Directed self-assembly of a helical nanofilament liquid crystal phase for use as structural color reflectors

The fabrication of molecular structures with a desired morphology, e.g., nanotubes, nanoribbons, nanosprings, and sponges, is essential for the advancement of nanotechnology. Unfortunately, realization of this objective is expensive and complicated. Here, we report that irradiating a film comprising azobenzene derivatives with UV light produces oriented arrays of helical nanofilaments via the photoisomerization-induced Weigert effect. As a result, structural colors are observed due to the extrinsic chiral reflection in the visible wavelength range, and the reflected color can be tuned by adjusting the molecular length of the azobenzene derivative. This simple fabrication method can be used for fabricating large, reversible, and patternable color reflectors, providing a new platform for interference-based structural coloration as it exists in nature, such as morpho butterflies, green-winged teal, and various beetles

Stimuli Thresholds for Isomerization-Induced Molecular Motions in Azobenzene-Containing Materials.

We use large-scale molecular dynamics simulations of the isomerizations of azobenzene molecules diluted inside a simple molecular material to investigate the effect of a modification of the cis isomer shape on the induced diffusion mechanism. To this end we simulate incomplete isomerizations, modifying the amplitude of the trans-to-cis isomerization. We find thresholds in the evolution of the host molecules mobility with the isomerization amplitude, a result predicted by the cage-breaking mechanism hypothesis (Teboul, V.; Saiddine, M.; Nunzi, J. M.; Accary, J. B. J. Chem. Phys. 2011, 134, 114517) and by the gradient pressure mechanism theory (Barrett, C. J.; Rochon, P. L.; Natansohn, A. L. J. Chem. Phys. 1998, 109, 1505–1516.). Above the threshold the diffusion then increases linearly with the variation of the chromophore size induced by the isomerization

Effects of particle distribution on mechanical properties of magneto-sensitive elastomers in a homogeneous magnetic field

We propose a theory which describes the mechanical behaviour of magneto-sensitive elastomers (MSEs) under a uniform external magnetic field. We focus on the MSEs with isotropic spatial distribution of magnetic particles. A mechanical model is used in which magnetic particles are arranged on the sites of three regular lattices: simple cubic, body-centered cubic and hexagonal close-packed lattices. By this we extend our previous approach [Ivaneyko D. et al., Macromolecular Theory and Simulations, 2011, <b>20</b>, 411] which used only a simple cubic lattice for describing the spatial distribution of the particles. The magneto-induced deformation and the Young's modulus of MSEs are calculated as functions of the strength of the external magnetic field. We show that the magneto-mechanical behaviour of MSEs is very sensitive to the spatial distribution of the magnetic particles. MSEs can demonstrate either uniaxial expansion or contraction along the magnetic field and the Young's modulus can be an increasing or decreasing function of the strength of the magnetic field depending on the spatial distribution of the magnetic particles

Copper-catalyzed dehydrogenative polycondensation of a bis-aniline hexylthiophene-based monomer : a kinetically controlled air-tolerant process

Aerobic oxidative dehydrogenative polycondensation of the new monomer 4,4'-(3-hexylthiophene-2,5-diyl)bis(2-octylaniline) has proved very effective under mild conditions using an inexpensive copper bromide/pyridine complex and dioxygen acting as catalyst and oxidant, respectively. Such kinetically controlled process allowed preparing elec-troconjugated photosensitive polymers with high molar weight (Mn > 15000 g.mol-1)