Triblock and Radial Star-Block Copolymers Comprised of Poly(ethoxyethyl glycidyl ether), Polyglycidol,Poly(propylene oxide) and Polystyrene Obtained by Anionic Polymerization Initiated by Cs Initiators

The anionic polymerization of ethoxyethyl glycidyl ether (EEGE) initiated by cesium alkoxide was studied. The ring-opening polymerization of EEGE in the presence of cesium alkoxide of 1-methoxy-2-ethanol does not involve any side reactions. The presence of an additional alcohol leads to a significant increase of the initiator efficiency. Aqueous solutions of poly (ethoxyethyl glycidyl ether) (PEEGE) exhibit lower critical solution temperature (LCST), and the polymer solubility in water is extremely sensitive to its MW. Two novel types of block copolymers based on PEEGE were synthesized: triblock-copolymers of ABA (A′:BA′) structure, where A is the PEEGE block, A′ polyglycidol (PG) and B the polypropylene oxide (PPO) block, and A₂S (A′₂S) and A₄S (A′₄S) heteroarm stars, where S is the polystyrene block. The synthesis of the ABA block was performed by polymerization of EEGE initiated by bi-functional PPO/Cesium alkoxide macroinitiator. The PEEGE blocks were converted into PG blocks by successful cleavage of the ethoxyethyl group. Polystyrene/PEEGE and polystyrene/PG three- and five- heteroarm star copolymers were synthesized by a coupling reaction between well-defined chain-end-functionalized polystyrenes carying dendritic benzyl bromide moieties with living anionic polymers of PEEGE with one cesium alkoxide terminal group. The coupling reaction proceeds quantitatively without any side reactions, and thus series of star-branched polymers can be systematically synthesized. Polystyrenes with two or four PG arms have been obtained after the cleavage of the protecting group. The compact structure of these multi-arm star polymers and their amphiphilic character leads to the formation of nanoparticles in aqueous solution with rather uniform size distribution and a mean diameter of 15 nm.     

Development and validation of a liquid chromatographic method for the analysis of positron emission tomography radiopharmaceuticals with Ru(bpy)(3)(2+)-KMnO(4) chemiluminescence detection.

A sensitive, selective and rapid high-performance liquid chromatographic (HPLC) method with chemiluminescence (CL) detection was developed and validated for the analysis of positron emission tomography (PET) radiopharmaceuticals. This method is based on the CL reaction of PET compounds with tris(2,2'-bipyridyl)ruthenium(II) [Ru(bpy)(3)(2+)] and acidic potassium permanganate [KMnO(4)]. After optimization of the reaction conditions, 12 of the 14 PET compounds investigated could be successfully detected and showed good performance in terms of sensitivity, linearity and reproducibility. In particular, for compounds with a tertiary amine functional group, the limits of detection were ppb levels for a 20 microL injection volume. Finally, this method was used to determine PET compounds for calculating of specific radioactivity in pharmaceutical samples.     

An in-syringe La-coprecipitation Method for the Preconcentration of Oxo-anion Forming Elements in Seawater Prior to an ICP-MS Measurement

A lanthanum (La) coprecipitation method with low sample consumption was explored for the preconcentration of oxo-anion forming elements prior to a measurement by inductively coupled plasma mass spectrometry (ICP-MS). The preconcentration procedure was composed of two main steps: (1) the formation of a coprecipitate with the lowest possible La and (2) the redissolution of target analytes with minimal use of nitric acid, and the elimination of high concentration La from the analysis sample. Each step was performed in a 25 mL-volume syringe to reduce the sample consumption and to avoid contamination from the experimental environment. Various parameters, such as the concentration and volume of La added into the sample solution, the precipitation pH, the aging time, and the volume of HNO(3) were optimized to obtain good recoveries and high detection sensitivities for V, As, Sb, and W, which could be hardly recovered by solid-phase extraction using a chelating resin. The obtained method was evaluated through the analysis of seawater reference materials (CASS-4 and NASS-5). The recoveries exceeded 80%, and the observed values were in good agreement with the certified values.     

Time-series analysis of sleep-wake stage of rat EEG using time-dependent pattern entropy

We performed electroencephalography (EEG) for six male Wistar rats to clarify temporal behaviors at different levels of consciousness. Levels were identified both by conventional sleep analysis methods and by our novel entropy method. In our method, time-dependent pattern entropy is introduced, by which EEG is reduced to binary symbolic dynamics and the pattern of symbols in a sliding temporal window is considered. A high correlation was obtained between level of consciousness as measured by the conventional method and mean entropy in our entropy method. Mean entropy was maximal while awake (stage W) and decreased as sleep deepened. These results suggest that time-dependent pattern entropy may offer a promising method for future sleep research.     

Chemical states of dodecanethiolate-passivated Au nanoparticles: synchrotron-radiation photoelectron spectroscopy

We have carried out a photoemission study using synchrotron radiation of dodecanethiolate (DT)-passivated Au nanoparticles supported on the highly oriented pyrolytic graphite substrates. From detailed line-shape analyses of Au 4f core-level photoemission spectra of DT-passivated Au nanoparticles, it was found that Au 4f core-level spectra consist of two components. We attribute these components to the inner Au atoms and surface Au atoms bonded to surface dodecanethiolates. From these results, we discuss the chemical states of the present DT-passivated Au nanoparticles.     

Electric Field Enhancement of Nano Gap of Silver Prisms

Using numerical calculation, we examine the effects of gap distance of a pair of nano gap silver prisms with rounded corners on the local light intensity enhancement. Two peaks due to localized surface plasmon （LSP） excitation are observed in a wavelength range from 900nm to 300nm. The results demonstrate that peaks at a longer and a shorter wavelength corresponded to dipole-like and quadrupole-like LSP resonances, respectively. It is found that a gap distance up to 20 nm provides larger light intensity enhancement than that of a single silver nano prism with rounded corners. Furthermore, nano gap silver prisms are fabricated by direct focused ion beam processing, and we measure the scattering light spectrum of a pair of nano prisms by a confocal optical system. However, the two LSP peaks are not observed in visible range because the sizes of the nano gap and prisms are too large.     

Characterization of boron carbon nitride film modified by excimer laser annealing

Boron carbon nitride (BCN) shows promise as a field emitter material because of its mechanical hardness, chemical inertness, and low electron affinity. This study investigated the modification of a BCN film with an amorphous area using KrF excimer laser (wavelength: 248 nm, photon energy: 5.0 eV) annealing without substrate heating. This achieved significant variation in characteristics, such as an increase in bandgap energy and decrease in electron affinity. Laser annealing reduced electron affinity from 0.7 to 0.3 eV. The results indicate that the modification of the BCN film by KrF excimer laser annealing achieves characteristics similar to hexagonal BN (h-BN) film without losing the desirable properties of the BCN film, such as physical stability.     

Application of an atmospheric pressure helium microwave-induced plasma as an element-selective detector for gas chromatography

An atmospheric pressure helium microwave-induced plasma (MIP) was combined with a gas chromatograph (GC). and used as an element-selective detector for GC. The detection limits, dynamic ranges and selectivities were obtained for H, C, F, Cl, Br, I and S. Such data for nitrogen and oxygen could not be obtained because of the interference from air which was entrained into the system through the leakages of the tubing and the valve system. The detection limits and dynamic ranges for all the elements investigated were in a range between 1.8 and 39pgs^?1 and between 1.6 × 10³ and 1.1 × 10⁵, respectively. Furthermore, the relative sensitivities of C, H, Cl and Br for various compounds were examined. In the cases of carbon and hydrogen, the relative sensitivities were not the same for different compounds containing oxygen and nitrogen. This result may be explained by the incomplete decomposition of such compounds due to the low microwave power (75 W) applied in the present system.