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111.
112.
[reaction: see text] Reaction conditions are described for the oxidation of anilines furnishing nitrosoarenes and the synthesis of unsymmetrically substituted azobenzenes. In a comparative study, the catalytic oxidation of methyl 4-aminobenzoate by hydrogen peroxide was investigated, and SeO(2) proved to be superior or equal to methyl trioxorhenium (MTO) and Na(2)WO(4), respectively. Nevertheless, the application of the inexpensive, environmentally friendly, Oxone in a biphasic system proved to be more efficient, and a variety of useful nitrosoarenes for the synthesis of azo compounds were prepared in high yield and purity on a large scale.  相似文献   
113.
The present work describes the first structural studies of protactinium(V) in sulfuric and hydrofluoric acid media using X-ray absorption spectroscopy. The results show unambiguously the absence of the trans-dioxo bond that characterizes the other early actinide elements such as U and Np. In concentrated sulfuric acid (13 M), Pa(V) is proved to exhibit a single oxo bond as postulated in the literature for species in more dilute media. In a 0.5 M HF medium, XANES and EXAFS spectra indicate the absence of any oxo bond: Pa(V) exists in the form of a pure fluoro complex.  相似文献   
114.
The exothermic gas-phase bimolecular nucleophilic substitution (S(N)2) reaction Cl(-)+CH(3)Br (upsilon1',upsilon2',upsilon3')-->ClCH(3) (upsilon1,upsilon2,upsilon3)+Br- and the corresponding endothermic reverse reaction have been studied by time-independent quantum scattering calculations in hyperspherical coordinates on a coupled-cluster potential-energy surface. The dimensionality-reduced model takes four degrees of freedom into account [Cl-C and C-Br stretching modes (quantum numbers upsilon3' and upsilon3); totally symmetric modes of the methyl group, i.e., C-H stretching (upsilon1' and upsilon1) and umbrella bending vibrations (upsilon2' and upsilon2)]. Diagonalization of the Hamiltonian was performed employing the Lanczos algorithm with a variation of partial reorthogonalization. A narrow grid in the total energy was employed so that long-living resonance states could be resolved and extracted. While excitation of the reactant umbrella bending mode already leads to a considerable enhancement of the reaction probability, its combination with vibrational excitation of the broken C-Br bond, (0, 1, 1), results in a strong synergic effect that can be rationalized by the similarity with the classical transitional normal mode. Exciting the C-H stretch has a non-negligible effect on the reaction probability, while for larger translational energies this mode follows the expected spectatorlike behavior. Combination of C-Br stretch and symmetric C-H, (1,0,1), stretch does not show a cooperative effect. Contrary to the spectator mode concept, energy originally stored in the C-H stretching mode is by no means conserved, but almost completely released in other modes of the reaction products. Products are most likely formed in states with a high degree of excitation in the new C-Cl bond, while the internal modes of the methyl group are less important. Reactants with combined umbrella/C-Br stretch excitation, (0, 1, 1), may yield products with two quanta in the umbrella mode.  相似文献   
115.
116.
Ohne Zusammenfassung
Clean-up of plasma samples by column switching techniques: Advantages, limits and problems
  相似文献   
117.

Background  

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder linked to expanded CAG-triplet nucleotide repeats within the huntingtin gene. Intracellular huntingtin aggregates are present in neurons of distinct brain areas, among them regions of adult neurogenesis including the hippocampus and the subventricular zone/olfactory bulb system. Previously, reduced hippocampal neurogenesis has been detected in transgenic rodent models of HD. Therefore, we hypothesized that mutant huntingtin also affects newly generated neurons derived from the subventricular zone of adult R6/2 HD mice.  相似文献   
118.
The chloro and azido complexes trans-[PdCl(4-C5NF4)(PiPr3)2] (3) and trans-[Pd(N3)(4-C5NF4)(PiPr3)2] (4) can be prepared by reaction of [PdF(4-C5NF4)(PiPr3)2] (2) with Et3SiCl or MeSiN3, respectively. In contrast, reactions of 2 with Ph3SiH or Me2FSiSiFMe2 give the products of reductive elimination 2,3,5,6-tetrafluoropyridine (5) or 4-(fluorodimethylsilyl)tetrafluoropyridine (6) as well as [Pd(PiPr3)2] (1). In a catalytic experiment, pentafluoropyridine can be converted with Ph3SiH into 5 in 62% yield, when 10% of 2 is employed as catalyst. Treatment of trans-[PdF(4-C5NF4)(PiPr3)2] (2) with Bu3SnCH=CH2 in THF at 50 degrees C results in the formation of [Pd(PiPr3)2] (1) and 4-vinyltetrafluoropyridine (7). Complex 2 is also active as a catalyst towards a Stille cross-coupling reaction of pentafluoropyridine with Bu3SnCH=CH2 to give 4-vinyltetrafluoropyridine (7) with a TON of 6. The molecular structure of the complex 3 has been determined by X-ray crystallography.  相似文献   
119.
120.
The current flowing across a semiconductor superlattice in tilted electric and magnetic fields is known to exhibit resonant enhancement, when Landau states of neighboring wells align at certain ratios of the field strengths. We show that the ultrafast version of this effect, in which coherent electron wave packets are involved, has a profound analogy to the Fiske effect in superconductor Josephson junctions and superfluid weak links, in that the coupling of the tunneling-induced charge oscillations (magneto-Bloch versus Josephson oscillations) to another oscillator (in-plane cyclotron oscillations versus external oscillator modes) opens an elastic rectifying transport channel. We explore the superlattice effect both theoretically and experimentally, and find that the transient self-induced current can be adequately modeled if the damping of both types of coupled electron oscillations is properly taken into account.  相似文献   
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