Effects of trapped electrons on the line shape in emission Mössbauer spectra

To explain line broadening in emission Mössbauer spectra as compared to the corresponding absorber measurements, the model of trapped electrons has been proposed. Auger electrons (emitted, e.g. after electron capture by ⁵⁷Co or after the converted isomeric transition of ^119mSn), as well as secondary electrons, may be trapped in the proximity to the nucleogenic ion. Electrons captured by lattice traps at different distances from the daughter ion induce an asymmetric distribution of quadrupole splitting in the resulting emission spectra, as shown in a few examples. This model is supported by estimates of quadrupole splitting values which may be caused by such trapped electrons located at specified distances from the nucleogenic atom.     

Mössbauer study of layered iron hydroxysulfides: Tochilinite and valleriite

Natural and synthetic layered iron hydroxysulfides: tochilinite and valleriite, have been investigated by Mössbauer spectroscopy. Tochilinite, magnetite, troilite, and pyrite phases were found in the products of tochilinite synthesis under different conditions. The relative contents of the phases found are determined as functions of the relative magnesium content in the initial mixture. Crystallochemical identification of the ⁵⁷Fe subspectra of valleriite has been performed.     

Subregular Representations of {\mathfrak{s}}{\mathfrak{l}}_n and Simple Singularities of Type A n−1

Alexander Premet has stated the following problem: what is a relation between subregular nilpotent representations of a classical semisimple restricted Lie algebra and non-commutative deformations of the corresponding singularities? We solve this problem for type A.     

Analytical and numerical investigation of the three-dimensional viscous shock-layer on blunt solids

Translated from Zhurnal Prikladnoi Mekhaniki i Tekhnicheskoi Fiziki, No. 4, pp. 81–88, July–August, 1991.     

Phase transition and superconductivity high-T<Subscript>c</Subscript> oxides

On the basis of new experimental studies of specific heat, magnetic properties and thermal expansion, it was shown that dielectric-metal phase transitions were the consequence of delocalization of the heavy holes located on metalapical oxygen bonds in the high-T_c oxide systems. The ordered arrays of such holes (CDW) results in the dielectric gaps in electron spectrum and anomalous negative thermal expansion. The free carriers introduced by doping can couple through excitations of these localized holes, (local bosons). The high-T_c superconductivity will possess anomalous H_c2(T) dependence and γ-type specific heat jump at T_c. This local bosons model is the basis for explanation of the obtained experimental data.     

1,2,4-Triazine and triazole derivatives from α-keto acids and thiosemicarbazides

Thiosemicarbazides of 2-hydroxyphenylglyoxylic acid, which, depending on the conditions, undergo cyclization to interconvertible 5-(2-hydroxyphenyl)-6-oxo-1,2,4-triazine-3-thiones or (2-hydroxy-benzoyl)-²-1,2,4-triazoline-5-thiones, are formed by the action of thiosemicarbazide and its homologs on coumarindione. The thiosemicarbazones of 2-hydroxyphenylglyoxlyic and other 2-substituted phenylglyoxylic acids undergo cyclization to 6-(2-hydroxyphenyl)-5-oxo-1,2,4-triazine-3-thiones.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp, 116–121, January, 1977.     

The photochemical interaction of polyphenylferrisiloxane with oligoorganosilanes

The photochemical interaction of polyphenylferrisiloxane with some oligoorganosilanes in benzene solutions has been studied by UV, IR, ESR, and Mössbauer spectroscopy. Silylene species formed during photolysis of oligoorganosilanes react with the high-spin iron(III) to reduce the latter to low-spin iron(II). The formation of the low-spin state of iron(II) was supported by measurements of the magnetic moments. The insertion of the silylene species into the polymer chain to form the Fe?Si bond occurs due to the photoreaction.     

Polyfunctional compounds containing the 4,6-dialkoxy-7-arylthioheptene moiety as synthetically useful intermediates. The course of lewis acid-induced transformations

Data on the selectivity of the Lewis acids induced transformations of the title compounds are presented, and the routes leading to formation of products containing either cyclohexane or 1,3-diene units are described.