Temporal evolution of a long-pulse high-density electron beam

The temporal evolution of a long-pulse high-density electron beam in a high-power traveling-wave tube with a periodic magnetic focusing system is investigated. The relation between the variation of the characteristics of the electron beam and ionization of the residual gas and particles desorbed from the electrode surfaces is shown. A strong influence of the formation of the collector plasma and the flux of ions from its surface on the beam dynamics is revealed. The effect of microwave fields in the transport channel on the characteristics of the beam during its evolution is studied. Zh. Tekh. Fiz. 67, 54–58 (December 1997)     

Measurement of the differential cross section and of the tensor and vector analyzing powers for the fragmentation of 4.5-GeV/c deuterons on beryllium in the reaction involving proton emission at an angle of 80 mrad

The invariant differential cross section, the tensor analyzing power A _yy , and the vector analyzing power A _y for the reaction ⁹Be(d, p)X are measured at an initial deuteron momentum of 4.5 GeV/c and a proton detection angle of about 80 mrad. The data obtained for the differential cross section are consistent with the results of measurements at 3.5 and 5.78 GeV/c and a proton emission angle of 2.5°. The values found for the tensor analyzing power A _yy are compared with similar data obtained previously for the deuteron-fragmentation process occurring on a carbon target at various values of the initial deuteron momentum and leading to proton emission at zero angle. The data on the differential cross section for the reaction ⁹Be(d, p)X can be satisfactorily described within the relativistic impulse approximation by using standard deuteron wave functions; however, the approach based on this conceptual framework proves to be inadequate in dealing with data on the tensor analyzing power. These results indicate that it is necessary either to change the method for describing the relativistic deuteron or to take into account additional mechanisms.     

Nuclear superstructure {1/2, 0, 1/2} of an La<Subscript>0.93</Subscript>Sr<Subscript>0.07</Subscript>MnO<Subscript>3</Subscript> manganite orthorhombic crystal

The {1/2, 0, 1/2} nuclear superstructure in an La_0.93Sr_0.07MnO₃ manganite orthorhombic crystal is revealed using thermal-neutron diffraction. It is demonstrated that this superlattice belongs to the class of distortion-type structures and is directly associated with a 1/16-type ordering of Mn⁴⁺ and Mn³⁺ ions in a collinear ferromagnetic phase of the La_0.93Sr_0.07MnO₃ manganite.     

Magnetic structure and transport properties of atomically disordered crystals of two-dimensional manganites La2−2x Sr1+2x Mn2O7

The magnetic structure and transport properties of partially disordered crystals of two-dimensional manganites La_2?2x Sr_1+2x Mn₂O₇ (x = 0.3, 0.4) are studied over a wide range of temperatures. The crystals are transformed into an atomically disordered state under irradiation with fast neutrons at a dose of 2 × 10¹⁹ cm^?2. The average concentration of substitutional defects in the crystal is ≈4%. It is found that substitutional defects are responsible for the transition of these manganites from the ferromagnetic metal state to the insulator state with a spin glass structure. The results obtained are discussed in terms of the ratio between the kinetic energy of charge carriers and the exchange energy of localized spins.     

Synthesis and structural characterization of carbon-centered tris(pentafluorophenyl)silyl derivatives

A general method for the synthesis of carbon-centered tris(pentafluorophenyl)silyl derivatives (RSi(C₆F₅)₃) by reaction of trichlorosilanes (RSiCl₃) with pentafluorophenylmagnesium bromide was described. The crystal structures of obtained compounds were studied by X-ray diffraction analysis (7 structures). The peculiarities of crystal packing were analyzed by means of DFT calculations.     

Determination of the Isotopic and Elemental Composition of the Core of an Armor-Piercing Projectile

The elemental and isotopic composition of the core material of a hard-core projectile that had fallen onto the ground was studied by secondary-ion mass spectrometry, alpha and gamma spectrometry, X-ray photoelectron spectroscopy, and scanning electron microscopy with X-ray microanalysis. The environmental aspect of the use of depleted uranium ammunition in Yugoslavia is discussed.     

Mean value of weyl sums

We give a simple proof of a mean value theorem of I. M. Vinogradov in the following form. Suppose P, n, k, τ are integers, P≥1, n≥2, k≥n (τ+1), τ≥0. Put $$J_{k,n} (P) = \int_0^1 \cdots \int_0^1 {\left| {\sum\nolimits_{x = 1}^P {e^{2\pi i(a_1 x + \cdots + a_n x^n )} } } \right|^{2k} da_1 \ldots da_n .} $$ Then $$J_{k,n} \leqslant n!k^{2n\tau } n^{\sigma n^2 u} \cdot 2^{2n^2 \tau } P^{2k - \Delta } ,$$ where $$\begin{gathered} u = u_\tau = min(n + 1,\tau ), \hfill \\ \Delta = \Delta _\tau = n(n + 1)/2 - (1 - 1/n)^{\tau + 1} n^2 /2. \hfill \\ \end{gathered} $$      

Reactions of salicylaldehyde with tris(pentaf luorophenyl)silanes and secondary amines

Reactions of tris(pentafluorophenyl)silanes RSi(C₆F₅)₃ with salicylaldehyde and secondary amines were studied. The reactions afforded α-pentafluorophenyl-substituted amines. Silanes RSi(C₆F₅)₃ (R = Me, Ph, C₆F₅, CH₂CH=CH₂, and CH=CH₂) were found to be efficient reagents for transfer of the C₆F₅ group to the iminium cation generated from salicylaldehyde and amine. However, tris(pentafluorophenyl)phenylethynyl-and tris(pentafluorophenyl)silanes were not able to serve as a source of a fluorinated substituent because of competitive transfer of acetylenide fragment or hydride. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 498–503, March, 2006.