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991.
M. R. Corson B. Kolk G. Hoy G. O. Zimmerman A. M. van der Kraan P. C. M. Gubbens 《Hyperfine Interactions》1978,4(1-2):411-414
A3He-4He dilution refrigerator was constructed to perform Mössbauer measurements well below 4.2K. Results are reported here on the pseudobinary Laves-Phase system Y (Fe1-x Cox)2 for x=0.978. We found that at low temperatures, the Fe ions undergo a disordered magnetic phase transition, with a Curie temperature of approximately 4K and a saturation field of 96K0e. The easy axis of magnetization appears to be the [111] direction. This study is an extension to very low temperatures of previous work on the system with 0X0.978.Supported by the NSF Grant No. DMR 73-07665 AO 3 相似文献
992.
Two regions of frequency dispersion of capacitance and conductivity have been discovered in the semiconducting glass ceramics BaTiO3 and KNbO3 which have a positive temperature resistance coefficient (PTRC). The low-frequency region (102–103 Hz) of dispersion is associated with the existence of barrier layers at the electrodes and the high-frequency region (beginning in the region 105–106 Hz), with the existence of barrier layers at grain boundaries. The frequencies fm at which maxima of tan corresponding to both dispersion regions diminish in the temperature range of PTRC whereas in the higher region of PTRC they again increase with a rise in temperature. The anomalous temperature dependence of fm is explained on the basis of the assumption that charge carriers in the barrier layers act as relaxation oscillators and the variations in the barrier heights are described by the Heywang model.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 9, pp. 76–81, September, 1978. 相似文献
993.
The determination of nine rare earth elements in rock samples by epithermal neutron activation, followed by a simple group-separation procedure and Ge(Li) γ-ray spectrometry, is described. This method is found to be advantageous for the determination of Nd, Gd, Ho, Er and Lu by means of the short-lived nuclides149Nd,159Gd,166Ho,171Er and176m Lu. Precision for La, Sm and Eu is similar to that of thermal neutron activation, that for Dy is worse. Samples of the standard rocks, basalt BCR-1 and granite G-2, were analyzed by this procedure and the results obtained are compared with previously reported data. 相似文献
994.
Ya. S. Kayukov P. M. Lukin O. E. Nasakin V. N. Khrustalev V. N. Nesterov M. Yu. Antipin V. V. Sheverdov 《Chemistry of Heterocyclic Compounds》1997,33(4):423-425
It has been established by x-ray structural analysis that on reacting 4-oxoalkane-1,1,2,2-tetracarbonitriles with aldehydes
6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles are formed and not 3-imino-2,6-dioxabicyclo[2,2,2] octane-4,8,8-tricarbonitriles
as has been proposed.
Chuvash State University, Cheboksary 428015. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 497–499,
April, 1997. 相似文献
995.
996.
The infrared spectra in the OH-stretching and HOH-bending regions of H2O, and in the OH-stretching region of HDO dissolved in a number of ketones and ethers have been recorded. The number of component bands and their wavenumbers, halfwidths and intensities, as well as the total OH-stretching intensity in each solvent, have been interpreted in terms of a model for the types of hydrogen bonded solvent:water complexes formed in these systems.The effect of temperature on the spectra of H2O in some of the ketones has been rationalized on the basis of the equilibrium existing between the different hydrogen bonded species present in solution. 相似文献
997.
A chelate-forming ion exchanger, iminodiacetic acid/ethylcellulose, is used for the separation of trace metals from waters and different organic solvents. Added uranium was collected from sea waters with recoveries of about 97%. Graphite-furnace atomic absorption spectrometry and solution spectrophotometry were used to quantify the metals. For the direct determination of trace metals in waters by the graphite-furnace method, a simple matrix-matching method is described. The detection limit for cadmium was 0.1 μg l?1 and for lead 1 μg?1 in drinking water. 相似文献
998.
I. A. Litvinov O. N. Kataeva V. A. Naumov R. P. Arshinova B. A. Arbuzov 《Russian Chemical Bulletin》1989,38(1):63-66
Conclusions X-ray structure analysis shows that for 4,5;7,8(4,4 -dimethyl-6,6-di-tert-butyl)-dibenzo-6H-2-diethylamino-2-thiono-1,3,2-dioxaphosphocine, the boat-chair conformation of Cs symmetry with an equatorial diethylamino group occurs in the crystal.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 74–77, January, 1989. 相似文献
999.
Charles O. Okafor 《Journal of heterocyclic chemistry》1976,13(1):107-110
The reactions of 2-amino-3-hydroxypyridine and 2-chloro-3-nitropyridine in various solvents and in the presence of certain catalysts were studied. A dilute acid-catalysed procedure led to a 45% yield of 3-hydroxy-3-nitro-2,2-dipyridylamine which was also obtained by refluxing in alcoholic potassium hydroxide for several hours. The diarylamine was converted to 1,9-diazaphenoxazine by base-catalysed intramolecular condensation in refluxing DMSO. The same diazaphenoxazine was obtained directly by prolonged base-catalysed reaction of the starting pyridine compounds in DMSO. From a study of the infrared spectrum of the diarylamine precursor, it was found that strong NHO hydrogen bonding is responsible for the failure of the cyclization step in either aqueous or alcoholic base. This problem was overcome by the use of DMSO as the reaction solvent. Structural assignments were made by a study of their ultraviolet, infrared, nmr and mass spectra and the mechanistic pathways were also discussed. 相似文献
1000.
O. B. Ryabova E. Yu. Khmel’nitskaya V. A. Makarov L. M. Alekseeva N. B. Grigor’ev V. G. Granik 《Russian Chemical Bulletin》2005,54(12):2873-2879
On heating at pH 6.86, 4-(N,N-dialkylthiocarbamoylthio)-5-nitropyrimidines are transformed into dithiolopyrimidines, which are either oxidized to bis(4-dialkylthiocarbamoylpyrimidin-5-yl)
disulfides or converted into 4,6-diamino-5-nitropyrimidine derivatives with carbon disulfide elimination. The direction of
the reaction is determined by the nature of a substituent in position 2 of pyrimidine and the bulk of the thiocarbamate substituent.
Mechanistic schemes for these processes were proposed.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2777–2783, December, 2005. 相似文献