Quantitative Depth Profiling of K-Doped Fullerene Films Using XPS and SIMS

 Phenomena accompanying electrochemical doping of solid fullerene films with potassium were studied by sputter ion depth profiling (XPS and SIMS). The potassium distribution was determined, and artifacts associated with possible damage of the layer composition caused by ion impact were investigated and discussed. To compare the charge transfer while reductive doping is taking place at fullerene/solution interface with doping from gas phase, model layers were prepared and doped by potassium under UHV conditions. It was found that sputtering by Ar⁺ primary ions yields both accurate information on the alkaline metal distribution and on its concentration. Sputtering by O⁺ ions led to an enrichment of potassium, apparently due to the reactivity of oxygen with the fullerene matrix. It is shown that the reductive doping starts at the fullerene/solution interface. The concentration of potassium in the doped films was found to be lower than expected from the charge transferred during the electrochemical reduction. Other phase transformations such as hydrogenation are discussed. Received March 4, 2002; accepted July 26, 2002     

On formal integration in composition rings of polynomials

This author wants to express his thanks to the School of Information Engineering at Teesside Polytechnic, Middlesbrough, England, for its support and hospitality during a visiting appointment of 3 months in 1989, when this paper was written.     

Einige Winke zur Beschleunigung der Stickstoffanalyse

Ohne Zusammenfassung     

Spreading of a smectic A liquid crystal on a rotating disc

We describe the dynamics of spreading of a smectic A liquid crystal deposited on a rotating disc. We show the existence of several regimes according to the film thickness. If it is thick enough, the thinning is controlled by bulk permeation; at intermediate thicknesses the surface dissipation dominates, whereas viscous effects begin to be felt only at very small thickness.     

Measurement ofD(\vec p,p)D elastic scattering at 10.0, 12.0, 14.1 and 16.5 MeV especially for small forward and extreme backward scattering angles

The elastic scattering was investigated especially in the Coulomb sensitive scattering regions. Angular distributions of the differential cross section and of the analyzing powerA _y, with emphasis on small scattering angles, were measured at 10.0 and 14.1 MeV. For extreme backward angles up toJ _c.m.=179° the differential cross section was measured at 12.0, 14.1 and 16.5 MeV. The data have been compared with recent Faddeev calculations based on the realistic meson-exchange Paris potential and including an approximate Coulomb correction. There are discrepancies between the data and the calculations especially for the analyzing power. This indicates that the approximate treatment of Coulomb effects and possibly also the purely nuclear part of the calculations need to be improved.     

On a characterization of the normal distribution by means of identically distributed linear forms

Let X₁, X₂,…, be independent, identically distributed random variables. Suppose that the linear forms L₁ = Σ_j=1^∞a_jX_j and L₂ = Σ_j=1^∞b_jX_j exist with probability one and are identically distributed; necessary and sufficient conditions assuring that X₁ is normally distributed are presented. The result is an extension of a theorem of Linnik (Ukrainian Math. J.5 (1953), 207–243, 247–290) concerning the case that the linear forms L₁ and L₂ have a finite number of nonvanishing components. This proof only makes use of elementary properties of characteristic functions and of meromorphic functions.     

The 6Li,6Li-INADEQUATE Experiment: A New Tool for 1D- and 2D-NMR Studies of Organolithium Compounds

The 1D- and 2D-⁶Li, ⁶Li-INADEQUATE experiments are described as new tools for the detection of scalar coupled nonequivalent ⁶Li nuclei in organolithium clusters. Practical applications of these sequences are demonstrated for the ⁶Li-NMR spectra of (E)-1-lithio-2-(2-lithiophenyl)-1-phenylhex-1-ene ( 1 ) and (E)-2-lithio-1-(2-lithiophenyl)-1-phenylpent-1-ene ( 2 ), where signals due to dimers and monomers can be distinguished. The performance of the 2D-⁶Li, ⁶Li-INADEQUATE and the ⁶Li, ⁶Li-COSY-45-LR experiment are compared. The ⁶Li chemical shifts of 1 and 2 are discussed.