Elektrische Charakterisierung von Hochfrequenz-Niederdruck-Gasentladungen

In recent years there has emerged significant interest in low pressure radio frequency (rf) glow discharges which are used widely particulary in IC fabrication. Various parameters of the rf glow discharge have been found to be useful for its electrical characterization; however, there is no uniformity and agreement. Extensive experimental investigations on various discharge systems have shown, that the self-bias on the rf driven electrode, the complex conductivity and the breakdown characteristic are preferable parameters of rf discharges. Advantageously the self-bias and the complex conductivity should be presented in dependence on the pressure and the applied rf voltage. The discharge current cannot be measured quite accurately due to currents via leaky capacitors and the deviations from a sinusoidal form of the current due to nonlinearities.     

Investigation of the stability of metal species with respect to liquid chromatographic separations

Summary For accurate speciation analyses it is important to know the stability of the respective species, especially in the case of metal complexes. Factors affecting the chromatographic stability of such metal species are investigated. By using thermodynamic models for complex formation and chromatographic retention equilibria the influence of species concentration, stoichiometry and excess of ligand is calculated and compared with experimental results for iron complexes (lactate, gluconate and citrate species). Iron citrate is the only species, that is chromatographed as 1:2 complex (metal: ligand), while iron lactate and gluconate are transformed to 1:1 species. Problems resulting from the coelution of different species are discussed.Dedicated to Professor Dr. Wilhelm Fresenius on the occasion of his 80th birthday     

A Note about the Appearance of Non-Hyperbolic Solutions in a Mechanical Pendulum System

The investigation of the behavior of a nonlinear system consists in theanalysis of different stages of its motion, where the complexity varieswith the proximity of a resonance region. Near this region the stabilitydomain of the system undergoes sudden changes due basically tocompetition and interaction between periodic and saddle solutions insidethe phase portrait, leading to the occurrence of the most differentphenomena. Depending of the domain of the chosen control parameter,these events can reveal interesting geometric features of the system sothat the phase portrait is not capable to express all them, since theprojection of these solutions on the two-dimensional surface can hidesome aspects of these events. In this work we will investigate thenumerical solutions of a particular pendulum system close to a secondaryresonance region, where we vary the control parameter in a restrictdomain in order to draw a preliminary identification about what happenswith this system. This domain includes the appearance of non-hyperbolicsolutions where the basin of attraction in the center of the phaseportrait diminishes considerably, almost disappearing, and afterwardsits size increases with the direction of motion inverted. Thisphenomenon delimits a boundary between low and high frequency of theexternal excitation.     

Buchbesprechungen

Ohne Zusammenfassung     

The crystal and molecular structure of 12,13-dibromopseurotin.

The crystal structure of 12,13-dibromopseurotin has been determined by single crystal X-ray analysis. The crystals belong to space group P2₁ with a = 16.75, b = 9.63, c = 7.42 Å, β 95.9°, Z = 2. The structure was solved by the heavy atom technique and refined to R = 0.062 with 819 significant reflexions for 299 parameters.     

Microchemical investigation of medicinal plants. XV

Summary A method is described for the determination of alkaloids in morning glory leaves by means of spectrophotofluorimetry. The total alkaloidal contents found in different batches of leaves ranged from 0.027 to 0.04%.

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Zusammenfassung Ein Verfahren zur Bestimmung der Gesamtalkaloide in den Blättern vonIpomoea violacea wurde angegeben. Spektralfluoreszenzmessungen ergaben für verschiedene Chargen solcher Blätter Gehalte von 0,027 bis 0,04%.

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For part XIV see Mikrochim. Acta [Wien]1976 I, 227.     

Kinetics of the γ-radiation-induced polymerization of methyl methacrylate in the solid state

Studies have been made of the γ-radiation-induced polymerization of methyl methacrylate in bulk, in the solid state at a temperature of ?65°C. and a radiation intensity of 346,000 rad/hr. The reaction was found to have an extremely long induction period (～50 hr.) when pure monomer was used, and to be first-order with respect to polymer concentration. This first-order dependency was confirmed by a series of irradiations in which 0.6% poly(methyl methacrylate) was dissolved in the monomer before irradiation. These irradiations showed no induction period. Nuclear magnetic resonance spectroscopy indicated a much more heterotactic polymer than that obtained in the liquid state at ?49°C.     

A Study of the 13C NMR Shifts in Two Tetradehydrocyclodecabiphenylenes and Related Aryl and Biphenylenylacetylenes

The ¹³C spectra of 5,6,9,10-tetradehydrocyclodeca[1,2,3,4-def]-benzo [7,8]biphenylene, 1, and 5,6,9,10-tetradehydrocyclodeca [1,2,3,4-def]-naphtho [2,3-7,8]biphenylene, 2, are reported as are those of a number of simpler acetylenic hydrocarbons used as spectral references. Most of the shifts can be assigned unambiguously. The acetylenic shift assignments were verified by ortho-proton, sp-carbon (¹H(1)-¹³C_sp(3)) decoupling experiments. A simple additive shift correlation is found for the hydrocarbons containing unstrained acetylenic groups. However, significant discrepencies are found for the ¹³C shifts for the strained hydrocarbons 1, 2, 1,2-bis(phenylethynyl)-benzene, 12, and 2,3-bis(phenylethynyl)-naphthalene, 13. The discrepencies are particularily large for carbons near the triple bonds and are attributed to a combination of strain, rehybridization, and other proximity effects related to the interaction between the ortho-substituted acetylenic carbons.