Polarized organic electroluminescence: Ordering from the top

We demonstrate a method for achieving polarized organic electroluminescence for liquid crystalline conjugated polymers that allows the polymer to be deposited directly onto the anode. The technique utilizes a top-down alignment approach whereby the predeposited polymer was aligned from above using a rubbed polyimide master and a smectic liquid crystal transfer layer. The liquid crystal/polyimide master bilayer was sandwiched with the liquid crystalline polymer that had been deposited onto the electrode. The sandwiched layers were then heated to achieve alignment before the removal of the polyimide master and liquid crystal transfer layer. Using this method, poly[2,7-{9,9-di(2-ethylhexyl)}fluorene] (PF2-6) was aligned to give an anisotropic polymer film. Light emitted from single layer light-emitting diodes containing the aligned PF2-6 had integrated dichroic ratios of up to 9.7. At 100 cd/m(2), the single layer devices had external quantum and power efficiencies of 0.08% and 0.05 lm/W, respectively. Bilayer devices containing an electron transport layer between the PF2-6 and the cathode gave emitted light with good dichroic ratios and with the external quantum and power efficiencies at 100 cd/m(2) being increased to 2.2% and 1.1 lm/W. (C) 2003 American Institute of Physics

New Zinc-Based Active Chitosan Films: Physicochemical Characterization, Antioxidant, and Antimicrobial Properties

The improvement of the antioxidant and antimicrobial activities of chitosan (CS) films can be realized by incorporating transition metal complexes as active components. In this context, bioactive films were prepared by embedding a newly synthesized acylpyrazolonate Zn(II) complex, [Zn(QPhtBu)2(MeOH)2], into the eco-friendly biopolymer CS matrix. Homogeneous, amorphous, flexible, and transparent CS@Znn films were obtained through the solvent casting method in dilute acidic solution, using different weight ratios of the Zn(II) complex to CS and characterized by powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared (FT-IR), Raman, and scanning electron microscopy (SEM) techniques. The X-ray single-crystal analysis of [Zn(QPhtBu)2(MeOH)2] and the evaluation of its intermolecular interactions with a protonated glucosamine fragment through hydrogen bond propensity (HBP) calculations are reported. The effects of the different contents of the [Zn(QPhtBu)2(MeOH)2] complex on the CS biological proprieties have been evaluated, proving that the new CS@Znn films show an improved antioxidant activity, tested according to the DPPH method, with respect to pure CS, related to the concentration of the incorporated Zn(II) complex. Finally, the CS@Znn films were tried out as antimicrobial agents, showing an increase in antimicrobial activity against Gram-positive bacteria (Staphylococcus aureus) with respect to pure CS, when detected by the agar disk-diffusion method

Experiments on hot and dense laser-produced plasmas

Plasmas generated by irradiating targets with {approx}20 kJ of laser energy are routinely created in inertial confinement fusion research. X-ray spectroscopy provides one of the few methods for diagnosing the electron temperature and electron density. For example, electron densities approaching 10{sup 24} cm{sup -3} have been diagnosed by spectral linewidths. However, the accuracy of the spectroscopic diagnostics depends on the population kinetics, the radiative transfer, and the line shape calculations. Analysis for the complex line transitions has recently been improved and accelerated by the use of a database where detailed calculations can be accessed rapidly and interactively. Examples of data from Xe and Ar doped targets demonstrate the current analytic methods. First we will illustrate complications that arise from the presence of a multitude of underlying spectral lines. Then, we will consider the Ar He-like 1s{sup 2}({sup 1}S{sub 0}) - 1s3p({sup 1}P{sub 0}) transition where ion dynamic effects may affect the profile. Here, the plasma conditions are such that the static ion microfield approximation is no longer valid; therefore in addition to the width, the details of the line shape can be used to provide additional information. We will compare the data to simulations and discuss the possible pitfalls involved in demonstrating the effect of ion dynamics on lineshapes

The anti-bacterial iron-restriction defence mechanisms of egg white; the potential role of three lipocalin-like proteins in resistance against Salmonella

Salmonella enterica serovar Enteritidis (SE) is the most frequently-detected Salmonella in foodborne outbreaks in the European Union. Among such outbreaks, egg and egg products were identified as the most common vehicles of infection. Possibly, the major antibacterial property of egg white is iron restriction, which results from the presence of the iron-binding protein, ovotransferrin. To circumvent iron restriction, SE synthesise catecholate siderophores (i.e. enterobactin and salmochelin) that can chelate iron from host iron-binding proteins. Here, we highlight the role of lipocalin-like proteins found in egg white that could enhance egg-white iron restriction through sequestration of certain siderophores, including enterobactin. Indeed, it is now apparent that the egg-white lipocalin, Ex-FABP, can inhibit bacterial growth via its siderophore-binding capacity in vitro. However, it remains unclear whether ex-FABP performs such a function in egg white or during bird infection. Regarding the two other lipocalins of egg white (Cal-γ and α-1-glycoprotein), there is currently no evidence to indicate that they sequester siderophores

New pi-electron rich donors and cavities and their supramolecular assemblies: Synthesis, electrochemistry and crystal structures

The synthesis, solution redox properties and X-ray crystal structures of 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives are described

Molecular saddles. 4. Redox-active cyclophanes by bridging the 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene system: Synthesis, electrochemistry, and X-ray crystal structures of neutral species and a dication salt

We report the synthesis of a new series of cyclophanes 11a-d by ester-forming macrocyclization reactions of diol 9 with the dicarbonyl chloride derivatives of benzene, thiophene, ferrocene, and diphenyl ether, 10a-d, respectively. Compounds 11a-d display a two-electron, quasireversible oxidation wave in the cyclic voltammogram to yield the dication species at E- pa(ox) = 0.70-0.72 V (for 11a-c) and 0.47 V (for 11d) (vs Ag/AgCl in acetonitrile). The raised oxidation potentials for 11a-c reflect the reduced stability of the twisted dication structure within the steric constraints of the smaller cyclophanes. Consistent with this, the value of DeltaE (defined as E-pa(ox) - E-pc(ox)) decreases (i.e., reversibility of the oxidation process increases) in the sequence 11d > 11c > 11a > 11b as the bridging chain becomes shorter. X-ray crystal structures are reported for compounds 11a-d and the dication salt 11d(2+)(I-3(-))(2). (CH2Cl2)(2.25). For 11a-d the typical saddle-shaped conformation of the 9,10-bis( 1,3-dithiol-2- ylidene)-9, 10-dihydroanthracene moiety is observed, with the strain imposed by the cyclophane ring being accommodated in the structure of the bridging unit. In the dication 11d(2+) both dithiolium rings are planar and the anthracene unit is essentially aromatic, with the conformation of the bridge basically the same as in neutral 11d