Electronic and magnetic properties of quasifreestanding graphene on Ni

For the purpose of recovering the intriguing electronic properties of freestanding graphene at a solid surface, graphene self-organized on a Au monolayer on Ni(111) is prepared and characterized by scanning tunneling microscopy. Angle-resolved photoemission reveals a gapless linear pi-band dispersion near K[over] as a fingerprint of strictly monolayer graphene and a Dirac crossing energy equal to the Fermi energy (EF) within 25 meV meaning charge neutrality. Spin resolution shows a Rashba effect on the pi states with a large (approximately 13 meV) spin-orbit splitting up to EF which is independent of k.     

Possibilities of surface-sensitive X-ray methods for studying the molecular mechanisms of interaction of nanoparticles with model membranes

The processes of structural rearrangement in a model membrane, i.e., an arachic acid monolayer formed on a colloidal solution of cerium dioxide or magnetite, are studied in situ in real time by the methods of X-ray standing waves and 2D diffraction. It is shown that the character of the interaction of nanoparticles with the monolayer is determined by their nature and sizes and depends on the conditions of nanoparticle synthesis. In particular, the structure formation in the monolayer–particle system is greatly affected by the stabilizer (citric acid), which is introduced into the colloidal solution during synthesis.     

Investigation of the dynamics of the interaction of metal particles with a Langmuir single layer upon an increase in the surface pressure

X-ray studies of dipalmitoylphosphatidylcholine (DPPC) single layers on the surface of a liquid provide detailed information on the interaction of metal particles with a single layer upon an increase in the surface pressure up to the collapse. Two complementary X-ray methods are used: grazing incidence diffraction and the X-ray standing waves method. The experimental results obtained for a single layer formed on a colloidal solution of magnetite nanoparticles reveal that the increase in the surface pressure is accompanied by an increase in the concentration of nanoparticles near the surface. In a series of experiments where metal particles of submicron size are sputtered onto a DPPC single layer, a sharp decrease in the intensity of the fluorescence yield from metal atoms is observed while the single layer is compressed. These data suggest that metal particles deposited onto the surface of a single layer were extruded into the aqueous subphase.     

A representative of p,p,p-trihalogenylides: synthesis and structure

The representative of P,P,P-trichloroylides-5-methyl-2-phenyl-4-(trichlorophosphoranylidene)-2,4-dihydro-3H-pyrazol-3-one-was synthesized. Its constitution was confirmed by 1H, 13C, and 31P NMR spectroscopy and by X-ray analysis. Some chemical properties were studied and compared with ones of P,P,P-trimethylylide-5-methyl-2-phenyl-4-(trimethylphosphoranylidene)-2,4-dihydro-3H-pyrazol-3-one. DFT calculations of the model molecules were carried out.     

Diamondlike nanocomposite a-C:H:Cr Coatings: Structure,mechanical, and tribological properties

The results from a comprehensive investigation of the structure, phase and chemical composition, microhardness, and nanomechanical and tribological properties of chromium-doped coatings of hydrogenised amorphous carbon a-C:H:Cr are presented. The coatings are deposited via reactive magnetron sputtering in an Ar + C₂H₂ + N₂ gas mixture at various volume concentrations of nitrogen and acetylene. It is found that the carbon in the coatings is formed as disordered mixtures of domains with tetrahedral (sp ³) and hexagonal (sp ²) carbon coordinations. In addition, the doping metal in the coating consists of nanosized inclusions of metallic chromium and its carbide and nitride phases. Additional nitrogen doping resulting in the formation of chromium nitride is shown to improve the micromechanical and tribological properties of the obtained coatings.     

Spatial confinement of ferromagnetic resonances in honeycomb antidot lattices

We report on a theoretical investigation of the magnetic static and dynamic properties of a thin ferromagnetic film with honeycomb lattice of circular antidots using micromagnetic simulations and analytical calculations. The theoretical model is based on the Landau–Lifshitz equations and directly accounts for the effects of the magnetic state nonuniformity. A direct calculation of local dynamic susceptibility tensor yields that the resonance spectra consist of four different quasi-uniform modes of the magnetization precession related to the confinement of magnetic domains by the hole mesh. Three of four resonant modes follow a two-fold variation with respect to the in-plane orientation of the applied magnetic field. The easy axes of these modes are mutually rotated by 60° and combine to yield the apparent six-fold configurational anisotropy. Additionally, a mode with intrinsic six-fold symmetry behavior exists, as well. Micromagnetic calculations of the local dynamic susceptibility tensor allow identifying the magnetic unit cell areas/domains responsible for each resonance mode.     

Synthesis, X-Ray Diffraction Data, and 1H and 13C NMR Spectra of N-(N-Arylsulfonylimidoyl)-1,4-benzoquinonimines Derived from N-Aroyl(acetyl)-1,4-benzoquinonimines

Oxidation of N-(N-arylsulfonylimidoyl)-4-aminophenols gave the corresponding N-[N-arylsulfonylimidoyl)-1,4-benzoquinonimines, derivatives of N-aroyl- and N-acetyl-1,4-benzoquinonimines. The structure of the products was studied by the X-ray diffraction method and ¹H and ¹³C NMR spectroscopy. N-(N-Arylsulfonylimidoyl)-1,4-benzoquinonimines were found to undergo fast (on the NMR time scale) Z E isomerization about the CÍN bond in the quinonimine fragment. N-(N-Arylsulfonylacetimidoyl)-1,4-benzoquinonimines in solution give rise to dynamic Z E-isomerization with respect to the CÍN bond in the N-arylsulfonylacetimidoyl fragment.     

Facile synthesis of C-phosphanylformamidines via a carbene pathway

A direct synthetic approach to C-phosphanyl-N,N-dialkyl-N′-aryl(alkyl)-formamidines was developed. It was shown that phosphorylation of the formamidines proceeds at the nitrogen atom affording N-phosphanylformamidinium salts. Upon deprotonation, these salts gave C-phosphanylformamidines via formation of carbenes followed by a 1,2-phosphorus shift.