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Biomedical subjects

Georg H Mehl

Publications and source records attributed to Georg H Mehl.

14 recordsLinked to original sources

Design of mesomorphic diarylethene-based photochromes.

The effects of the molecular variation of diarylethenes on the mesomorphic, photochromic, and fluorescence properties have been investigated, and dramatic changes in the fluorescence, photochromic, and liquid crystal behavior were observed.

Journal Article↗

Modulation of the absorption, fluorescence, and liquid-crystal properties of functionalised diarylethene derivatives.

Systematic variation of the molecular symmetry in a photochromic system based on a 1,2-bis(2-methylbenzo[b]thiophen-3-yl)hexafluorocyclopentene group, connected by decyl spacers to two cyanobiphenyl groups as mesogens, allows for a systematic investigation of the correlations between molecular shape and symmetry, electronic effects, photochromic conversion and liquid-crystalline properties.

Calorimetry, Differential Scanning↗

Full miscibility of disk- and rod-shaped mesogens in the nematic phase.

Mesogens containing rod-shaped moieties as well as one disk-shaped group exhibit nematic phase behavior and are entirely miscible with rod- and disk-shaped mesogens in the nematic phase. In the phase diagram, an extra nematic phase appears at nearly equimolar disk-rod ratios, where the nematic biaxial phase has been predicted.

Journal Article↗

Self-organizing properties of natural and related synthetic glycolipids.

In this article we report on the syntheses, self-organizing properties, and structures of a variety of cerebrosides and related synthetic glycolipids. The thermotropic and lyotropic liquid crystalline properties of the materials were evaluated in detail. All of the families of materials studied exhibited columnar mesophases. In the dry state the aliphatic chains were found to be located on the exterior of the columns, whereas in the wet state the reverse was the case with the polar headgroups on the exterior. Thus, the aliphatic chains act almost like hydrocarbon solvents in the dry state.

Cerebrosides↗