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1.
O. A. Alekseeva N. I. Sorokina I. A. Verin T. Yu. Losevskaya V. I. Voronkova V. K. Yanovskii V. I. Simonov 《Crystallography Reports》2003,48(2):205-211
This study is a continuation of research into the atomic structure and physical properties of niobium-doped potassium titanyl phosphate crystals, KTiOPO4 (KTP: Nb). Crystals containing 7 and 11 at. % of niobium were grown and studied. With an increase in niobium content, the number of vacancies and additional potassium positions in the structure also increase. This fact accounts for an increase in both the intensities of relaxation peaks and the conductivity of KTP: Nb crystals. 相似文献
2.
Girard V Farrenq R Sorokin E Sorokina IT Guelachvili G Picqué N 《Chemical physics letters》2006,419(4-6):584-588
The spectral dynamics of a mid-infrared multimode Cr(2+):ZnSe laser located in a vacuum sealed chamber containing acetylene at low pressure is analyzed by a stepping-mode high-resolution time-resolved Fourier transform interferometer. Doppler-limited absorption spectra of C(2)H(2) in natural isotopic abundance are recorded around 4000 cm(-1) with kilometric absorption path lengths and sensitivities better than 3 10(-8) cm(-1). Two cold bands are newly identified and assigned to the ν(1)+ν(4) (1) and ν(3)+ν(5) (1) transitions of (12)C(13)CH(2). The ν(1)+ν(5) (1) band of (12)C(2)HD and fourteen (12)C(2)H(2) bands are observed, among which for the first time ν(2)+2ν(4) (2)+ν(5) (-1). 相似文献
3.
Starting with a partition of a rectangular box into subboxes, it is shown how to construct a natural tetrahedral (type-4) partition and associated trivariate C 1 quintic polynomial spline spaces with a variety of useful properties, including stable local bases and full approximation power. It is also shown how the spaces can be used to solve certain Hermite and Lagrange interpolation problems. 相似文献
4.
V. I. Voronkova I. N. Leont’eva N. I. Sorokina T. I. Ovsetsina I. A. Verin 《Crystallography Reports》2006,51(6):977-981
A series of iron-doped KTiOPO4 (KTP: Fe) single crystals in which iron substitutes for 0.1–0.3% titanium was grown. The structure of the KTP: Fe crystals was determined, and their dielectric and conducting properties were studied. An X-ray diffraction analysis failed to reveal such asmall amount of Fe+3 ions in titanium octahedral positions of the structure. It was found that an increase in the iron concentration results in a lowering of the symmetry of Ti(1)O6 and Ti(2)O6 octahedra. The splitting of the dielectric anomaly due to the ferroelectric phase transition was explained by the mechanism of incorporation of an impurity into different growth pyramids of the crystals. It was established that the aging of the KTP: Fe crystals leads to changes in the permittivity and electrical conductivity during long storage. 相似文献
5.
S. A. Lebedev V. S. Lopatina R. S. Sorokina S. S. Berestova E. S. Petrov I. P. Beletskaya 《Russian Chemical Bulletin》1987,36(11):2329-2332
Conclusions Condensation of aryl bromides with styrenes in acetonitrile in the presence of nickel organometallic complex catalysts and metallic zinc occurs regio- and stereoselectively to give E-stilbenes.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2508–2511, November, 1987. 相似文献
6.
V. G. Berezkin E. Yu. Sorokina A. I. Sokolov B. A. Rudenko 《Journal of Analytical Chemistry》2003,58(1):61-67
The effects of the presence of water vapor in the carrier gas and the temperature on the retention of achiral and chiral compounds, enantioselectivity, and performance of an open-tubular column with a cyclodextrin-containing phase were studied. The use of a carrier gas containing water vapor in the determination of optically active isomers, such as camphor, slightly increases the retention factor. A substantial improvement of performance characteristics of the column was found: for hydroxy compounds, the column performance increased by two to three times and the peak symmetry improved by more than twice. 相似文献
7.
A. M. Makarevich P. R. Abdyushev N. M. Sorokina I. E. Korsakov N. P. Kuz’mina 《Russian Journal of Coordination Chemistry》2006,32(10):707-711
A reaction of samarium oxide, nickel oxocarbonate, and diethylenetriaminepentaacetic acid (H5DTPA) taken in stoichiometric proportions in water gave SmNiDTPA · 10H2O as a glassy solid. The formation of this heterometallic complex was confirmed by data from elemental analysis, IR spectroscopy, thermal analysis, and X-ray fluorescence analysis. An aqueous solution of the complex was used to deposit SmNiO3 films onto a single-crystal SrTiO3(001) substrate. The SmNiO3 phase in films obtained upon 3-h annealing at 500°C was identified by powder X-ray diffraction. Films deposited from a solution of an equimolar mixture of monometallic samarium and nickel diethylenetriaminepentaacetates contained no samarium nickelate. 相似文献
8.
The regularities of vapor-phase nitration of cellulose with HNO3 under conditions of natural convection and hindered heat removal in the absence of air were studied using the nonisothermal kinetic method. It was established that the nitration rate at the depth of conversion of 0.08 to 0.7 is described by the kinetic law d/dt =k
1
p/(1+), wherek
1 = 104.49±0.6 exp(–A/RT) s–1 atm–1, = 10–35.5±15.7exp(B/RT),A = 36.6±3.8 kl mol–1, andB = 203±88 kJ mol–1. The diffusion mechanism of vapor-phase nitration of cellulose, which explains the high value of activation energies, is discussed. The effective diffusion coefficient of HNO3 in cellulose at 25 °3.7 · 10–7 cm2 s–1) and the activation energy of diffusion (38.3±4.2 kJ mol–1) were estimated.For Part 1, see Ref. l.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1981–1985, August, 1996. 相似文献
9.
A. N. Grinev A. A. Druzhinina I. K. Sorokina 《Chemistry of Heterocyclic Compounds》1976,12(9):1048-1050
1-Ethoxycarbonyl-3-phenyl- and 3-phenylpyrazino[1,2-a]benzimidazoles were synthesized by reaction of 2-ethoxalyl- and 2-diethoxymethyl-N-phenacylbenzimidazoles, obtained from the corresponding sodium derivatives of benzimidazole and phenacyl bromide, with ammonium acetate.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1266–1267, September, 1976. 相似文献
10.
V.?S.?Leshinlevasi@highp.chem.msu.ru" title="levasi@yandex.ru levasi@highp.chem.msu.ru" itemprop="email" data-track="click" data-track-action="Email author" data-track-label="">Email author N.?E.?Sorokina V.?V.?Avdeev 《Russian Journal of Electrochemistry》2005,41(5):572-575
Anodic oxidation of highly oriented pyrolytic graphite in an electrolyte containing concentrated sulfuric and anhydrous phosphoric acids is studied for the first time. The synthesis was carried out under galvanostatic conditions at a current I = 0.5 mA and an elevated temperature (t = 80°C). Intercalation compounds of graphite (ICG) are shown to form at all concentration ratios of H2SO4 and H3PO4 acids. The intercalation compound of step I forms in solutions containing more than 80 wt % H2SO4, a mixture of compounds of intercalation steps I and II forms in 60% H2SO4, intercalation step II is realized in the sulfuric acid concentration range from 10 to 40%, and a mixture of compounds of intercalation steps III and II is formed in 5% H2SO4 solutions. The threshold concentration of H2SO4 intercalation is ∼2%. With the decrease in active intercalate (H2SO4) concentration, the charging curves are gradually smoothed, the intercalation step number increases, and the potentials of ICG formation also increase. As the sulfuric acid concentration in the electrolyte changes from 96 to 40 wt %, the filled-layer thickness d
i in ICG monotonously increases from 0.803 to 0.820 nm, which apparently is associated with the greater size of phosphoric acid molecules. With further increase in H3PO4 concentration in solution, d
i remains unchanged. According to the results of chemical analysis, both acids are simultaneously incorporated into the graphite interplanar spacing and their ratio in ICG is determined by the electrolyte composition.__________Translated from Elektrokhimiya, Vol. 41, No. 5, 2005, pp. 651–655.Original Russian Text Copyright © 2005 by Leshin, Sorokina, Avdeev. 相似文献