Thin-layer chromatographic behaviour and separation of rare earths in silica gel-aqueous alkali metal chloride systems

Summary The thin-layer chromatographic behaviour of all the rare earths except Pm on silica gel in aqueous solutions of five alkali metal chlorides has been surveyed. The Rf-values and the logarithms of the separation factors relative to Gd vary in a regular and peculiar way with increasing atomic number, through a reflection of the strong tetrad effect. A discussion concerning the effects on the Rf-values of the solvent cations and the solvent anions, and typical chromatograms for the separations of multi-component mixtures containing adjacent lanthanoids are also presented.     

Ionization wave as an Instability — Evolution and Nonlinear Effect

Evolution from the linear growth to the nonlinearly saturated state of ionization waves (moving striations) is investigated from a viewpoint of an instability which appears in a plasma. The experiments were performed observing backward waves excited below the upper critical current I_c in xenon, argon, and argon-mercury gases at pressures of the order of Torr. It is found that (1) the behavior of the evolution obeys the Landau amplitude equation; (2) the saturated amplitude does not depend on an initial value, but only on plasma parameters; (3) the linear growth and squared saturation level are proportional to the excess over I_c, and when frequency-controlled, they have a parabolic dependence on the frequency; and (4) nonuniform axial changes in the dc state due to the nonlinear effects appear in a form of enhanced ionization in the plasma where the electron temperature and density are increased. The way of these behavior can be applied to a large number of spatially or temporally unstable modes.     

X-ray photoelectron spectra of nickel halides: multiplet structure and multi-electron excitations in Ni2+ 3p and 2p shells

The satellite structure in the X-ray photoelectron spectra of nickel halides has been measured. The satellites found in the photoelectron spectra of Ni²⁺ 3p and 2p subshells have two common sources: multiples splitting and multi-electron excitations. The experimental spectra are compared with theoretical results on multiples splitting and with calculations of band structure.     

Definite evidences for the population inversion of hot electrons in silver halides

Hot electron kinetics and distribution in pure AgCl and AgBr at crossed electric and magnetic fields have been investigated at 4.2 K up to E_x = 4kVcm^?1 and H_z = 58 kOe, by performing detailed studies of the galvanomagnetic effect in the transient condition. The results of measurements on the tangent of the Hall angle, tan θ, and on the probe current to the hot electron system along the direction of magnetic field, Q_z, established the pictures of an ideal streaming motion of electrons in the range ζ < 1 [where ζV_LO (sE_x/H_z)^?1 and $\text{1}\text{2}\text{m}{}^1\text{V}{}_{\mathrm{<mtext>LO</mtext>}}{}^2\text{}\text{h}\text{?}\text{ω}{}_{\mathrm{<mtext>LO</mtext>}}$] and of a population inversion of hot electrons in the range ζ > 1.     

The crystal and molecular structure of diaquadichlorotheophyllinecopper(II)

Summary The crystal structure of CuCl₂(C₇H₈N₄O₂)(H₂O)₂ has been determined from diffractometer data by Patterson and Fourier methods and refined by full-matrix least-squares to R=0.067 for 2123 observed reflections. Unit cell constants are:a=9.930(8),b=9.987(8),c=7.483(6) Å,=123.2(1),=94.5(1),= 83.9(1)°. The space group is P¯1 withZ=2. The structure consists of diaquadichlorotheophyllinecopper(II) complexes linked by hydrogen bonds. The coordination polyhedron of copper is a square pyramid whose base, severely tetrahedrally distorted, is formed by a water molecule [Cu-Ow=2.025(7) Å], two chlorines [Cu-Cl=2.273(4), 2.296(4) Å] and an imidazole nitrogen [Cu-N=1.983(9) Å] from the theophylline ligand. A second water molecule is at the apex of the pyramid [Cu-Ow=2.292(7) Å]. Coordination is completed to a distorted octahedral one by a long Cu ... O=3.164(7) Å contact involving the exocyclic oxygen at C₆ of the theophylline ligand.