Plasmonic metamaterial wave retarders in reflection by orthogonally oriented detuned electrical dipoles

We demonstrate that a pair of perpendicular electrical dipolar scatterers resonating at different frequencies can be used as a metamaterial unit cell to construct a nanometer-thin retarder in reflection, designing nanocross and nanobrick plasmonic configurations to function as reflecting quarter-wave plates at ~1520 and 770 nm, respectively. The design is corroborated experimentally with a monolayer of gold nanobricks, transforming linearly polarized incident radiation into circularly polarized radiation at ~780 nm.     

Porous-core honeycomb bandgap THz fiber

In this Letter we propose a novel (to our knowledge) porous-core honeycomb bandgap design. The holes of the porous core are the same size as the holes in the surrounding cladding, thereby giving the proposed fiber important manufacturing benefits. The fiber is shown to have a 0.35-THz-wide fundamental bandgap centered at 1.05?THz. The calculated minimum loss of the fiber is 0.25?dB/cm.     

Microcrystallography, high-pressure cryocooling and BioSAXS at MacCHESS

The Macromolecular Diffraction Facility at the Cornell High Energy Synchrotron Source (MacCHESS) is a national research resource supported by the National Center for Research Resources of the US National Institutes of Health. MacCHESS is pursuing several research initiatives designed to benefit both CHESS users and the wider structural biology community. Three initiatives are presented in further detail: microcrystallography, which aims to improve the collection of diffraction data from crystals a few micrometers across, or small well diffracting regions of inhomogeneous crystals, so as to obtain high-resolution structures; pressure cryocooling, which can stabilize transient structures and reduce lattice damage during the cooling process; and BioSAXS (small-angle X-ray scattering on biological solutions), which can extract molecular shape and other structural information from macromolecules in solution.     

Electrochemical characterization of hydrogels for biomimetic applications

Hydrogels are increasingly being recognized as having potential in bio‐compatible applications. In previous work, we investigated the feasibility of poly(ethylene glycol)‐dimethacrylate (PEG‐1000‐DMA) and poly(ethylene glycol)‐diacrylate (PEG‐400‐DA) polymerized using either a chemical initiator (C) or a photoinitiator (P) to encapsulate and stabilize biomimetic membranes for novel separation technologies or biosensor applications. In this paper, we have investigated the electrochemical properties of the hydrogels used for membrane encapsulation. Specifically, we studied the crosslinked hydrogels by using electrochemical impedance spectroscopy (EIS), and we demonstrated that chemically crosslinked hydrogels had lower values for the effective electrical resistance and higher values for the electrical capacitance compared with hydrogels with photoinitiated crosslinking. Transport numbers were obtained using electromotive force measurements and demonstrated that at low salt concentrations, both PEG‐400‐DA‐C and PEG‐400‐DA‐P hydrogels presented an electropositive character whereas PEG‐1000‐DMA‐P was approximately neutral and PEG‐1000‐DMA‐C showed electronegative character. Sodium transport numbers approached the bulk NaCl electrolyte value at high salt concentrations for all hydrogels, indicating screening of fixed charges in the hydrogels. The average salt diffusional permeability 〈P_s〉 and water permeability 〈P_w〉 were found to correlate with EIS results. Both PEG‐1000‐DMA‐C and PEG‐400‐DA‐C had higher 〈P_s〉 and 〈P_w〉 values than PEG‐1000‐DMA‐P and PEG‐400‐DA‐P hydrogels. In conclusion, our results show that hydrogel electrochemical properties can be controlled by the choice of polymer and type of crosslinking used and that their water and salt permeability properties are congruent with the use of hydrogels for biomimetic membrane encapsulation. Copyright © 2011 John Wiley & Sons, Ltd.     

Optimization over geodesics for exact principal geodesic analysis

In fields ranging from computer vision to signal processing and statistics, increasing computational power allows a move from classical linear models to models that incorporate non-linear phenomena. This shift has created interest in computational aspects of differential geometry, and solving optimization problems that incorporate non-linear geometry constitutes an important computational task. In this paper, we develop methods for numerically solving optimization problems over spaces of geodesics using numerical integration of Jacobi fields and second order derivatives of geodesic families. As an important application of this optimization strategy, we compute exact Principal Geodesic Analysis (PGA), a non-linear version of the PCA dimensionality reduction procedure. By applying the exact PGA algorithm to synthetic data, we exemplify the differences between the linearized and exact algorithms caused by the non-linear geometry. In addition, we use the numerically integrated Jacobi fields to determine sectional curvatures and provide upper bounds for injectivity radii.     

SPEKTROSKOPISCHE SUBSTITUENTENKONSTANTEN,VI SYNTHESE UND UV-SPEKTREN VON 4-PIPERIDINO-PHENYL-PHOSPHOR-VERBINDUNGEN

Abstract

Triarylphosphines containing 4-piperidinophenyl rings are conveniently prepared by PO-activated nucleophilic aromatic substitution of fluorine by piperidine and subsequent reduction of the phosphine oxides. The UV spectra of the 4-piperidinophenyl-phosphorus compounds closely resemble those of the analogous dimethylanilines. Spectroscopic substituent constants are obtained by application of the Doub-Vandenbelt equation.

Triarylphosphine mit 4-Piperidinophenyl-Ringen sind durch PO-aktivierte nukleophile aromatische Substitution von Fluor durch Piperidin bequem zugänglich; die Phosphine entstehen durch Reduktion der Phosphinoxide. Die UV-Spektren der 4-Piperidinophenyl-phosphor-Verbindungen sind denen der analogen Dimethylaniline sehr ähnlich. Mit Hilfe der Doub-Vandenbelt-Gleichung werden spektroskopische Substituentenkonstanten gewonnen.     

Shifted-basis technique improves accuracy of peak position determination in Fourier transform mass spectrometry

The present paper suggests a new algorithm for estimation of peak positions in FTMS spectra. It is shown theoretically and experimentally that the new technique yields superior results compared to the currently applied techniques, when the noise level is high and/or the peaks are located close to each other. Cases are presented where the deviation from the true mass could be mistaken for space charge effect, while the shift is in fact solely due to the shortcomings of the current techniques and can be corrected by applying the shifted-basis technique. In two out of three cases, this technique gave more accurate (>5 times) result compared to the conventional analysis. In the third case, where the signal was high compared to the noise, the results were comparable. The new technique can be used to achieve better mass accuracy for noisy and not well resolved spectra, and to further investigate the features of the space charge effect.     

Pharmazeutische Pr?parate

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Untersuchungen zur Topologie der geschlossenen zweiseitigen Flächen

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