Surface grafted agents with various molecular lengths and photochemically active benzophenone moieties.

Homologues of benzophenone silane, a covalently graftable, photochemically active surface functionalizing agent, are investigated as surface functionalization agents for both small particles and planar substrates. In these homologues, a chlorosilane functional group and a photochemically active benzophenone oxo moiety are separated with an aliphatic spacer of varying length. The species obtained are first investigated by surface grafting on substrates (Si wafers, glass plates, and indium tin oxide coated glass plates). Si wafer samples are investigated with ellipsometry clearly indicating monolayer formation. The monolayer thickness can be controlled by the size of the aliphatic spacer group and also by the doping concentration of the solution used in the spin-casting step. The functionalized surfaces are further investigated by measuring the contact angle of a suitable organic fluid, a nematic liquid crystal. Photo exposure of these samples results in a drastically varied contact angle: The surface grafted species are still photochemically active and photo exposure leads to the addition of a nearby organic molecule (from the liquid crystalline phase) to each activated surface agent molecule. The synthesized species are then investigated as (covalently binding) surfactants in the wet planetary ball milling process aimed to fabricate solid-liquid dispersions (of Fe doped lithium niobate particles). It was found that the use of species with higher molecular length results in dispersions of small particles, functionalized with photochemically active surface agents. Indeed, they show better performance than conventional surfactants.

Adaptive high-resolution Linnik interferometry for 3D measurement of microparticles.

Tailored 3D microparticles and nanostructures lead to increasing possibilities in semiconductor industry or biomedical applications. In an interdisciplinary study we investigate the parallel production of such particles by using nanoimprint lithography in combination with their characterization based on interference microscopy. In this Letter we report on a metrological inspection, which tends to a universal measurement solution comparing the sample optically to a master object produced in the same way as the sample.

Generation of twisted nanowires with achiral organic amphiphilic copper complexes.

Drying under solvent atmosphere (DUSA) was investigated as an experimental technique to generate self-assembled nanowires and needles from solutions of organic molecules under controlled conditions. Experimental observations of twisted nanowires are reported. These twisted nanowires were obtained by drying of solutions of achiral molecules under solvent controlled atmospheres: achiral, amphiphilic copper complexes were dissolved in an achiral solvent and these solutions were dried under controlled conditions. Two structurally related copper complexes were investigated. Microscopic investigations of the resulting nanowires revealed, and scanning electron microscopy confirmed: self-assembled twisted ribbons could be selectively obtained from one of these compounds. This behavior could be explained by comparing the ratio of the size of the head group and the overall length of the molecules. The occurrence of chiral filaments and chiral phases of nanosegregated filaments are rare in achiral compounds. The occurance of such twisted filaments is thought to be related to symmetry-breaking during a phase transition from liquid crystalline or lyotropic liquid crystalline phases to a nanosegregated phase. In the reported experiments, the concentration of a solution was gradually increased until crystallization occurred. The results clearly show how DUSA can be applied to investigate the capability of achiral substances to yield twisted filaments. Moreover, the investigated compounds had high-enough charge carrier mobilities, such that the twisted filaments obtained are candidates for self-assembled, intrinsically coiled nano-inductivities.

Coordination Polymers based on the Neutral Ditopic Ligand (C6H4PO(OCH3)2)2 Involving some f-Block Elements.

An improved synthesis using microwave heating affords (C6H4PO(OCH3)2)2 in excellent isolated yield (95 %). The ligand properties of this bisphosphonateester were explored towards hard metal centers M2+ (M = Ca, UO2) and M3+ (M = La, Ce, Sm, Eu) resulting in coordination polymers, for which the reduction of ionic size of the central metal atom resulted in lower-dimensional structural motifs as opposed to higher dimensional networks obtained for the larger ions. All coordination polymers were characterized by single-crystal X-ray diffraction, IR spectroscopy, and combustion analysis. The ligand was furthermore characterized with multinuclear NMR spectroscopy.