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F. Herfurth K. Blaum S. Eliseev O. Kester H.-J. Kluge S. Koszudowski C. Kozhuharov G. Maero D. Neidherr W. Quint S. Schwarz S. Stahl G. Vorobjev 《Hyperfine Interactions》2006,173(1-3):93-101
A decelerator will be installed at GSI in order to provide and study heavy nuclei without or with only few electrons at very
low energies or even at rest. Highly-charged ions will be produced by stripping at relativistic energies. After electron cooling
and deceleration in the Experimental Storage Ring (ESR) the ions are ejected out of the storage ring at 4 MeV/u and further
decelerated in a combination of linear accelerator structures operated in reverse. Finally, they are injected into a Penning
trap where the ions are cooled to 4 K by electron cooling in combination with resistive cooling. From here, the ions can be
transferred in a quasi DC or in a pulsed mode to different experimental setups. This article describes the technical concepts
of this project focused on the Penning trap.
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We investigate which types of asymptotic distributions can be generated by the knots of convergent sequences of interpolatory integration rules. It will turn out that the class of all possible distributions can be described exactly, and it will be shown that the zeros of polynomials that are orthogonal with respect to varying weight functions are good candidates for knots of integration rules with a prescribed asymptotic distribution.Research supported by the Deutsche Forschungsgemeinschaft (AZ: Sta 299/4-2). 相似文献
5.
Herbert Stahl 《Constructive Approximation》1989,5(1):221-240
Letf be an analytic function with all its singularities in a compact set \(E_f \subset \bar C\) of (logarithmic) capacity zero. The function may have branch points. The convergence of generalized (multipoint) Padé approximants to this type of function is investigated. For appropriately selected schemes of interpolation points, it is shown that close-to-diagonal sequences of generalized Padé approximants converge in capacity tof in a certain domain that can be characterized by the property of the minimal condenser capacity. Using a pole elimination procedure, another set of rational approximants tof is derived from the considered generalized Padé approximants. These new approximants converge uniformly on a given continuum \(V \subset \bar C\backslash E_f\) with a rate of convergence that has been conjectured to be best possible. The continuumV is assumed not to divide the complex plane. 相似文献
6.
The Pd(OAc)2/O2/DMSO catalyst system displays impressive versatility in the aerobic oxidation of organic substrates, ranging from alcohols to olefins. This report details mechanistic insights into these reactions. Dimethyl sulfoxide (DMSO) plays no redox role in the chemistry, and kinetic experiments identify the turnover-limiting step as DMSO-promoted oxidation of palladium(0) by molecular oxygen. The "chemical oxidase" pathway characterized for this catalyst system holds great promise for the design of new aerobic oxidation reactions. 相似文献
7.
Losses of H2 and H2O from the [M-H]? alkoxide anions of 1,4-cyclohexanediol formed in OH? negative chemical ionization were studied using synthetic deuterated analogues and labelling by hydrogen-deuterium exchange between neutrals in the ion source prior to ionization. Simple 1,2-H2 elimination leading to an enolate ion does not occur, but stereospecific mechanisms are shown to give a ketolate intermediate daughter ion. Collisionally activated dissociation spectra of the resulting daughter ions are the same as those of the corresponding ions generated directly from ketols. 相似文献
8.
G. Allan Stahl 《Journal of polymer science. Part A, Polymer chemistry》1981,19(2):371-380
The relative reactivity of acrylic acid is known to be influenced by the polymerization medium. Nonetheless, the more commonly used reactivity ratios do not show this dependence because they were calculated from low-conversion polymerizations. We have studied the copolymerization of acrylic acid and methyl methacrylate in a number of non-hydrogen-bonding and hydrogen-bonding solvents. We found that the acrylic acid fraction in the copolymer was larger when copolymerized in a non-hydrogen-bonding medium and that the methyl methacrylate fraction was larger when copolymerized in a hydrogen-bonding medium. The precise reactivity ratios were reported when toluene, benzene, isopentyl, acetate, ethyl acetate, methyl formate, and tert-butyl alcohol were used as the polymerization medium. The values were obtained by chromatographic analysis of residual monomer, followed by computation based on the nonlinear, least-squares technique of Tidwell and Mortimer. 相似文献
9.
Pressure-supported packed capillary electrochromatography (CEC) and packed capillary high-performance liquid chromatography (pHPLC) have been coupled on-line to electrospray ionization-mass spectrometry (ESI-MS) and coordination ion spray-mass spectrometry (CIS-MS). Separation of enantiomers of barbiturates and chlorinated alkyl phenoxypropanoates were performed on a permethylated beta-cyclodextrin stationary phase by pressure-supported CEC. For on-line detection with ESI- and CIS-MS, a modified sheath-liquid interface was used. CIS-MS is a universal, novel ionization technique which improves the selectivity as well as the sensitivity. Charged complexes were formed through the addition of central complexing ions such as silver(I), cobalt(II), copper(II), and lithium(I) to the sheath flow. Advantages of CIS-MS detection compared to the ESI-MS mode are discussed. In the CIS-MS mode, increased sensitivity and high selectivity was attained through different possibilities of complexation. The superiority of pressure-supported CEC compared to pHPLC in the hyphenation with CIS-MS is demonstrated. 相似文献
10.
The Pd(OAc)(2)/pyridine catalyst system is one of the most convenient and versatile catalyst systems for selective aerobic oxidation of organic substrates. This report describes the catalytic mechanism of Pd(OAc)(2)/pyridine-mediated oxidation of benzyl alcohol, which has been studied by gas-uptake kinetic methods and (1)H NMR spectroscopy. The data reveal that turnover-limiting substrate oxidation by palladium(II) proceeds by a four-step pathway involving (1) formation of an adduct between the alcohol substrate and the square-planar palladium(II) complex, (2) proton-coupled ligand substitution to generate a palladium-alkoxide species, (3) reversible dissociation of pyridine from palladium(II) to create a three-coordinate intermediate, and (4) irreversible beta-hydride elimination to produce benzaldehyde. The catalyst resting state, characterized by (1)H NMR spectroscopy, consists of an equilibrium mixture of (py)(2)Pd(OAc)(2), 1, and the alcohol adduct of this complex, 1xRCH(2)OH. These in situ spectroscopic data provide direct support for the mechanism proposed from kinetic studies. The catalyst displays higher turnover frequency at lower catalyst loading, as revealed by a nonlinear dependence of the rate on [catalyst]. This phenomenon arises from a competition between forward and reverse reaction steps that exhibit unimolecular and bimolecular dependences on [catalyst]. Finally, overoxidation of benzyl alcohol to benzoic acid, even at low levels, contributes to catalyst deactivation by formation of a less active palladium benzoate complex. 相似文献