Dipolar magnetic order in the rare earth ethyl sulfates

The magnetic ground states of the ethyl sulfates of Nd, Gd, Ho, and Er have been determined by dc susceptibility measurements and found to agree with those predicted using (where possible) the classical Luttinger-Tisza theory. Ytterbium ethyl sulfate is not observed to order at temperatures above 6.5 mK. The observed transition temperatures scale roughly with the magnitude of the calculated ground state energy. The low-temperature paramagnetic susceptibility of Gd ethyl sulfate agrees qualitatively with a theoretical prediction based on experimental crystal-field parameters.     

E-4695, a new C-7 azetidinyl fluoronaphthyridine with enhanced activity against gram-positive and anaerobic pathogens

E-4695, (-)-7-[3-(R)-amino-2-(S)-methyl-1-azetidinyl]-1-cyclopropyl-1,4- dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid, is a new fluorinated naphthyridine with an azetidine moiety. The MICs of E-4695 at which 90% of the isolates were inhibited (MIC90s) were 0.06 to 0.5 microgram/ml for gram-positive cocci, including species of the genera Staphylococcus, Streptococcus, and Enterococcus, and the MIC90s against gram-negative pathogens such as members of the family Enterobacteriaceae (with the exception of Providencia spp. [MIC90, 8 micrograms/ml]) and Pseudomonas aeruginosa were 0.015 to 0.5 microgram/ml. E-4695 inhibited 90% of the Clostridium perfringens and Bacteroides fragilis isolates at 0.25 and 4 micrograms/ml, respectively. Against gram-positive cocci the potency of E-4695 was 2- to 8-fold higher than that of ciprofloxacin, 4- to 8-fold higher than that of ofloxacin, and 8- to 16-fold higher than that of fleroxacin. Against enteric bacteria and P. aeruginosa the potency of E-4695 was, in general, similar to that of ciprofloxacin and eightfold higher than those of ofloxacin and fleroxacin. E-4695 was four- and eightfold more potent than ciprofloxacin against C. perfringens and B. fragilis isolates, respectively. E-4695 and ciprofloxacin showed similar properties when the effects of pH or magnesium concentration were tested on them. E-4695 and ciprofloxacin had substantial reductions of activity only when pH decreased below 4.8. E-4695 and ciprofloxacin activities were not markedly affected by the presence of 5 or 10 mM Mg2+. The presence of serum and human urine at pH 7.2 decreased the activity of E-4695 between two- and fourfold. After an oral dose of 50 mg/kg of body weight, the maximum level in serum, the biological half-life, and the area under the concentration-time curve from 0 to 10 h for E-4695 were 13.2 microgram/ml, 3.3 h, and 45.6 microgram . h/ml, respectively. The area under the concentration-time curve from 0 to 4 h for ciprofloxacin was 2.3 microgram . h/ml at the same dose. Fifty-percent effective doses (ED50S) against Staphylococcus aureus HS-93 infections in mice were 4.5 mg/kg with E-4695 and 37.6 mg/kg with ciprofloxacin. Infection with Streptococcus pneumoniae 29206 was more effectively treated with E-4695 (ED50, 41,2 mg/kg) than with ciprofloxacin (ED50, 200 mg/kg). The ED50 of E-4695 for infections with Streptococcus pneumoniae 1625 was 132.2 mg/kg; ciprofloxacin was ineffective at 400 mg/kg against this strain. E-4695 was also more potent than ciprofloxacin in treatment of infections caused by gram-negative organisms such as Escherichia coli HM-42 (ED50S, 1.0 and 3.9 mg/kg, respectively). The ED50S of E-4695 and ciprofloxacin were 33.0 and 145.5 mg/kg against P. aeruginosa HS-116 and 9.6 and 18.9 mg/kg against P. aeruginosa B-120, respectively. The therapeutic efficacy of E-4695 may depend not only on its in vitro activity but also on its improved pharmacokinetic properties.     

Sol–gel immobilized aryl iodides for the catalytic oxidative α-tosyloxylation of ketones

New hybrid silica materials M1–M4, derived from mono and bis-silylated aryl iodides, have been prepared via sol–gel processes, either by the hydrolytic polycondensation of a bis-silylated monomer or by the co-gelification of a monosilylated precursor with tetraethylorthosilicate. They have been fully characterized by elemental analysis, ¹³C and ²⁹Si CP-MAS solid state NMR, IR, TGA, and nitrogen-sorption measurements. These organosilicas have been successfully applied as supported catalysts in the α-tosyloxylation of aliphatic ketones in the presence of m-chloroperbenzoic acid (m-CPBA) as an oxidant, with the corresponding α-tosyloxyketones obtained in moderate to good isolated yields. The recyclability of the supported catalysts by a simple filtration has also been investigated.     

Structured latex particles with improved mechanical properties

Structured polymer latex particles are prepared by a swelling emulsion polymerization process, in which the initial particles are first swollen by ethylenically unsaturated monomers and the polymerization of the latter is then carried out. This special polymerization process leads to multi-phase particle morphology. Instead of a thermodynamically more favorable large-scale phase-separation, we obtain multiple, near-spherical domains dispersed within the particles. TEM analysis after selective staining reveals the size and distribution of the microdomains. Dynamic mechanical analysis of the polymer films confirms the absence of a distinct, large second phase and indicates that such microdomains interfere at the molecular level with the segmental mobility of the dispersing phase. We present examples of soft polymers as the continuous phase and hard polymers as the dispersed phase. The inclusion of hard microdomains into soft continuous phase increases dramatically both the films tensile strength and elongation, which means improved cohesive strength of the polymer material. The increase in tensile strength of the polymer film correlates directly with the hardness of the dispersed phase. Improvement in tensile strength and elongation is important in a number of industrial applications of polymers, such as flexible coatings, coalescent-free paints and pressure sensitive adhesives (PSAs). Examples are presented which demonstrate the potential applications of the swelling emulsion polymerization process.     

Recoverable Palladium Catalysts for Suzuki–Miyaura Cross‐ Coupling Reactions Based on Organic‐Inorganic Hybrid Silica Materials Containing Imidazolium and Dihydroimidazolium Salts

The systems formed by palladium acetate [Pd(OAc)₂] and hybrid silica materials prepared by sol‐gel from monosilylated imidazolium and disilylated dihydroimidazolium salts show catalytic activity in Suzuki–Miyaura cross‐couplings with challenging aryl bromides and chlorides. They are very efficient as recoverable catalysts with aryl bromides. Recycling is also possible with aryl chlorides, although with lower conversions. In situ formation of palladium nanoparticles has been observed in recycling experiments.     

The use of caffeine to assess high dose exposures to ionising radiation by dicentric analysis

Dicentric analysis is considered as a 'gold standard' method for biological dosimetry. However, due to the radiation-induced mitotic delay or inability to reach mitosis of heavily damaged cells, the analysis of dicentrics is restricted to doses up to 4-5 Gy. For higher doses, the analysis by premature chromosome condensation technique has been proposed. Here, it is presented a preliminary study is presented in which an alternative method to analyse dicentrics after high dose exposures to ionising radiation (IR) is evaluated. The method is based on the effect of caffeine in preventing the G2/M checkpoint allowing damaged cells to reach mitosis. The results obtained indicate that the co-treatment with Colcemid and caffeine increases significantly increases the mitotic index, and hence allows a more feasible analysis of dicentrics. Moreover in the dose range analysed, from 0 to 15 Gy, the dicentric cell distribution followed the Poisson distribution, and a simulated partial-body exposure has been clearly detected. Overall, the results presented here suggest that caffeine has a great potential to be used for dose-assessment after high dose exposure to IR.     

Demonstration of spectral and spatial interferometry at THz frequencies

A laboratory prototype spectral-spatial interferometer has been constructed to demonstrate the feasibility of the double-Fourier technique at far infrared (FIR) wavelengths (0.15-1 THz). It is planned to use this demonstrator to investigate and validate important design features and data-processing methods for future astronomical FIR interferometer instruments. In building this prototype, we have had to address several key technologies to provide an end-end system demonstration of this double-Fourier interferometer. We report on the first results taken when viewing single-slit and double-slit sources at the focus of a large collimator used to simulate real sources at infinity. The performance of the prototype instrument for these specific field geometries is analyzed to compare with the observed interferometric fringes and to demonstrate image reconstruction capabilities.