On the magneto-optics of orthoferrites with spin reorientation

The results of magneto-optical investigations into the Γ₂–Γ₄ spin reorientation in an Sm_0.6Tb_0.2Tm_0.2FeO₃ orthoferrite single crystal are reported. The magneto-optical parameters are determined taking into account the dichroism. The orientation of the antiferromagnetic vector in the canted phase is investigated as a function of the magnetic field and temperature. The magnetic anisotropy field strengths are determined by the processing of the results. The orientation contribution to the birefringence is estimated.     

Synthesis and structure of nanocrystalline La0.50Ba0.50MnO3

Nanocrystalline manganite La_0.50Ba_0.50MnO₃ was synthesized by the soft-chemical method. For this purpose, the sol-gel method was modified and improved. A trihydric saturated alcohol, e.g., glycerol, was suggested as a new organic matrix. The crystal structure of the composite was studied by X-ray powder diffraction at room temperature. A La_0.50Ba_0.50MnO₃ powder annealed in air at T = 500°C is characterized by a perovskite-like cubic structure with the unit-cell parameter a = 3.869 Å. The chemical composition of the sample was studied by electron-probe X-ray microanalysis. The La: Ba: Mn cation ratio in the material was 1: 1: 2. The surface topography was examined with a scanning electron microscope. The crystallite size was ～30 nm. The dependence of the crystal structure and the surface topology on the annealing temperature was studied. The high-temperature treatment in air resulted in the growth of larger, micrometer-size, crystallites.     

Structural investigations in the series of spiro(thia)chromans

A comparative assessment was made of the reactivity of carbonyl-containing spirohydrochromans in their reaction with hydrogen sulfide under the conditions of acid catalysis. The special features of the structure of one of the obtained condensed spiro(thia)chromans are examined on the basis of the results from x-ray crystallographic analysis, the¹³C NMR spectra, and quantum-chemical calculations. N. G. Chernyshevskii Saratov State University, Saratov 410026, Russia. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1340–1345, October, 1998.     

Reactions of Fused Carbonyl-containing Spirodihydrofurans with Hydrogen Sulfide and Acids

Reactions were studied of fused spirodihydrofurans originating from 1,3-cyclohexanedione with hydrogen sufide arising in situ. Depending on a substituent at the atom C ³ of the heterocycle the reaction ended by thionation of the conjugated carbonyl group followed by heterocyclization involving the spirodimedonyl fragment. A quantum-chemical forecasting of the protonation stages of substrates and their thionated analogs was performed applying the semiempirical PM3 procedure. A probable mechanism of investigated transformations of the spirodihydrofurans was suggested.     

Influence of the position of the nitro group on the structural and spectroscopic characteristics of N"-(nitrobenzylidene)isonicotinic hydrazides in the crystalline state

N"-Substituted isonicotinic hydrazides of the general formula Py—C(=O)—N(H)-N"=C(H)—R, where R is o- (1), m- (2), or p-nitrophenyl (3), were studied by IR spectroscopy and X-ray diffraction analysis. The position of the nitro group in these compounds has no effect on the type of the crystal structure. The crystal packings are based on stacks consisting of antiparallel planar molecules. The molecules from the adjacent stacks are linked to each other via the N—H...N_Py hydrogen bonds. Depending on the position of the nitro group, the N...N_Py distance increases in the series 3 > 1 > 2 and the energy of the hydrogen bonds decreases (according to the IR spectroscopic data) from 3.9 to 3.1 kcal mol^–1. Analysis of the IR spectra demonstrated that the intensity of absorption in the (C—H) stretching region of the pyridine ring increases substantially as the the N—H...N_Py hydrogen bond is strengthened. Some regularities of the changes, which are observed for the (NO₂) bands in the spectra of the nitrophenyl-containing conjugated molecules in solutions, persist in the crystalline state.     

Effect of oxygen pressure on phase composition and magnetic structure of FeCoZr-Pb(ZrTi)O3 nanocomposites

The elemental and phase compositions and the magnetic state of metal particles in FeCoZr-Pb(ZrTi)O₃ granular nanocomposites (GNCs) synthesized by ion-beam sputtering of composite targets in oxygen-containing media at different oxygen partial pressures have been studied. The phase transformations in GNCs have been monitored by the Raman and M?ssbauer spectroscopy techniques. Correlation between the oxygen pressure during GNC synthesis and the valence state of iron ions in metal granules has been established. It has been confirmed that (i) the degree of metal oxidation increases with increasing oxygen pressure and (ii) the degree of crystallinity of oxides increases as a result of annealing. It has been established that the percolation threshold in GNCs can also be varied by changing the oxygen pressure during GNC synthesis.     

Effect of Magnetic Co–CoO Particles on the Carrier Transport in Monolayer Graphene

Physics of the Solid State - Electrodeposition of cobalt on monolayer graphene synthesized by chemical vapor deposition produces Co–CoO/graphene composite structures, which is accompanied by...     

Triplet States of Cyanine Dye Dimers

Russian Physics Journal - The results of investigations of the properties of cyanine dye dimers in the triplet state are presented. The formation of dimers is demonstrated as two absorption bands...