Simple chiral urea gelators, (R)- and (S)-2-heptylurea: their gelling ability enhanced by chirality.

We present the first report on the synthesis of chiral ureas, (R)- and (S)-2-heptylurea, and their gelling behaviors. The ureas were prepared by the reactions of chiral amines and phenyl carbamate in the presence of triethylamine. On cooling from homogeneous solutions, the chiral ureas form gels in water and various nonpolar organic solvents, such as cyclohexane, toluene, and tetrachloromethane, while the racemate gelatinize only toluene and tetrachloromethane among the solvents we examined.

Liquid crystalline elastomers as actuators and sensors.

This review collects recent developments in the field of liquid crystalline elastomers (LCEs) with an emphasis on their use for actuator and sensor applications. Several synthetic pathways leading to crosslinked liquid crystalline polymers are discussed and how these materials can be oriented into liquid crystalline monodomains are described. By comparing the actuating properties of different systems, general structure-property relationships for LCEs are obtained.

Gelling and the collective dynamics in ferroelectric liquid crystals.

Dielectric spectroscopy has been applied to investigate the dynamic behaviour of a ferroelectric liquid crystal in the smectic C* and smectic A phases confined in gel matrices of a fibre like (1D) or platelet like (2D) structure. These gel matrices were obtained from semicarbazide or bis-acylurea derivatives, which self assemble because of their H-bonding motif. The confinement strongly influences the magnitude of the spontaneous polarization and the collective fluctuations of the director detected as the Goldstone-mode.

Physicochemical characterization of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines non-covalently incorporated into an organogel and their remarkable morphological effect on the nanoscale-fibers.

A series of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines were efficiently incorporated into an organogel made of (1R,2R)-trans-1,2-bis(dodecanoylamino)cyclohexane by means of multiple cooperative non-covalent interactions, and SEM revealed the formation of unique brush-like nanostructures.