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1.
Journal of Solid State Electrochemistry - The electrochemical deposition of a nickel–iron alloy from a plating solution based on a deep eutectic solvent (a eutectic mixture of ethylene glycol...  相似文献   
2.
Herein, we report an addition to the toolbox for the monitoring and quantification of the hydrolytic decay of pentose-1-phosphates, which are known to be elusive and difficult to quantify. This communication describes how apparent equilibrium shifts of a nucleoside phosphorolysis reaction can be employed to calculate hydrolytic loss of pentose-1-phosphates based on the measurement of post-hydrolysis equilibrium concentrations of a nucleoside and a nucleobase. To demonstrate this approach, we assessed the stability of the relatively stable ribose-1-phosphate at 98 °C and found half-lives of 1.8–11.7 h depending on the medium pH. This approach can be extended to other sugar phosphates and related reaction systems to quantify the stability of UV-inactive and hard-to-detect reaction products and intermediates.  相似文献   
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A first example of an Et2Zn mediated silylation of 1-aklynes is reported. A series of functional groups are tolerated in this reaction. Mechanistic studies support Zn alkynilides as intermediates in the reaction. This reaction protocol provides a practical method for the preparation of alkynylsilanes and expands the application of organometallic zinc in organic synthesis.  相似文献   
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We prove stability of rotationally symmetric translating solutions to mean curvature flow. For initial data that converge spatially at infinity to such a soliton, we obtain convergence for large times to that soliton without imposing any decay rates. The authors are members of SFB 647/B3 “Raum – Zeit – Materie: Singularity Structure, Long-time Behaviour and Dynamics of Solutions of Non-linear Evolution Equations”.  相似文献   
7.
Let X be a 1-connected CW-complex of finite type and ε?(X) be the group of homotopy classes of self-equivalences of X which induce the identity on homotopy groups. In this paper, we prove that every finitely generated 2-solvable rational nilpotent group is realizable as ε?(X) where X is the rationalization of a 1-connected CW-complex of finite type.  相似文献   
8.
Consider two copies N1, N2 of the interval [0, ∞]. Consider Klein-Gordon equations with (different) constant coefficients on ? × Nj ( = time × space). Assume the coincidence of the values of the solution at the boundary points of the Nj for all times and a transmission condition relating its first (one-sided) space derivatives at these points. Under a symmetry condition, we extend the spatial part of the equation and the transmission conditions to a self-adjoint operator (by Friedrichs extension) and reformulate our problem in terms of an abstract wave equation in a suitable Hilbert space. We derive an expansion of the solution in generalized eigenfunctions of this self-adjoint extension and show, that the L-norms (in space) of the solution and its first k space derivatives at the time t decay for t → ∞ at least as const. t¼, if the initial conditions satisfy a compatibility condition of order k derived in this paper. The loss of decay rate in comparison with the full line case (const. t, cf. [28]) is caused by the tunnel effect. Further we show that an abstract wave equation in a Hilbert space with a Friedrichs extension as spatial part can always be derived from a stationarity principle for an associated action-type functional. This yields a physical legitimation of our model by the principle of stationary action and moreover a criterion for the physical interpretability of all models created by the linear interaction concept [4, 6, 8, 10], in particular for the coupling of media of different dimension (alternative to [13, 16] for similar models).  相似文献   
9.
Summary A method has been developed for extraction and determination of carbofuran in milk. The method involved direct injection of raw milk on to a human serum albumin dimethyloctyl-silica gel (HSA-C8) column and the use of 80:20 (v/v) 0.01 M phosphate buffer pH 5.5-acetonitrile as mobile phase. UV spectrophotometric detection was performed at 220 nm. Identification was based on retention time. Quantification was performed by automatic peak-area determination and was calibrated by use of an external standard.  相似文献   
10.
Three Pt-based catalysts prepared in different radiolytic conditions and supported on graphite powder were packed into a carbon paste electrode configuration. They were compared to each other, to the commercial (Pt) deposited on activated carbon powder (Johnson Matthey) and to pure Vulcan XC-72 for their respective abilities toward the hydrogen evolution reaction (HER). The Tafel parameters were determined for all these electrodes. From the I–V curves and their quantitative treatment, the following order of activity emerged unambiguously and reads: (PtCO)2 (fcc structure) > (PtCO)1 (Chini cluster) > (Pt)neat > (Pt)JM (Johnson Matthey) ≫ (Vulcan XC-72). As expected, all the Pt-loaded electrodes were more efficient than Vulcan XC-72. The classification appears to be linked with the mean nanoparticle size, and for comparable sizes, with the surface morphology of the materials. The results and the stability of the electrodes suggest that the small particle sizes and the good dispersity on the carbon support were maintained during the HER.  相似文献   
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