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1.
The states of 104Pd, populated in the EC-β+ decay of the ground ( J π = 5+) and metastable ( J π = 2+) states of 104Ag, have been investigated in the framework of the proton-neutron interacting boson model, extending a previous analysis to take into account the newly appeared experimental data. All positive-parity states up to an excitation energy of 3 MeV and spin in the range J = 1-6, fed by more than 0.3% in the decay of the parent nucleus, have been considered. As a result, strong evidence has been found for interpreting most of these states as states of collective nature having a quite pure full- or mixed-symmetry character and, in particular, for identifying the 1+ level at 2276 keV as the lowest 1+ mixed-symmetry state.  相似文献   
2.
We report herein studies on the liquid crystalline behavior of a series of supramolecular materials that contain different ratios of two complementary symmetrically-substituted alkoxy-bis(phenylethynyl)benzene AA- and BB-type monomers. One monomer has thymine units placed at either end of the rigid mesogenic core, while the other has N6-(4-methoxybenzoyl)-adenine units placed on the ends. Differential scanning calorimetric and polarized optical microscopy studies have been carried out on these systems. These studies show that the material's behavior is strongly dependent on its thermal history. As a result, the materials can exhibit, on heating, either a liquid crystalline phase, a crystalline phase, or the coexistence of crystalline and liquid crystalline regions. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5049–5059, 2006  相似文献   
3.
Michael additions of a β,γ-unsaturated ester and a nitrile to a variety of α,β-unsaturated ketones can be effected with high regioselectivity and in good yields using P(i-PrNCH2CH2)3N as a catalyst.  相似文献   
4.
A procedure has been developed for the direct fourth-derivative spectrophotometric determination of iron(III) dimethyldithiocarbamate by converting it into an iron(II) 2,2'-bipyridyl complex, which is then dissolved in Triton X-100. Beer's law is obeyed over the concentration range 0.5-20 microg mL(-1 )in the final solution. Various parameters such as the effect of pH and interference of large number of ions on the determination of ferbam have been studied in detail. The method is sensitive, highly selective and can be used for the determination of ferbam in a commercial sample and in mixtures with various dithiocarbamates (ziram, zineb, maneb, etc.) and from wheat grains.  相似文献   
5.
Preparation and some reactions of the first cumulated ylide of arsenic, viz. triphenylarsoranylideneketene are described.  相似文献   
6.
Summary Hydrazine, an oxygen scavenger in boiler water, was derivatised to the corresponding acetone azine and determined at the ng ml–1 level by gas chromatography. Morpholine, a corrosion inhibitor used in steam boilers, was estimated either directly (if >2.0 g ml–1) or by quantitative preconcentration (0.1 ng – 2.0 g ml–1). To obtain symmetrical peaks for these amines, the column packing was coated with KOH. Use of a nitrogen-specific detector improved accuracy of estimation of hydrazine and morpholine, giving a RSD of 1.9–3.6%. Chromatographic analysis of these amines in boiler feed water and steam condensate samples collected from boilers servicing a petroleum refinery is described. Environmental safety regulations calls for monitoring of hydrazine and the methods developed can easily be adapted for this purpose.  相似文献   
7.
Measurements of the specific heat of two alloys of Ce (0.00275 and 0.0121 at % Ce) in Al have been made in the region 0.3<T<3.8 K. Within the limits of detection (<1 ppm), the alloys contained no metallic impurities other than Ce and their homogeneity was checked by neutron activation analysis. For the alloys in their normal electronic states, the change/c was found to be 6±3 and 3.5±1.5mJ/at% K2. The behavior of the alloys in their superconducting states (e.g.: the shift ofT c with the concentration of Ce; the correlation betweenT C/TC0 andC/C 0) indicates the existence of short-lived local moments associated with the Ce impurities.  相似文献   
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Novel drug delivery systems capable of continuous sustained release of therapeutics have been studied extensively for use in the prevention and management of chronic diseases. The use of these systems holds promise as a means to achieve higher patient compliance while improving therapeutic index and reducing systemic toxicity. In this work, an implantable nanochannel drug delivery system (nDS) is characterized and evaluated for the long-term sustained release of atorvastatin (ATS) and trans-resveratrol (t-RES), compounds with a proven role in managing atherogenic dyslipidemia and promoting cardioprotection. The primary mediators of drug release in the nDS are nanofluidic membranes with hundreds of thousands of nanochannels (up to 100,000/mm2) that attain zero-order release kinetics by exploiting nanoconfinement and molecule-to-surface interactions that dominate diffusive transport at the nanoscale. These membranes were characterized using gas flow analysis, acetone diffusion, and scanning and transmission electron microscopy (SEM, TEM). The surface properties of the dielectric materials lining the nanochannels, SiO2 and low-stress silicon nitride, were further investigated using surface charge analysis. Continuous, sustained in vitro release for both ATS and t-RES was established for durations exceeding 1 month. Finally, the influence of the membranes on cell viability was assessed using human microvascular endothelial cells. Morphology changes and adhesion to the surface were analyzed using SEM, while an MTT proliferation assay was used to determine the cell viability. The nanochannel delivery approach, here demonstrated in vitro, not only possesses all requirements for large-scale high-yield industrial fabrication, but also presents the key components for a rapid clinical translation as an implantable delivery system for the sustained administration of cardioprotectants.  相似文献   
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