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1.
Solutions are presented herein of some contact problems connected with the torsion of a composite half-space. In the general case the problem of the torsion of a composite elastic half-space is examined by means of the rotation of a stiff finite cylinder welded into a vertical recess of this half-space. Moreover, the following particular problems on the torsion of such a half-space are considered.

1. 1) A composite half-space with a vertical elastic infinite core, twisted by means of the rotation of a stiff stamp affixed to the upper endplate of the elastic core.

2. 2) A half-space with a vertical cylindrical infinite hole, twisted by means of the rotation of a stiff finite cylinder welded into the upper part of this hole.

In the general case the solution of the problem reduces to the solution of an integral equation of the second kind on a half-line. The question of the solvability of this fundamental integral equation is investigated, and it is shown that its solution may be constructed by successive approximations.

Let us note that the problem of the torsion of a homogeneous half space and of an elastic layer by means of rotation of a stiff stamp has been considered by Rostovtsev [1], Reissner and Sagoci [2], Ufliand [3], Florence [4], Grilitskii [5] and others.

The problem of the torsion of a circular cylindrical rod and the half-space welded to it which are subject to a torque applied to the free endface of the rod has been considered by Grilitskii and Kizyma[6].

The torsion of an elastic half-space with a vertical cylindrical inclusion of some other material by the rotation of a stiff stamp on the surface of this half-space has been considered in [7], wherein it has been assumed that the stamp is symmetrically disposed relative to the axis of the inclusion and lies simultaneously on both materials.  相似文献   

2.
3.
The crystal structures of hydrate (1) and anhydrate (2) forms of 2,3-pentamethylene-3,4-dihydroquinazolin-4-one hydrochloride have been determined by X-ray structure analysis. Crystal data of 1 are 2(C13H14N2O)*3(HCl)*4.5 (H2O), triclinic P?1, Z=2, a=8.004(5), b=13.129(7), c=15.725(7) Å, α=106.45(4), β=92.61(4), γ=97.98(5), R=0.0652 and 2 are C13H14N2O*HCl, monoclinic C2/c, Z=8, a=21.360(4), b=5.954(1), c=21.263(4), β=117.89(3), R=0.0556. The crystal of the hydrate form 1is unstable. This form collapses easily with evaporation of H2O and part of HCl molecules from crystals. By recrystallizing destroyed form has been obtained stable crystal form 2.  相似文献   
4.
Fluorosilyl and Fluoroboryl Substituted Cyclotetrasilazanes. Synthesis and Crystal Structures Mono- and dilithiated octamethylcyclotetrasilazanes ( 1, 6 ) react with fluorosilanes and F2BN(SiMe3)2, respectively, under retention of the cyclotetrasilazane structure yielding the mono- and disubstituted compounds 2–5 and 7–13 . In the reaction of the dilithium compound 6 with a fluorsilane in equivalent amounts, the bicyclic compounds 14 and 15 are obtained. Crystallographic investigations of the compounds 2, 3, 8 , and 9 indicate that the monosilylated eight-membered ring has a cradle conformation while the disilylated ring has a chair conformation. The X-ray structure of the bicyclic system 14 indicates that the nitrogen atoms of the Si3N-units have a pyramidal environment.  相似文献   
5.
Bis(cyclodisilazane-1-yl) dimethylsilanes — Synthesis and Reactions The monolithium derivate of trisilazan-1-yl-cyclodisilazane 1 reacts with F3SiN (SiMe3)2 with substitution. The silyl-bridged cyclodisilazanes 3–6 are formed in the reaction of the dilithium derivate of 1 with fluoro- and chlorosilanes. Using lithiumamide and lithiummethanolate a controlled exchange of one fluoro atom of 4 occurs ( 7,8 ). 9 and 10 are formed by hydrolysis of 4 . The aminofunctional compounds 11 und 12 are obtained in the reaction of 5 and 6 with NH3. The dispirocyclus 13 is formed in the reaction of 8 with tert.-butyllithium. The reaction of dilithiated 1 with 4 gives the spirocyclus 14 . The crystal structure of 14 is discussed.  相似文献   
6.
Synthesis of Functional Carboxylic Acid Silylester Di-tert-butylsilandiol reacts with organic acid chlorides to chlorosilanoles R2Si(OH)Cl 1 (R = t-Bu). The phosphoric acid silylester 2 is obtained from 1 and POCl3. Lithiated halogenosilanoles react with carboxylic acid chlorides to give silylesters ( 3 – 7 ). Lithium (trimethyl-acetoxy)silanolate 8 is obtained in the reaction of the lithiated diol with the chloride of trimethylacetic acid. The analogous reaction with benzoyl chloride lead to the formation of the bis(benzoic acid) silylester 9 . The condensation product 10 is obtained in the reaktion of the lithiated aminosilanol (t-Bu)2Si(NH2)OLi with trimethylacetic acid chlorid and condensation of the formed ester with aminosilanol.  相似文献   
7.
We analytically investigate the effect of an external mirror on the stability of an injected semiconductor laser, the latter treated as injected damped oscillators. In the studied configuration, the injected semiconductor laser with an external mirror is under the influence of a chaotic oscillating optical signal that is generated by a similar semiconductor master laser. We derive our results in terms of the damping rate and resonance frequency. We show that the external mirror can eliminate the unstable modes of the injected laser at low frequencies. Furthermore, the mirror can enhance the damping of the oscillation modes of the injected semiconductor laser; consequently, the driven response of the injected laser may have a broad spectrum, even wider than that of the chaotic driving signal. We also show results for the bandwidths of the injection amplitude and phase increment as functions of the injection rate and feedback strength of the external mirror. In addition, we use bifurcation and time-series curves to describe the dynamical behavior of the injected laser. We identify the feedback strength of injected laser, relative to that of the master laser, which induces synchronization between the injected-laser oscillation modes and the master laser.  相似文献   
8.
The inclusion behaviour of a new water-soluble sulfonated calix[4]resorcinarene towards alkylammonium and N-methylpyridinium cations has been investigated on the basis of 1H NMR spectroscopy and pH-potentiometry data. The inclusion of the N-methylpyridinium cation has been found to be dependent on pH with the preferable inclusion of the methyl substituent in alkaline and the aromatic ring in neutral aqueous media.  相似文献   
9.
β-radiation detected nuclear magnetic resonance was applied to determine the location of 12B probe nuclei in a Ni3Al single crystal. Combining our results with those of channeling experiments it turned out that more than 90% of the 12B ions occupy the octahedral interstitial site with six Ni ions as nearest neighbours.  相似文献   
10.
P Raychaudhuri  C Mitra  K Dorr  KH Muller  G Kobernik  R Pinto 《Pramana》2002,58(5-6):1179-1182
Hole-doped rare-earth manganite La0.7Ca0.3MnO3 and the electron-doped manganite La0.7Ce0.3MnO3 both show a metal-insulator transition around 250 K associated with a ferromagnetic transition and colossal magnetoresistance. In an earlier publication we have reported the rectifying characteristic of La0.7Ca0.3MnO3/SrTiO3/La0.7Ce0.3MnO3 tunnel junction at room temperature, showing that it is possible to fabricate a diode out of the polaronic insulator regime of doped manganites. Here we report the magneto-transport properties of such a tunnel junction above and below the metal-insulator transition. We show, from the large positive magnetoresistance of the tunnel junction at low temperature, that La0.7Ce0.3MnO3 could be a minority spin carrier ferromagnet. The implication of this observation is discussed.  相似文献   
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