Possibility of observing chiral-symmetry effects in ferromagnetic nanoparticles

The statistics of left-and right-handed vortical magnetization states in a system of submicron-sized ferromagnetic disks is studied experimentally. Lattices of elliptic cobalt particles with a planar size of 750 × 450 nm and a thickness of 25 nm were formed using high-resolution electronic lithography. To visualize the magnetization distributions in the disks, magnetic force microscopy was used. The experimental results indicate the conservation of magnetic chiral symmetry in cobalt ferromagnetic particles of the above size and shape.     

Properties of Josephson junctions in the inhomogeneous magnetic field of a system of ferromagnetic particles

The effect of an array of ferromagnetic nanoparticles on the field-dependent critical current of the short overlap Josephson junction is experimentally studied. Large reversible variations of the maximum critical current are observed depending on the magnetic state of the particles. The pronounced commensurability effects are detected which are proved by the additional peaks of magnetic field induced diffraction pattern.     

Tunnel magnetoresistance of bilayer ferromagnetic nanoparticles with magnetostatic interlayer interaction

A new method for forming submicron magnetic tunnel junctions consisting of two CoFe ferromagnetic layers separated by a dielectric TaO _x spacer is proposed. It is shown that the tunnel magnetoresistance effect can be used for studying the features of magnetization reversal of bilayer ferromagnetic nanoparticles.     

Transition‐State Stabilization by a Secondary Substrate–Ligand Interaction: A New Design Principle for Highly Efficient Transition‐Metal Catalysis

A library of monodentate phosphane ligands, each bearing a guanidine receptor unit for carboxylates, was designed. Screening of the library gave some excellent catalysts for regioselective hydroformylation of β,γ‐unsaturated carboxylic acids. A terminal alkene, but‐3‐enoic acid, was hydroformylated with a linear/branched (l/b) regioselectivity up to 41. An internal alkene, pent‐3‐enoic acid was hydroformylated with regioselectivity up to 18:1. Further substrate selectivity (e.g., acid vs. methyl ester) and reaction site selectivity (monofunctionalization of 2‐vinylhept‐2‐enoic acid) were also achieved. Exploration of the structure–activity relationship and a practical and theoretical mechanistic study gave us an insight into the nature of the supramolecular guanidinium–carboxylate interaction within the catalytic system. This allowed us to identify a selective transition‐state stabilization by a secondary substrate–ligand interaction as the basis for catalyst activity and selectivity.     

Particulars of studying the roughness of substrates for multilayer X-ray optics using small-angle X-ray reflectometry,atomic-force,and interference microscopy

The abilities of standard methods for rough surface investigation are analyzed in case of supersmooth substrates for multilayered X-ray optics. The X-ray specular reflection technique is shown to be the most adequate one. X-ray diffuse scattering and AFM can be applied only in a case of PSD-function calculation and approximation over the entire spectrum range of spatial frequencies.     

Synthesis and photochemical properties of porphyrie-quinone compounds

The results of studies on the synthesis of porphyrin-quinone compounds and investigation of their photochemical properties are summarized. Effects of various factors (the redox potential, the distance between donor and acceptor moieties, their spatial orientation, the free energy of the reaction, and solvents) on the photoinduced electron transfer in these model systems are discussed. The dyad and triad model systems have been compared. The possibility of using these systems for modeling the primary steps of photosynthesis is discussed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1. pp. 9–24, January, 1996.     

In-line and following-up tests of perspective fusion-reactor materials in plasma focus devices

The paper presents results of recent experiments, as performed with the PF-1000 and PF-6 Plasma-Focus facilities, which were aimed at investigation of the correlation between processes of the irradiation of different materials of fusion devices and results of this irradiation. Among the irradiated samples there were pure tungsten, tantalum, copper, aluminum, and alloys, based on these metals, various steels, carbon and carbon-based materials, which are designed for plasma facing components or constructional parts of future thermonuclear reactors of the inertial- and magnetic-confinement types. The corpuscular radiation consisted of high-energy (E _D>100 keV) deuterium ion beams and fast (v _str ≥ 10⁷ cm/s) deuterium-plasma streams. They were investigated by a number of methods with spatial and temporal resolution. Particular attention was paid to the verification of diagnostic techniques, which might be used for time- and space-resolved studies of the interaction process. Correlation of these data with information obtained from subsequent analytical investigation of some of the irradiated specimens, as performed by means of a number of methods typical for material sciences, gives possibility to deduce physical mechanisms of the deuterium implantation and radiation damage of the investigated materials in dependence on the conditions of their irradiation.     

Mn site substitution of La0.67Ca0.33MnO3 with closed shell ions: Effect on magnetic transition temperature

Mn site is substituted with closed shell ions (Al, Ga, Ti, Zr and a certain combination of Zr and Al) and also with Fe and Ru ions carrying the magnetic moment (S=5/2 and 2 respectively) at a fixed concentration of 5 at %. Substitution did not change either the crystal symmetry or the oxygen stoichiometry. All substituents were found to suppress both the metal-insulator and ferromagnetic transition temperatures (T _p(ρ) and T _C, respectively) to varied extents. Two main contributions identified for the suppression are the lattice disorder arising due to difference in the ionic radii between the substituent (r _M) and the Mn³⁺ ion (r _Mn ³⁺) and in the case of the substituents carrying a magnetic moment, the type of magnetic coupling between the substituent and that of the neighboring Mn ion.