On a new class of function systems of Faber-Schauder type

In this paper, we introduce a new class of function systems generalizing the classical Faber-Schauder system. Under the condition that the generating sequence is bounded, we show that systems of such a class constitute bases in the space of continuous functions and prove some properties of series expansions of functions in these systems.     

Estimates of the rate of convergence of a dynamic reconstruction algorithm under incomplete information about the phase state

In this paper, we study a dynamic reconstruction algorithm which reconstructs the unknown unbounded input and all unobservable phase coordinates from the results of measurements of part of the coordinates. An upper and a lower bound for the accuracy of the reconstruction is obtained. We determine the class of inputs for which the upper bound is uniform. We give a condition for optimally matching the algorithm parameters, ensuring the highest order of the upper bound and equating the orders of the upper and lower bounds. Thus, we establish the sharpness of the upper bound.     

Stereochemical aspects of the formation of toxisterols A

Mechanisms for the formation of toxisterol A are suggested. The connection between the conformation of the initial previtamin and the stereochemistry of the reaction products is discussed.Lensoviet Leningrad Technological Institute. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 225–229, March–April, 1989.     

Mg 2p shallow core-level and local atomic structure of i-ZnMgRE quasicrystals

We present a detailed analysis of the Mg 2p shallow core-levels measured on icosahedral single-grain ZnMgY, ZnMgHo, and ZnMgEr quasicrystals during a photoelectron microscopy study. The synchrotron radiation photoemission measurements were performed on in situ cleaved samples at a pressure of 10⁻¹⁰ mbar and at low temperature, typically 90-150 K. The Mg 2p photoemission lines are essentially broadened as compared to those of the Mg 2p spin-orbit doublet recorded on the Zn₂Mg crystalline Laves phase. The broadening is associated to the coordination shifts of the Mg 2p level due to the inequivalent magnesium sites in the quasicrystalline lattice. The coordination shifts are calculated on the basis of i-ZnMg(Ho, Y) atomic structure data, recently determined from the pair distribution function analysis. The coordination shifts obtained are up to 0.2 eV. The Mg 2p experimental spectral intensity is nicely reproduced by a superposition of coordination-shifted Mg 2p spin-orbit doublets.     

A comparison of spin relaxation and local motion between symmetrically and asymmetrically ring-substituted bisphenol units in dissolved polycarbonates

Carbon-13 and proton spin-lattice relaxation times were measured at two field strengths on solutions 10% by weight of two polycarbonates in C₂D₂Cl₄ from ?20 to +120°C. The first polycarbonate is an asymmetrically substituted form with one chlorine on one of the two phenylene aromatic rings of the bisphenol unit, whereas the second polycarbonate is symmetrically substituted with two chlorines on each of the two rings. The nuclear spin relaxation data are interpreted in terms of several local motions likely in these polymers. Segmental motion was described by the Hall–Helfand correlation function. Segmental motion in the monosubstituted polycarbonate is somewhat slower than in unsubstituted polycarbonate, whereas segmental motion in the tetrasubstituted polycarbonate is considerably slower. Phenylene ring rotation is observed in unsubstituted polycarbonate and in the monosubstituted polycarbonate above 40°C. Below 40°C in the monosubstituted species, and at all temperatures in the tetrasubstituted species, ring rotation is replaced by ring libration as the predominant motion contributing to spin lattice relaxation. In addition, the rotational motion of the two types of rings in the asymmetric monosubstituted form are very similar although not identical. The substituted ring is slightly less mobile than the rings of unsubstituted polycarbonate. This indicates a strong coupling of ring motion, although the coupling leads to less than synchronous motion. Methyl group rotation is present in both polymers and is little affected by the various structural modifications.     

Near-infrared laser photoacoustic detection of methane: the impact of molecular relaxation

A photoacoustic sensor has been developed for trace-gas monitoring using a near-infrared semiconductor laser emitting in the 2ν₃ band of methane at 1.65 μm. The apparatus was designed for on-line process control in the manufacturing of the novel low-water-peak fibres developed for optical telecommunications. The importance of collisional relaxation processes in the generation of the photoacoustic signal is reported in the particular case of CH₄ detection in dry O₂ and O₂–N₂ mixtures. The negative influence of these effects results in a strongly reduced and phase-shifted photoacoustic signal, induced by a fast resonant coupling between the vibrational states of methane and oxygen, associated with the slow relaxation of the excited oxygen molecules. An unusual parabolic response of the sensor with respect to the methane concentration has been observed and is discussed. Finally, the beneficial effect of several species, including water vapour and helium, acting as a catalyst to hasten the relaxation of the CH₄–O₂ system, is demonstrated. PACS 42.62.Fi; 33.20.Ea; 34.50.Ez     

Multiphonon renormalization of the spectrum of two-dimensional excitons in a magnetic field

The renormalization of the dispersion law for two-dimensional excitons in a magnetic field is studied by the Green's-function method taking into account multiphonon processes.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 4, pp. 3–7, April, 1987.