was generated in a pMAzCN film by oblique exposure to nonpolarized light which resulted in angle-selective photoisomerization and reorientation of the azobenzenes. Subsequent annealing of the film at 240 degrees C enhanced the photoaligned state of the p-cyanoazobenzenes due to strong intermolecular dipole-dipole interaction and semicrystalline nature of the pMAzCN. This combination of photoirradiation and subsequent annealing of the pMAzCN film made it possible to realize the surface-assisted orientation control of a DLC molecule, which displays both columnar (Col) and discotic nematic (N(D)) phases over 152 degrees C. When the pMAzCN film was exposed to linearly polarized light from the surface normal, the DLC molecules showed homeotropic orientation with the director perpendicular to the substrate surface. In the contrast, oblique irradiation of the pMAzCN film with nonpolarized light gave rise to tilted DLC orientation with well-ordered optical birefringence at the N(D) phase. Rapid cooling from the N(D) phase produced a well-aligned glassy N(D) state at room temperature, which was adequately stable for 10 months even though no covalent cross-linking among the DLCs was performed. The spatial orientation of photoaligned DLCs in both their bulk film and in their interface region was characterized by means of optical birefringence, X-ray diffraction, and fluorescence measurements. At the N(D) phase, the DLC molecules were aligned in a hybrid manner such that their tilt angles varied throughout the thickness of DLC film. The direction of tilted DLCs was opposite to the propagation of the actinic nonpolarized light. The photoaligned DLC films exhibited polarized fluorescence emission with an s-polarized/p-polarized intensity ratio of 4.1, despite the nonpolarized excitation of only DLC at outmost surface. These results indicate that the three-dimensionally aligned azobenzene moieties of the pMAzCN thin film were transferred to the tilted DLC molecules at air/DLC interface. Finally, we demonstrated micrometer-scale photopatterned orientation of DLC molecules on the pMAzCN surface by oblique nonpolarized irradiation of the film through a photomask.

Optical and surface morphological properties of polarizing films fabricated from a chromonic dye by the photoalignment technique.

The inherent chromonic lyotropic liquid crystalline properties of a dye have been manipulated to fabricate multi-axial micropolarizing thin films by means of the photoalignment technique. The dye aqueous solution is deposited on a photopatterned polymer film to result in the macroscopic alignment of the dye molecules, followed by drying at ambient temperature. The solid polarizing dye layers thus produced exhibit very a high contrast ratio and degree of polarization in the region of visible light. Addition of a small amount of surfactant to the dye solution is a prerequisite for the generation of a nematic chromonic phase and for the formation of homogeneous thin dye layers on the polymer film. The correlation between the optical and surface morphological properties of the dye layers is discussed.

Nonlinear organic reactions to proliferate acidic and basic molecules and their applications.

Acid amplifiers derived from a certain class of sulfonates suffer from autocatalytic decomposition in the presence of a strong acid to give corresponding sulfonic acids, which catalyze the decomposition of the parent sulfonates, leading to the liberation of more of the same sulfonic acids in an exponential manner. Five types of acid amplifiers displaying acid proliferation reactions are presented. A certain type of carbamate exhibits autocatalytic fragmentation to give the corresponding aliphatic amine and olefin together with carbon dioxide, whereas the generated amine is able to act as a catalyst for the fragmentation so that the carbamates are referred to as base amplifiers. Applications of acid and base amplifiers to photofunctional materials, including photoresists, are described as a consequence of the combination of the molecular amplifiers with photoacid as well as photobase generators. Practical applications of acid proliferation reactions in polymer films are discussed.

Holographic Bragg gratings in a photoresponsive cross-linked polymer-liquid-crystal composite.

Holographic gratings were in a composite material that comprised a cross-linked polymer with azobenzene side chains and a nematic liquid crystal. Holographic recording was based on the photoinduced alignment of the nematic liquid crystal inside a cell as a result of amplification of the photoreorientation of azobenzene residues. The diffraction efficiency depends on cell thickness and reading angle of the gratings, so this composite material exhibits volume holographic properties with Bragg diffraction.