Wide view supertwisted nematic liquid-crystal light shutter

We present a novel concept of a wide viewing angle liquid-crystal display (LCD) light shutter, taking advantage of the highly symmetric 180 degrees -twisted liquid-crystal (LC) configuration and the light propagation starting with a single mode. In a specific case of the high voltage driven LCD light shutter, the resulting very high overall symmetry allows for the efficient angular compensation of the light attenuation in the optically closed state using just a simple, specifically tuned, negative-birefringent c-plate retarder. The latter can be adapted to compensate for the positive optical birefringence of the homeotropically aligned LC molecules as well as also for a great deal of the angular dependence of the crossed polarizers. We show that the additional partial compensation of the angular dependence of the crossed polarizers can be explained by a combined effect of the positive birefringence of the homeotropically aligned LC molecules, negative-birefringence c-plate retarder, and an in-plane residual positive birefringence (a-plate) of the boundary layers of the LC molecules.     

Measurement and Modeling of Water-Vapor Diffusion in Elastomers with Impact in Humidity and Vacuum Measurements

The dynamics of water-vapor dissolution in Viton O-rings is measured with a gravimetric method using a precise mass comparator. A sample gasket was degassed in high vacuum for a sufficiently long period to remove more than 99 % of the dissolved water vapor. After that, it was exposed to the ambient atmosphere with a controlled temperature, and relative humidity and water-vapor uptake curves were measured gravimetrically with a precise balance. The dynamics of a water-vapor release into vacuum from another sample that was previously saturated with water vapor at room temperature was determined. The sample was placed in a vacuum outgassing rate measurement apparatus. The time dependence of the evolved water vapor was calculated by integrating the measured outgassing rate. The physical process of water absorption can be described by the diffusion equation. The geometry of the samples required solving the diffusion equation in cylindrical coordinates. This was done numerically using a finite-difference method. As a result of the modeling, room temperature values of the diffusion constant $D$ D , the solubility $s$ s , and the permeability $K = D\times s$ K = D × s of water vapor in the sample material (Viton A-401C) were obtained. For sample 1, we obtained $D = 8.0 \times 10 ^{-8}$ D = 8.0 × 10 ? 8  cm $^{2}\,\,{\cdot }\,\,$ 2 · s $^{-1}$ ? 1 and $s = 6.5 \times 10^{-7}$ s = 6.5 × 10 ? 7  g $\,{\cdot }\,$ · cm $^{-3}\,{\cdot }\,$ ? 3 · Pa $^{-1}$ ? 1 , while for sample 2, $D = 3.0 \times 10^{-7}$ D = 3.0 × 10 ? 7  cm $^{2}\,{\cdot }\,$ 2 · s $^{-1}$ ? 1 and $s = 3.5 \times 10^{-7}$ s = 3.5 × 10 ? 7  g $\,{\cdot }\,$ · cm $^{-3}\,{\cdot }\,$ ? 3 · Pa $^{-1}$ ? 1 .     

Design,Synthesis, in vitro and in silico Characterization of 2-Quinolone-L-alaninate-1,2,3-triazoles as Antimicrobial Agents

Due to the ever-increasing antimicrobial resistance there is an urgent need to continuously design and develop novel antimicrobial agents. Inspired by the broad antibacterial activities of various heterocyclic compounds such as 2-quinolone derivatives, we designed and synthesized new methyl-(2-oxo-1,2-dihydroquinolin-4-yl)-L-alaninate-1,2,3-triazole derivatives via 1,3-dipolar cycloaddition reaction of 1-propargyl-2-quinolone-L-alaninate with appropriate azide groups. The synthesized compounds were obtained in good yield ranging from 75 to 80 %. The chemical structures of these novel hybrid molecules were determined by spectroscopic methods and the antimicrobial activity of the compounds was investigated against both bacterial and fungal strains. The tested compounds showed significant antimicrobial activity and weak to moderate antifungal activity. Despite the evident similarity of the quinolone moiety of our compounds with fluoroquinolones, our compounds do not function by inhibiting DNA gyrase. Computational characterization of the compounds shows that they have attractive physicochemical and pharmacokinetic properties and could serve as templates for developing potential antimicrobial agents for clinical use.     

Selective Monovalent Galectin-8 Ligands Based on 3-Lactoylgalactoside

Galectin-8 has gained attention as a potential new pharmacological target for the treatment of various diseases, including cancer, inflammation, and disorders associated with bone mass reduction. To that end, new molecular probes are needed in order to better understand its role and its functions. Herein we aimed to improve the affinity and target selectivity of a recently published galectin-8 ligand, 3-O-[1-carboxyethyl]-β-d -galactopyranoside, by introducing modifications at positions 1 and 3 of the galactose. Affinity data measured by fluorescence polarization show that the most potent compound reached a K_D of 12 μM. Furthermore, reasonable selectivity versus other galectins was achieved, making the highlighted compound a promising lead for the development of new selective and potent ligands for galectin-8 as molecular probes to examine the protein's role in cell-based and in vivo studies.     

Analysis of light scattering in amorphous Si:H solar cells by a one‐dimensional semi‐coherent optical model

A one‐dimensional semi‐coherent optical model for thin‐film solar cells is presented. The optical circumstances at flat interfaces are addressed and the situation at rough interfaces in the model is described for the case of direct (coherent) incident and scattered (incoherent) incident light. After the model has been experimentally verified, analysis of the light scattering process in hydrogenated amorphous silicon (a‐Si:H) p–i–n solar cells is carried out. The influence of the interface root‐mean‐square roughness and the effect of different angular distribution functions of diffused light on quantum efficiency and short‐circuit current are investigated by the optical model. Copyright © 2002 John Wiley & Sons, Ltd.     

Functionally Graded AA7075 Components Produced via Hot Stamping: A Novel Process Design Inspired from Analysis of Microstructure and Mechanical Properties

Herein, functionally graded AA7075 components manufactured via hot stamping are investigated by focusing on the effect of different process variables on localized microstructure evolution. To realize gradation through stamping, an active tool is designed and applied. The design of experiments allows to assess the impact of transfer time from the furnace to the tool, quenching time in the tool, and final quenching media. Related characteristics of mechanical properties throughout the hat-shaped profile are assessed via hardness and tensile tests. As expected, the sections of the samples formed in the cooled part of the tool are characterized by higher mechanical strength following subsequent aging, while sections formed in the heated part exhibit higher ductility. Moreover, the microstructural analysis reveals that fine precipitates with minimum interparticle distances only form in the cooled section of the samples. Increasing the tool temperature at the heated side to 350 °C results in the formation of coarse precipitates in the grain interior and along the grain boundaries. A sharp gradient in terms of microstructural and mechanical properties is found between these conditions. After reducing the transfer time, an increased volume fraction of fine precipitates leads to further improvements in hardness and mechanical strengths.     

Low-Cycle-Fatigue Performance of Stress-Aged EN AW-7075 Alloy

The effect of a novel heat treatment, that is, aging under superimposed external stress, on the fatigue performance and microstructural evolution of a high-strength aluminum alloy (EN AW-7075) is presented. Stress aging, a combination of heat treatment and superimposed external stress, can enhance the mechanical properties of EN AW-7075 under monotonic loading due to the acceleration of precipitation kinetics. Scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM) reveal that a longer aging time and the presence of superimposed stress both promote the formation and growth of precipitates, that is, the precipitation of strengthening η´ precipitates. This is confirmed by differential scanning calorimetry (DSC) heating experiments of stressless and stress-aged states. Furthermore, stress aging leads to a reduction of dimensions of precipitate-free zones near grain boundaries. Cyclic deformation responses (CDRs) and half-life hysteresis loops are evaluated focusing on the low-cycle fatigue (LCF) performance of different conditions. A noticeable cyclic hardening seen in case of the specimens aged for a short time indicates the occurrence of dynamic strain aging (DSA). Eventually, stress aging allows for an enhancement of the monotonic mechanical properties of EN AW-7075 without degrading the cyclic performance in the LCF regime.     

Repurposing of 8-Hydroxyquinoline-Based Butyrylcholinesterase and Cathepsin B Ligands as Potent Nonpeptidic Deoxyribonuclease I Inhibitors

A library of 31 butyrylcholinesterase (BChE) and cathepsin B (CatB) inhibitors was screened in vitro for inhibition of deoxyribonuclease I (DNase I). Compounds 22 , 8 and 7 are among the most potent synthetic non-peptide DNase I inhibitors reported to date. Three 8-hydroxyquinoline analogues inhibited both DNase I and BChE with IC₅₀ values below 35 μM and 50 nM, respectively, while two nitroxoline derivatives inhibited DNase I and Cat B endopeptidase activity with IC₅₀ values below 60 and 20 μM. Selected derivatives were screened for various co-target binding affinities at dopamine D₂ and D₃, histamine H₃ and H₄ receptors and inhibition of 5-lipoxygenase. Compound 8 bound to the H₃ receptor and is highlighted as the most promising multifunctional ligand with a favorable pharmacokinetic profile and one of the most potent non-peptide DNase I inhibitors. The present study demonstrates that 8-hydroxyquinoline is a structural fragment critical for DNase I inhibition in the presented series of compounds.