Compositionally graded interface for passivation of HgCdTe photodiodes

A compositionally graded CdTe-Hg_1−xCd_xTe interface was created by deposition of CdTe on p-HgCdTe and subsequent annealing. The compositionally graded layer between CdTe and HgCdTe was formed by an interdiffusion process and was used for passivation. The composition gradient (Δx) in the interfacial region and the width of the graded region were tailored by adopting a suitable annealing procedure. The effect of process conditions on the interfacial profile and photoelectric properties such as lifetime and surface recombination velocity was studied in detail. Surface recombination velocity of the p-HgCdTe could be reduced to the level of 3,000 cm/s at 77 K, which represents very good passivation characteristics. The passivation layer formed by this method can be used for the fabrication of high performance and stable modern infrared detectors. Thus, a passivation process is developed, which is simple, effective, reproducible, and compatible with the HgCdTe device fabrication and packaging processes.     

The inclusive reactions π+d → π− + anything and π+d → π−π− + anything at 6 and 24 GeV/c

Inclusive production of π^? mesons has been studied with 6 and 24 GeV/cπ⁺ beams interacting in deuterium bubble chambers. The energy dependence of the inclusive spectra is discussed. In comparisons with π⁺p inclusive interactions, we observe that projectile fragmentation is not independent of the nature of the target at 6 GeV/c. Cross sections and ratios of cross sections are presented. Two-particle correlations are found to be similar at both energies.     

Determination of small phosphorus-containing compounds by capillary electrophoresis

The review focuses on the analysis of small phosphorus-containing compounds by capillary electrophoresis (CE) with different detection modes including UV absorption, laser-induced fluorescence, conductometry, amperometry, atomic spectrometry, and mass spectrometry. Determinations of phosphates, organophosphate, and chemical warfare agents in environmental samples such as water, soil and grains are emphasized. To achieve better sensitivity, high-resolving power, and reproducibility, the optimum separation conditions for various analytes (samples) are different. We compare the merits and demerits of the different detection modes for the detection of the analytes. Although the present methods are successful in many cases, there is still a need to develop high-throughput CE techniques for screening numerous environmental samples and sample stacking techniques in CE for the analysis of trace analytes.     

Spectrophotometric determination of mebeverine hydrochloride

Three simple, sensitive and reproducible visible spectrophotometric methods (A-C) for the determination of mebeverine hydrochloride (MVH) in bulk samples and pharmaceutical formulations are described. Methods A and B are based on the formation of ion-association complexes between the drug and fast green FCF (FGFCF, _max 625 nm) or bromothymol blue (BTB, _max 405 nm). Method C is based on the formation of a molecular complex between the drug and cobalt thiocyanate (CTC, _max 625 nm). Regression analysis of Beer's plots showed good correlation in the concentration ranges 2–40, 2–25 and 100–600 g/ml for methods A, B and C respectively. No interference was observed from the usually existing additives in pharmaceutical formulations and the applicability of the methods was examined by analysing tablets containing MVH. Standard deviations were typically 0.75 mg per dose (RSD: 0.25–0.5%). Recoveries were 99.0–100.2%.     

Three-component coupling reactions in ionic liquids: One-pot synthesis of isoxazolidines

1-Butyl-3-methylimidazolium based ionic liquids are found to accelerate significantly the intermolecular 1,3-dipolar cycloaddition of nitrones derived in situ from aldehydes and phenyl hydroxylamine, with electron deficient olefins to afford enhanced rates and improved yields of isoxazolidines with high regio- and diastereoselectivity.     

Synthesis and antimicrobial activity of some new N‐(substituted phenyl)‐N′‐[2,3‐dihydro‐2‐oxido‐3‐(4′‐fluorophenyl)‐1H‐(1,3,2)benzoxazaphosphorin 2‐yl]ureas

Substituted benzoxazaphosphorin 2‐yl ureas were synthesized by reacting 2‐(4‐fluoro‐phenylamino)‐methylphenol (4) with different carbamidophosphoric acid dichlorides (3) in the presence of triethylamine in dry toluene at 45‐50 °C and characterized by spectral data. These compounds were found to possess good antimicrobial activity.     

Dramatic influence of the orientation of linker between hydrophilic and hydrophobic lipid moiety in liposomal gene delivery

A number of prior studies have demonstrated that the DNA-binding and gene transfection efficacies of cationic amphiphiles crucially depend on their various structural parameters including hydrophobic chain lengths, headgroup functionalities, and the nature of the linker-functionality used in tethering the polar headgroup and hydrophobic tails. However, to date addressing the issue of linker orientation remains unexplored in liposomal gene delivery. Toward probing the influence of linker orientation in cationic lipid mediated gene delivery, we have designed and synthesized two structurally isomeric remarkably similar cationic amphiphiles 1 and 2 bearing the same hydrophobic tails and the same polar headgroups connected by the same ester linker group. The only structural difference between the cationic amphiphiles 1 and 2 is the orientation of their linker ester functionality. While lipid 1 showed high gene transfer efficacies in multiple cultured animal cells, lipid 2 was essentially transfection incompetent. Findings in both transmission electron microscopic and dynamic laser light scattering studies revealed no significant size difference between the lipoplexes of lipids 1 and 2. Findings in confocal microscopic and fluorescence resonance energy transfer (FRET) experiments, taken together, support the notion that the remarkably higher gene transfer efficacies of lipid 1 compared to those of lipid 2 presumably originate from higher biomembrane fusogenicity of lipid 1 liposomes. Differential scanning calorimetry (DSC) and fluorescence anisotropy studies revealed a significantly higher gel-to-liquid crystalline temperature for the lipid 2 liposomes than that for lipid 1 liposomes. Findings in the dye entrapment experiment were also consistent with the higher rigidity of lipid 2/cholesterol (1:1 mole ratio) liposomes. Thus, the higher biomembrane fusibility of lipid 1 liposomes than that of lipid 2 liposomes presumably originates from the more rigid nature of lipid 2 cationic liposomes. Taken together, the present findings demonstrate for the first time that even as minor a structural variation as linker orientation reversal in cationic amphiphiles can profoundly influence DNA-binding characteristics, membrane rigidity, membrane fusibility, cellular uptake, and consequently gene delivery efficacies of cationic liposomes.     

Cycloaddition of bis‐1,3‐dipolar reagents to 1,3‐diarylprop‐2‐en‐1‐ones

Bis pyrazolines and isoxazolines were prepared by 1,3‐dipolar cycloaddition of benzene‐1,3/1,4‐dicarboxaldehyde dihydrazones and dioximes to 1,3‐diaryl‐prop‐2‐en‐1‐ones. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:379–383, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10169     

Large eddy simulation of temporally developing juncture flows

Large eddy simulation (LES) results are reported for temporally developing solid–solid and solid–rigid-lid juncture flows. A MacCormack-type scheme that is second-order in time, and fourth-order in space for the convective terms and second-order in space for the viscous terms, is used. The simulations are obtained for a low subsonic Mach number. The subgrid-scale stresses (SGS) are modeled using the dynamic modeling procedure. The turbulent flow field generated on a flat-plate boundary layer is used to initialize the juncture flow simulations. The results of the flat-plate boundary layer simulations are validated with experimental and direct numerical simulations (DNS) data. In juncture flow simulations, the presence of an adjacent solid-wall/rigid-lid boundary altered the mean and the turbulent field, setting up gradients in the anisotropy of normal Reynolds stresses resulting in the formation of turbulence-induced secondary vortices. The relative size of these secondary vortices and the distribution of mean and turbulent quantities are in qualitative agreement with the experimental observations for the solid–solid juncture. The overall distribution of the mean and turbulence quantities showed close resemblance between the solid–solid and the solid–rigid-lid junctures; except for the absence of a second vortical region near the rigid-lid boundary. In agreement with the experimental observations, it was found that the normalized anisotropy term exhibited similarity when plotted against the distance from the boundary, regardless of the type of boundary, i.e. solid-wall or rigid-lid. The turbulent kinetic energy increased near the rigid-lid boundary. While the surface normal velocity fluctuations decreased to zero at the rigid-lid boundary, the other two velocity components showed an increase in their energy, which is also consistent with the experimental observations. © 1998 John Wiley & Sons, Ltd.     

Novel Indole‐Quinazolinone Based Amides as Cytotoxic Agents

Indole‐quinazolinone hybrids with active amides were synthesized, characterized, and assessed for their cytotoxicity. Two molecules displayed substantial activity in sulphorhodamine B assay method.