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41.
A model of soliton ion mobility in one-dimensional incommensurate structures is considered as the possible mechanism of information transmission in molecular systems. Numerical calculations of the dependence of the diffusion activation energy on the concentration of mobile ions are performed. Experimental NMR data on lithium ion mobility in a model LixNbSe3 (0Zhurnal Strukturnoi Khimii, Vol. 34, No. 6, pp. 135–140, November–December, 1993.Translated by L. Chernomorskaya 相似文献
42.
L. D. Asnin A. A. Fedorov Yu. S. Chekryshkin 《Russian Journal of Applied Chemistry》2007,80(2):263-267
Frontal chromatography was used to study the adsorption dynamics and adsorption equilibrium of chlorobenzene on a 5% V2O5/Al2O3 catalyst at temperatures of 50 and 100°C. The mixed-diffusion model was employed to describe the elution curve and evaluate the effective coefficients of external mass exchange and diffusion within transport pores. 相似文献
43.
L. Ya. Zakharova S. B. Fedorov L. A. Kudryavtseva V. A. Bel'skii A. B. Mirgorodskaya B. E. Ivanov 《Russian Chemical Bulletin》1990,39(8):1555-1559
The hydrolysis of bis(chloromethyl)phosphonic acid p-nitroanilide has been studied in the pH range 6.86–13.0 and the effects of ionic surfactant micelles on this process have also been examined. The nature of the micellar effects of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfate (SDS) on this reaction lead us to conclude that both the neutral and anionic forms of the substrate are reactive, and that in the range of pH > pKa hydrolysis of the ionic form of the anilide predominates, while at pH < pKa the reaction of the neutral form is predominant. The binding constants for both the neutral and anionic forms of bis(chloromethyl)phosphonic acid p-nitroanilide in micellar CTAB and SDS solutions have been determined using a kinetic method, as well as by measuring the changes in the acid-base properties of the substrate resulting from the influence of micelles.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1718–1722, August, 1990. 相似文献
44.
V. I. Dostovalova L. A. Fedorov Y. Knuutinen E. Kolehmainen J. Paasivirta 《Russian Chemical Bulletin》1994,43(4):566-573
A two-particle system of OY-Cl and OY-Br mixed increments for predicting13C NMR chemical shifts of polyhalogenated polyoxybenzenes has been developed. It has been found that only theortho- and para-interactions of the OY and Hal substituents contribute significantly to the13C chemical shifts and that theortho-effects of the OY located between Ha1 and H and those of the OY located between two Ha1 atoms are different. Additional effects are due to solvating solvents. The increment scheme is predictive over the whole class of compounds under consideration and may be realized on personal computers.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 617–624, April, 1994. 相似文献
45.
A new topological approach to predicting the13C NMR chemical shifts of polysubstituted benzenes has been proposed (in the example case of compounds with substituents of one kind of the type C6H6–nXn). The collective interactions of several substituents X [X=CH3, C2H5, iso-C3H7, CF3, COOH, f, Cl, Br, Si(CH3)3] have been expressed in the framework of a regression treatment in terms of two-particle increments. The chemical shift of each carbon atom has been represented in the form of an equation containing 17 parameters. The calculation scheme can be transformed and expanded for use even in the calculation of the spectra of compounds not previously studied. The calculated shifts for some previously investigated compounds and some compounds not previously investigated have been presented. The error in reproducing chemical shifts is equal to 0.2–0.3 ppm (and may be as high as 0.8 ppm for only a few measurements).V. I. Vernadskii Institute of Geochemistry and Analytical Chemistry, Academy of Sciences of the USSR. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 2, pp. 62–71, March–April, 1991. 相似文献
46.
E. D. Khairitdinova E. M. Tsyrlina L. V. Spirikhin N. I. Fedorov M. S. Yunusov 《Chemistry of Natural Compounds》2005,41(5):575-577
The known alkaloids deltaline, methyllycaconitine, elasine, and the new norditerpene alkaloid alpinine were isolated from
the aerial part of Delphinium alpinum. The structure of the last was proposed as 1α,6β, 16β-trimethoxy-7-hydroxy-8-ethoxy-14α-propionyloxy-4β-(2″-methyl)succinylanthranoyloxymethyl-N-ethylaconitane
on the basis of PMR, 13C NMR, IR, and mass spectra.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 469–471, September–October, 2005. 相似文献
47.
Yu. V. Mironov S. F. Solodovnikov V. E. Fedorov Yu. V. Gatilov 《Journal of Structural Chemistry》2004,45(5):874-878
The reaction of a water solution of K4Re6Te8(CN)6 with a solution of Mn(NO3)2 in 0.02M hydrochloric acid in the presence of DMF gave crystals of a cluster rhenium complex [{ Mn(H2O)2(DMF)}2Re6Te8(CN)6]·2H2O. The structure of the compound was determined by single crystal X-ray diffraction (a = 12.6679(9) Å, b = 17.4524(12) Å, c = 9.7882(6) Å, β = 105.570(6)°, V = 2084.6(3) Å3, Z = 2, space group P21/n, R = 0. 0389). In the complex, the [Re6Te8(CN)6]4− cluster anions are linked to Mn2+ cations by the cyanide bridges, the manganese cations being additionally coordinated by the DMF molecule and two water molecules. The neighboring clusters are joined by Re-C-N-Mn bridges into a three-dimensional framework possessing cavities filled with doubly disordered water molecules.Original Russian Text Copyright © 2004 by Yu. V. Mironov, S. F. Solodovnikov, V. E. Fedorov, and Yu. V. Gatilov__________Translated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 5, pp. 918–922, September–October, 2004. 相似文献
48.
L. P. Kozeeva M. Yu. Kameneva N. V. Podberezskaya I. G. Vasilieva N. V. Kuratieva D. Yu. Naumov V. A. Nadolinnyi V. E. Fedorov 《Journal of Structural Chemistry》2004,45(2):253-261
Cooling a melt of a Bi–Sr–Ca–Cu–O system (Bi:Sr:Ca:Cu = 4:3:3:4 or 2:2:2:4) from 1000°C-1050°C yielded crystals of a new red-colored nonsuperconducting phase, accompanying the superconducting 2212 and 2201 phases. Based on the EPR spectra, it was concluded that copper is univalent in this compound. The new phase has a composition Bi2.2Sr1.6Ca1.3Cu2Ox. The X-ray diffraction pattern has been indexed, and the unit cell parameters of the phase have been determined: space group P2/m, a = 12.93, b = 4.55, c = 10.94 ; = 102.72°. 相似文献
49.
The charged particle scattering in the presence of a regular magnetic field is considered starting from the Boltzmann kinetic equation in the case of an arbitrary relation between the mean free path and the distance from a particle source. It is shown that the Green function for the kinetic equation can be represented as the sum of the distribution functions of non-scattered particles which propagate with the injection pitch angle and of the scattered ones. The obtained Green function of the Boltzmann equation and also the particle density describe the space-time-pitch angle cosmic ray distribution that corresponds to an instantaneous particle injection at a particular pitch angle.This work was supported by International Science Foundation (grant N UC 8000) and by Slovak Grant Agency for Science (grant No. 1353/95). 相似文献
50.
A. V. Virovets N. V. Podberezskaya M. N. Sokolov I. V. Korobkov V. P. Fedin V. E. Fedorov 《Journal of Structural Chemistry》1993,34(2):292-295
The crystal structure was determined for Nb2S4(S2NCEt2)4 obtained in 48% yield by the reaction of Cs4Nb2S4(NCS)8 with NaS2CNEt2 in water: a=21.181(8), b=6.958(1), c=16.623(6) Å, =133.95(2)o, V = 1764(1) Å3, space group C2/m, Z=2, dcalc=1.708 g/cm3. The measurements were carried out on a Syntex P21 diffractometer with CuK radiation. A total of 2536 reflections were measured, of which 990 were used, Raniso=0.0444. The basic fragment in this molecule is [Nb2(2–S2)2]4+, the Nb–Nb distance in which corresponds to a metal-metal single bond. The molecule is partially disordered over two positions about the twofold axis and mirror plane of the C2/m space group. The dithiocarbamate and disulfide ligands with bidentate coordination form a distorted square antiprism about each of the niobium atoms as in NbS2Cl2. The anomalously large S–S bond length in the S2 ligand [2.282(5) Å] may be attributed to inaccuracy in the determination due to disorder.Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 34, No. 2, pp. 134–138, March–April, 1993. 相似文献