Intensity of Ar spectral lines in an Ar-O2 glow discharge

Measurements of relative intensities of spectral lines and of plasma parameters have been carried out in an Ar-O₂ d.c. glow discharge under the following conditions: gas pressures of 1, 2 and 3 torr and partial pressures for O₂ of 0, 0.01, 0.02, 0.05 and 0.1 torr. Many of the Ar line intensities decreased when O₂ was added, while some were enhanced. Enhancement of the 6677A and 7504A lines has been most notable. The number density of metastable Ar atoms is decreased when O₂ is added. Upon addition of O₂, the electron temperature is decreased and the electron density increased, except at a gas pressure of 1 torr; the electric field strength in the positive column is also increased.     

Low temperature magnetic properties of trimeric clusters

The degeneracy in the Heisenberg model of the three chromium clusters having D₃ symmetry is split by the antisymmetric exchange interaction. Based on this new energy level scheme, the low temperature behavior of the specific heat and magnetic susceptibility are reexamined.     

Symmetries and conservation laws of the classical Boussinesq equation

A recursion operator for the classical Boussinesq equation is given, which yields infinitely many symmetries and conservation laws. It is also shown that these symmetries define a hierarchy of the classical Boussinesq equation each of which is a hamiltonian system.     

Formation of cyclic organosilicon compounds via organopolysilyl anions starting from methoxymethyldisilanes. A mechanistic study

In the presence of a catalytic amount of sodium methoxide, sym-dimethoxytetramethyldisilane was converted into α,ω-dimethoxypermethylpolysilanes, MeO(SiMe₂)_nOMe where n ? 3, at room temperature. On the other hand, similar treatment of the disilane in THF solution gave cyclic polysilanes, (Me₂Si)_n where n = 5–7. Decomposition of the disilane in the presence of diphenylacetylene afforded a trisilacyclopentene derivative under similar conditions. This compound was obtained also by the reaction between α,ω-dimethoxypermethylpolysilanes and diphenylacetylene in the presence of sodium methoxide. These cyclic products most likely were formed via permethyl polysilyl anion intermediates derived from α,ω-dimethoxypermethylpolysilanes. Also, the formation of α,ω-dimethoxypermethylpolysilanes could be elucidated in terms of the mechanism involving the base-assisted, concerted nucleophilic substitution or stepwise substitution by silyl anions, rather than the successive dimethylsilylene (Me₂Si:) insertion reaction.     

Experimental determination of chlorine isotope separation factor by anion-exchange chromatography

Chlorine isotope fractionation factor was determined by strongly basic anion-exchange chromatography with 0.1 mol/l HCl at 25 °C. The magnitude of the factor was calculated as a single-stage separation factor of 1.00030 with analytical precision of 0.00006 (1σ). The results showed that the lighter isotope () was preferentially fractionated into the resin phase, while the heavier one () enriched into the aqueous phase. This trend suggested that the hydrated Cl⁻ ions in the aqueous phase were slightly more stable than the hydrated Cl⁻ ions electrostatically interacting with the ion-exchange groups of the resin.     

Isolable anion radical of blue disilene (tBu2MeSi)2Si=Si(SiMetBu2)2 formed upon one-electron reduction: synthesis and characterization

The highly twisted tetrakis(di-tert-butylmethylsilyl)disilene 4 was prepared and reacted with (t)BuLi in THF, producing disilene anion radical 5 upon one-electron reduction. The anion radical 5 was isolated in the form of its lithium salt as extremely air- and moisture-sensitive red crystals. The molecular structure of 5 was established by X-ray crystallography, which showed a nearly orthogonal structure (twisting angle of 88 degrees ) along the central Si-Si bond, with a length of 2.341(5) A, which is 3.6% elongated relative to that of 4. The interesting feature of 5 is that one of the central Si atoms has radical character, whereas the other Si atom has silyl anion character. An electron spin resonance (ESR) study of the hyperfine coupling constants of the (29)Si nuclei indicates that rapid spin exchange occurs between these central Si atoms on the ESR time scale.