Sum-frequency spectroscopy of a monolayer of zinc arachidate at the solid-solid interface

Infrared-visible sum-frequency spectroscopy has been used to record the vibrational spectrum of a zinc arachidate monolayer at the interface between a sapphire prism and a fused silica lens. Spectra have been recorded for the monolayer deposited on the prism before, during, and after contact, and as a function of increasing pressure. Sum-frequency spectra are reported of the monolayer under sliding contact. The monolayer is found to be resistant to pressure- and shear-induced conformational disorder. However, frequency shifts, drops in peak intensities, and changes in peak intensity ratios have been observed as the monolayer is placed in contact between the prism and the lens. Transfer of monolayer material between the two surfaces is observed and is confirmed by spectra obtained with a monolayer deposited on the surface of the lens rather than the prism. On one face of the sapphire prism, the monolayer reconstructs to a low symmetry layer, probably due to epitaxy. The epitaxial structure disappeared in contact. Existing models for calculating sum-frequency spectra have been extended to include unit cells containing two molecules and torsion about the terminal C-C bond. This model can explain some, but not all, of the experimental observations.     

14‐Vertex Heteroboranes with 14 Skeletal Electron Pairs: An Experimental and Computational Study

Three isomers of [(Cp*Ru)₂C₂B₁₀H₁₂], the first examples of 14‐vertex heteroboranes containing 14‐skeletal electron pairs, have been synthesized by the direct electrophilic insertion of a {Cp*Ru⁺} fragment into the anion [4‐Cp*‐4,1,6‐RuC₂B₁₀H₁₂]^?. All three compounds have the same unique polyhedral structure having an approximate C_s symmetry and featuring a four‐atom trapezoidal face. X‐ray diffraction studies could confidently identify only one of the two cage C atoms in each structure. The other C atom position has been established by a combination of i) best fitting of computed and experimental ¹¹B and ¹H NMR chemical shifts, and ii) consideration of the lowest computed energy for series of isomers studied by DFT calculations. In all three isomers, one cage C atom occupies a degree‐4 vertex on the short parallel edge of the trapezium.     

Microanalytical isotope ratio measurements and elemental mapping using laser ablation ICP-MS for tissue thin sections: zinc tracer studies in rats

The kinetics of zinc absorption, metabolism and excretion is extensively studied by nutritionists. Stable isotopes of zinc can be used to identify body zinc compartments that have different turnover kinetics. Since the compartments might belong to physiological subsections of different organs, there is a need for microsampling analysis to determine isotope ratios of the trace element zinc in tissue samples. Here, we study the feasibility to use laser ablation coupled to quadrupole ICP-MS for the determination of zinc tracers given to rats at different time points with the aim to generate isotope ratio bioimages of heart tissue. A double tracer (⁷⁰Zn and ⁶⁷Zn) experiment with rats was designed to label the exchangeable zinc pool as well as the stable zinc pool. The isotope ratios determined by laser ablation ICP-MS were evaluated by additional measurements of tissue digests. Accumulated tracers which made up more than 0.1% of total zinc could be identified in the tissues of the treated rats. It was established that at least 50 measurements from the microsampling were necessary to distinguish between controls and a tracer treated rat resulting in reduced resolution of the bioimage. With the parameters used, features in the tissue thin sections of at least 250 μm² in size are necessary to detect the incorporation of a tracer. When different time points have to be measured, higher precisions are required and therefore a larger area needs to be ablated (1 mm²). Using the bioimages and pool measurements from one physiological feature, it was possible to show that the aorta cell walls incorporate the zinc tracer at the different time points.     

On the Antipode of a Co-Frobenius (Co)Quasitriangular Hopf Algebra

For H a quasitriangular Hopf algebra, S ², the square of the antipode is the inner automorphism induced by the Drinfeld element u, and S ⁴ is the inner automorphism induced by the grouplike element g = uS(u)^?1. For H finite dimensional, results of Drinfeld and Radford express g in terms of the modular elements of H. This note supplies another proof which replaces the requirement of finite dimensionality with existence of a nonzero integral for H in H*. Similar results hold for the infinite dimensional coquasitriangular case; here we supply some interesting examples.     

Synthesis of 2-C-Fluoromethyl-Myo-Inositol

Synthesis of 2-C-fluoromethyl-myo-inositol from DL-l-O-benzyl-2-oxiranyl-3, 4, 5, 6-tetra-O-benzyl-myo-inositol is described.     

On the continuity of separately continuous bihomomorphisms

Separately continuous bihomomorphisms on a product of convergence or topological groups occur with great frequency. Of course, in general, these need not be jointly continuous. In this paper, we exhibit some results of Banach-Steinhaus type and use these to derive joint continuity from separate continuity. The setting of convergence groups offers two advantages. First, the continuous convergence structure is a powerful tool in many duality arguments. Second, local compactness and first countability, the usual requirements for joint continuity, are available in much greater abundance for convergence groups.