Automatic alignment of a Kirkpatrick-Baez active optic by use of a soft-x-ray Hartmann wavefront sensor

We present what we believe to be the first automatic alignment of a synchrotron beamline by the Hartmann technique. Experiments were performed, in the soft-x-ray range (E=3 keV, lambda=0.414 nm), by using a four-actuator Kirkpatrick-Baez (KB) active optic. A system imaging the KB focal spot and a soft-x-ray Hartmann wavefront sensor were used alternatively to control the KB optic. The beam corrected with the help of the imaging system was used to calibrate the wavefront sensor. With both closed loops, we focused the beam into a 6.8 microm x 9 microm FWHM focal spot.     

Motion of charged particles in a NUTty Einstein–Maxwell spacetime and causality violation

We investigate the motion of electrically charged test particles in spacetimes with closed timelike curves, a subset of the black hole or wormhole Reissner–Nordström-NUT spacetimes without periodic identification of time. We show that, while in the wormhole case there are closed worldlines inside a potential well, the wordlines of initially distant charged observers moving under the action of the Lorentz force can never close or self-intersect. This means that for these observers causality is preserved, which is an instance of our weak chronology protection criterion.     

High‐mobility solution‐processed zinc oxide thin films on silicon nitride

A high effective electron mobility of 33 cm² V^–1 s^–1 was achieved in solution‐processed undoped zinc oxide (ZnO) thin films. The introduction of silicon nitride (Si₃N₄) as growth substrate resulted in a mobility improvement by a factor of 2.5 with respect to the commonly used silicon oxide (SiO₂). The solution‐processed ZnO thin films grown on Si₃N₄, prepared by low‐pressure chemical vapor deposition, revealed bigger grain sizes, lower strain and better crystalline quality in comparison to the films grown on thermal SiO₂. These results show that the nucleation and growth mechanisms of solution‐processed films are substrate dependent and affect the final film structure accordingly. The substantial difference in electron mobilities suggests that, in addition to the grain morphology and crystalline structure effects, defect chemistry is a contributing factor that also depends on the particular substrate. In this respect, interface trap densities measured in high‐κ HfO₂/ZnO MOSCAPs were about ten times lower in those fabricated on Si₃N₄ substrates. (© 2014 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)

     

95 GHz millimeter wave signal generation using an arrayed waveguide grating dual wavelength semiconductor laser

We report the generation of a 95?GHz carrier frequency by optical heterodyning of two wavelengths from adjacent channels from an arrayed waveguide grating-based multiwavelength laser. The extended cavity structure of the device provides low phase noise and narrow optical linewidth, further enhanced by the intracavity filter effect of the arrayed waveguide grating. We demonstrate that the generated RF beat note, at 95?GHz, has a -3 dB linewidth of 250?kHz. To the best of our knowledge, this is the narrowest RF linewidth generated from a free-running dual-wavelength semiconductor laser. The device is realized as a photonic integrated circuit using active-passive integration technology, and fabricated on a multiproject wafer run, constituting a novel approach for a compact, low-cost dual-wavelength heterodyne source.     

Two additional 1,9-diarylnonanoid 3-glucosides from Erica cinerea among which an unusual α-dione in conformational equilibrium

Continuation of the phytochemical analysis of Erica cinerea fresh aerial parts resulted in the isolation of two new compounds with a very close chromatographic behavior. On the basis of spectroscopic evidence (UV, MS and NMR), the structures were established as (−)-(3S,6E)-1,9-bis(p-hydroxyphenyl)-3-hydroxynon-6-en-5-one 3-O-β-d-glucoside named 6,7-anhydroericaone 3-O-β-d-glucoside and (−)-(3S)-1,9-bis(p-hydroxyphenyl)-3-hydroxynonan-5,6-dione 3-O-β-d-glucoside named α-ericadione 3-O-β-d-glucoside. Unanticipated by its α-alkadione type structure —a very unusual feature in the plant kingdom— the latter metabolite was found as a mixture of the minor s-cis and the major s-trans conformers. Moreover, the GC-MS analysis of the aglycone moieties of such glucosides, pointed out the permanent absence of the molecular ion and the constant hydroxybenzylium base peak, as well as the conversion of the α-dione into the major α-keto-enol tautomer.     

On the gentle properties of anisotropic Besov spaces

In this paper, we prove that anisotropic homogeneous Besov spaces ${\stackrel{?}{B}}_{p,q}^{s,u}\left({\mathbb{R}}^d\right)$ are gentle spaces, for all parameters $s,p,q$ and all anisotropies $u$. Using the Littlewood–Paley decomposition, we study their completeness, separability, duality and homogeneity. We then define the notion of anisotropic orthonormal wavelet basis of $L^2\left({\mathbb{R}}^d\right)$, and we show that the homogeneous version of Triebel families of anisotropic orthonormal wavelet bases associated to the tensor product of Lemarié–Meyer (resp. Daubechies) wavelets are particular examples. We characterize the ${\stackrel{?}{B}}_{p,q}^{s,u}\left({\mathbb{R}}^d\right)$ spaces using Lemarié–Meyer wavelets. In fact, we show that these bases will be either unconditional bases or unconditional $1$-weak bases of ${\stackrel{?}{B}}_{p,q}^{s,u}\left({\mathbb{R}}^d\right)$, depending on whether ${\stackrel{?}{B}}_{p,q}^{s,u}\left({\mathbb{R}}^d\right)$ is separable or not. By introducing an anisotropic version of the class of almost diagonal matrices related to anisotropic orthonormal wavelet bases, we prove that these spaces are stable under changes of anisotropic orthonormal wavelet bases. As a consequence, we extend the characterization of ${\stackrel{?}{B}}_{p,q}^{s,u}\left({\mathbb{R}}^d\right)$ using Daubechies wavelets.     

The stable admissions polytope

The stable admissions polytope– the convex hull of the stable assignments of the university admissions problem – is described by a set of linear inequalities. It depends on a new characterization of stability and arguments that exploit and extend a graphical approach that has been fruitful in the analysis of the stable marriage problem. Received: April 10, 1998 / Accepted: June 3, 1999?Published online January 27, 2000     

The Inhibition of the Dissolution of Aluminium in Sodium Hydroxide by Some Organic Phosphorus Compounds

The inhibition of the corrosion of aluminium in 1M sodium hydroxide solution by some cyclodiphosphazane derivatives has been studied using hydrogen evolution technique. The results indicate that the additives reduce the corrosion rate. The inhibitory character of these compounds depends upon the concentration of the inhibitor, as well as on its chemical composition.     

Theoretical conformational analysis of opiate peptides Leu-Enkephalin (H-Tyr-Gly-Gly-Phe-Leu-OH) and its two thioamide analogs (H-Tyr-Glyψ[CSNH]Gly-Phe-Leu-OH) and (H-Tyr-Gly-Glyψ[CSNH]Phe-Leu-OH)

In order to find informations on the native structure of the Leu-Enkephalin opiate peptide, the parent peptide and its two thioamide analogs (Thio-Gly2)Leu-Enkephalin and (Thio-Gly3)Leu-Enkephalin were studied by the theoretical method PEPSEA. This comparative conformational analysis showed that the active conformation is a β turn structure centered on Gly3 and Phe4. Moreover, this study showed also that the more active analog (Thio-Gly2)Leu-Enk has a lower tendency to adopt this structure. Consequently, its high activity can only be explained by its long lifetime due to its resistance to enzymatic hydrolysis, following the substitution of the amide linkage by the thioamide one. The weakly active analog (Thio-Gly3)Leu-Enk does not adopt this structure and prefers instead a β turn structure centered on Gly2 and Gly3. This study also confirmed the importance of the distances between the Tyr and Phe residues at positions 1 and 4, and that of the terminal Tyrosine N-H group which must be free of any intramolecular hydrogen bond in order to be available in the molecular recognition process.