Neutron interferometry in gravitational field with torsion

We consider the possibility of finding experimental evidence of the fifth force with the measurement of a phase shift of neutron beams via an interferometric apparatus and also a possible rotation of the polarization plane of polarized neutron beams when torsion is introduced in a gravitational field.     

Gauge Dependence of the Effective Gravitational Field

We analyze the gauge ambiguity problem for the effective gravitational field from the standpoint of the measurement process. The motion of a test point particle playing the role of a measuring device is investigated in the field of a point gravitating mass in the one-loop approximation. We show that the gravitational field value determined from the effective equations of motion of the device explicitly depends on the Feynman gauge parameter. This dependence is essential in the sense that a gauge variation cannot be interpreted as a deformation of the reference frame, which leads to a gauge ambiguity in the values of observed quantities. In particular, this result disproves the hypothesis that gauge dependence is canceled in the effective equations of motion of a classical point particle.     

Electron focusing in backscattering from single-crystal Si(100)

Diffraction patterns produced by quasi-elastically backscattered electrons focused in a thin single-crystal Si(100)2×1 near-surface layer have been studied. The measurements performed in the 0.6–2-keV range are compared with calculations made in the single-scattering cluster approximation. This model is shown to describe adequately the experiment. An analysis is made of the relation among the diffraction patterns observed for different silicon faces, and of the effect of the primary-electron beam orientation. The relations governing the focusing of quasi-elastically backscattered electrons escaping from the crystal along the main crystallographic directions have been established. The various aspects of the effect for backscattered electrons undergoing inelastic interaction with the electron subsystem of the crystal have been investigated. Fiz. Tverd. Tela (St. Petersburg) 40, 1364–1369 (July 1998)     

One-loop divergences of linear gravity with torsion terms

We investigate the role of the torsion field at the quantum level. One-loop counterterms are calculated in the theory with terms quadratic in the torsion field. We have shown that the theory is finite at the one-loop level.     

Role of the 3d orbitals of sulfur in the thiapyrylium cation

The electronic structure of the thiapyrylium cation with allowance for and neglect of the 3d orbitals of sulfur was investigated by the self-consistent field MO LCAO method within the CNDO/2 (complete neglect of differential overlap) approximation. Inclusion of the 3d AO of sulfur in the basis leads to slight redistribution of the electron density to favor equalization of the charges on the carbon atoms. A qualitative correlation of the calculated populations of the atoms with the chemical shifts of the PMR spectrum of the thiapyrylium cation was obtained.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1627–1629, December, 1976.     

Investigation of the lability of furan and its derivatives in nucleophilic substitution reactions by the mindo/3 method

The a complexes of furan, thiophene, pyrrole, pyridine, and benzene with the hydride ion were calculated by the MINDO/3 method. The affinities of the indicated aromatic rings and a number of substituted furans for the H^– ion were estimated. It is shown that the relative magnitude of the affinity correlates qualitatively with the experimental data on the relative rates of the reaction of the examined compounds with nucleophilic reagents. The following order of increasing reactivities of unsubstituted aromatic rings was obtained: pyrrole相似文献   

Synthesis of cationic complexes [(C<Subscript>4</Subscript>Me<Subscript>4</Subscript>)CoL]<Superscript>+</Superscript> (L is naphthalene,phenanthrene, and anthracene)

Cationic arene complexes [Cb*Co(naphthalene)]⁺ (2, Cb* = C₄Me₄) and [Cb*Co(phenanthrene)]⁺ were synthesized by the reactions of [Cb*Co(MeCN)₃]⁺ with arenes. The [Cb*Co(anthracene)]⁺ complex was synthesized by the abstraction of the iodide ion from [Cb*CoI]₂ by TIBF₄ in the presence of anthracene. Complex 2 exchanges the naphthalene ligand for other arenes at room temperature. Dedicated to Academician G. A. Abakumov on the occasion of his 70th birthday. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1861–1863, September, 2007.     

Electronic and Magnetic Structure of Intercalated Graphene Films

Physics of the Solid State - Ab initio calculations of the electron spectrum of the graphene–cobalt–nickel system were performed in the slope of the spin density functional theory...     

Influence of high-temperature annealing on the orientation of the unipolarity vector in lead zirconate titanate thin films

The factors responsible for the change in the orientation of the natural unipolarity vector due to heating to the Curie temperature of a Pt/PZT/Pt thin-film capacitor (PZT—lead zirconate titanate) formed on a TiO₂/SiO₂/Si substrate have been considered. Lead zirconate titanate thin layers containing a small excess of lead oxide have been formed ex situ using high-frequency magnetron sputtering with a variation in the annealing temperature (crystallization of the perovskite phase) in the range from 580 to 650°C. It has been assumed that the reorientation of the unipolarity vector in the PZT layer is caused by the change in the mechanism of crystallization of the perovskite phase with an increase in the annealing temperature.     

Cyanide Complexes Based on {Mo6I8}4+ and {W6I8}4+ Cluster Cores

Compounds based on new cyanide cluster anions [{Mo₆I₈}(CN)₆]^2–, trans-[{Mo₆I₈}(CN)₄(MeO)₂]^2– and trans-[{W₆I₈}(CN)₂(MeO)₄]²⁻ were synthesized using mechanochemical or solvothermal synthesis. The crystal and electronic structures as well as spectroscopic properties of the anions were investigated. It was found that the new compounds exhibit red luminescence upon excitation by UV light in the solid state and solutions, as other cluster complexes based on {Mo₆I₈}⁴⁺ and {W₆I₈}⁴⁺ cores do. The compounds can be recrystallized from aqueous methanol solutions; besides this, it was shown using NMR and UV-Vis spectroscopy that anions did not undergo hydrolysis in the solutions for a long time. These facts indicate that hydrolytic stabilization of {Mo₆I₈} and {W₆I₈} cluster cores can be achieved by coordination of cyanide ligands.