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31.
Ivanova  M. V.  Ushakov  V. I. 《Mathematical Notes》2002,72(1-2):43-47
This paper is devoted to the study of the solvability of the second mixed problem in a noncylindrical domain for the nonstationary equation $${\text{div}}(k(x){\text{ grad }}u_t ) - c(x)u_t - b(x)u(x,t) = f(x,t)$$ called the pseudoparabolic equation. We prove existence and uniqueness theorems for the solution in the case of contracting (as time t increases) domains.  相似文献   
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For doped semiconductor superlattices we have analyzed the effects of absorption saturation and change in the refractive index depending on the level of their excitation and structure parameters. The calculations were carried out with account for the tails of the density of states and screening of the electrostatic potential. It is shown that doped superlattices may display shading, i.e., the increase in the absorption coefficient at a fixed frequency with increase in light intensity. For –doped superlattices a stronger nonmonotonicity of the change in the refractive index with increase in the excitation level in comparison with typical structures can manifest itself.  相似文献   
34.
For two periods of quantum-cascade laser structures, we propose a system of closed balance equations that make it possible to calculate the occupancy of the energy levels, the quasi-Fermi levels, and also the injection current density taking into account different charge carrier scattering mechanisms. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 6, pp. 801–804, November–December, 2007.  相似文献   
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The 1H, 13C and 15N NMR studies have shown that the E and Z isomers of pyrrole‐2‐carbaldehyde oxime adopt preferable conformation with the syn orientation of the oxime group with respect to the pyrrole ring. The syn conformation of E and Z isomers of pyrrole‐2‐carbaldehyde oxime is stabilized by the N? H···N and N? H···O intramolecular hydrogen bonds, respectively. The N? H···N hydrogen bond in the E isomer causes the high‐frequency shift of the bridge proton signal by about 1 ppm and increase the 1J(N, H) coupling by ~3 Hz. The bridge proton shows further deshielding and higher increase of the 1J(N, H) coupling constant due to the strengthening of the N? H···O hydrogen bond in the Z isomer. The MP2 calculations indicate that the syn conformation of E and Z isomers is by ~3.5 kcal/mol energetically less favorable than the anti conformation. The calculations of 1H shielding and 1J(N, H) coupling in the syn and anti conformations allow the contribution to these constants from the N? H···N and N? H···O hydrogen bondings to be estimated. The NBO analysis suggests that the N? H···N hydrogen bond in the E isomer is a pure electrostatic interaction while the charge transfer from the oxygen lone pair to the antibonding orbital of the N? H bond through the N? H···O hydrogen bond occurs in the Z isomer. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   
37.
A universal approach to the molecular design of light-sensitive nanodimensional systems with specific characteristics was developed on the basis of unsaturated and macrocyclic compounds. It was possible to construct various nanodimensional systems within the scope of a single class of compound using a limited number of components. The use of photostructural transformations to control complex formation and mechanical movements in molecular devices and machines is discussed. Translated from Teoreticheskaya i éksperimental’naya Khimiya, Vol. 45, No. 1, pp. 1–7, January-February, 2009.  相似文献   
38.
It has been shown that a composite film activated by spherical nanoparticles can ensure ideal optical antireflection when the amplitude of the transmitted light wave is equal to the amplitude of the external wave at various angles of incidence independently on the optical properties of the underlying medium. The amplitude of the reflected wave vanishes in a wide range of optical wavelengths. It has been shown that the effect of ideal optical antireflection occurs when the effective complex refractive index of the composite film is zero.  相似文献   
39.
The oxime of 2-acetylcoumarone reacts with acetylene under pressure in the system KOH-DMSO unusually readily forming 2-(2-pyrrolyl)coumarone and the corresponding O-vinyl oxime. Under more rigid conditions 2-(1-vinyl-2-pyrrolyl)coumarone is formed. The possibility of a two-stage transformation of 2-acylcoumarones into 2-pyrrolylcoumarones has therefore been demonstrated for the first time.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 524–529, April, 2005.  相似文献   
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