No abstract

We present a structural study of the mesophases of three achiral bent-core compounds with azo and azoxy bonds. The study is based on textures observation and small-angle X-ray diffraction. It is found that the materials exhibit columnar and tilted smectic mesophases. Optical second-harmonic generation measurements are performed on aligned samples of one of the compounds, and the whole second-order susceptibility tensor is determined. Finally, some simple aspects of the photoisomerization of the materials are examined.

A liquid crystal material of bent-core molecules is investigated by means of optical texture observations, x-ray measurements, and miscibility studies. While the x-ray and miscibility data point towards a B2 phase, the texture is however unusual, showing optical isotropy and segregation in two domains with opposite gyrations. It is shown that the texture can be interpreted successfully in terms of a smectic-C(A)P(A) structure in small domains with random orientations. The optical activity data are also explained semiquantitatively.

An effective chemoenzymatic strategy is reported that has allowed the construction, for the first time, of a focused microarray of synthetic N-glycans. Based on modular approaches, a variety of N-glycan core structures have been chemically synthesized and covalently immobilized on a glass surface. The printed structures were then enzymatically diversified by the action of three different glycosyltransferases in nanodroplets placed on top of individual spots of the microarray by a printing robot. Conversion was followed by lectin binding specific for the terminal sugars. This enzymatic extension of surface-bound ligands in nanodroplets reduces the amount of precious glycosyltransferases needed by seven orders of magnitude relative to reactions carried out in the solution phase. Moreover, only those ligands that have been shown to be substrates to a specific glycosyltransferase can be individually chosen for elongation on the array. The methodology described here, combining focused modular synthesis and nanoscale on-chip enzymatic elongation, could open the way for the much needed rapid construction of large synthetic glycan arrays.