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991.
Trace impurities (Ca, Cu, Fe, Mg, Mn, Na and Si) in 99.99% aluminum oxide were determined by inductively-coupled plasma atomic emission spectrometry (i.c.p./a.e.s.). The sample was fused with lithium carbonate/boric acid to determine Ca, Cu, Mg, Mn, Na and Si or dissolved in phosphoric/sulphuric acids to determine iron. Matrix effects on the calibration graphs for each element were studied: for accurate determinations, calibration solutions must contain lithium and boric acid (or aluminium and phosphoric and sulphuric acids for iron). 相似文献
992.
D. T. Clark M. Z. Abrahman 《Journal of polymer science. Part A, Polymer chemistry》1981,19(11):2689-2703
A systematic investigation has been made of the composition, gross structural features, and rates of deposition of plasma polymer films produced from the excitation of inductively coupled RF plasmas in the isomeric tetrafluorobenzenes. ESCA data reveal that the dominant reaction involves rearrangement such that under a wide variety of experimental conditions the composition of the crosslinked products remains essentially the same as that of the starting material. Small differences in rates of deposition are observed for the different isomers, and theoretical SCF MO studies at the MNDO level provides a basis for discussion of the experimental data. 相似文献
993.
Summary The relationship between R
M
and the concentration of the polar solvent in the moving phase was investigated for a number of aromatic nitro compounds
with additional polar groups (amino, methoxy, carbomethoxy, aldehyde). TLC data were correlated with analogous column chromatography
results. Linear R
M
(logk') vs. logX
S
relationships obtained for both techniques are interpreted in terms of a molecular model of adsorption. 相似文献
994.
D. T. Clark B. J. Cromarty A. Dilks 《Journal of polymer science. Part A, Polymer chemistry》1978,16(12):3173-3184
Nonempirical LCAO MO SCF computations (in the ΔSCF formalism) have been carried out of binding energies and relaxation energies for an extensive series of oxygen-containing organic systems encompassing most of the common functionalities. The molecules for which experimental data are available for comparison demonstrate the adequacy of the treatment for describing the relative binding energies for both the Cls and Ols core levels. A sound basis is therefore provided for the discussion of relative core binding energies (Cls and Ols) for functionalities for which experimental data are not available, that is, hydroperoxides, peroxides, peroxyacids, and peroxyesters, a knowledge of which is essential for investigations of the surface oxidation of polymers by means of ESCA. Cls shifts are discussed in terms of primary and secondary substituent effects of oxygen, which greatly simplify the analysis of complex unresolved spectra, whereas for the Ols levels a similar but less straightforward situation exists. The relaxation energies associated with both Cls and Ols core ionization follow a dependence on the binding energy for a given structural type. 相似文献
995.
996.
Summary Copper phthalocyanine tetrasulphonic acid has been found to work satisfactorily as an inside indicator in the cerimetric titration of hydro-quinone and metol. It has the advantage that the indicator correction in titrations with 0.01 N solutions of ceric sulphate is much less than with the ferroin indicator, amounting to only 0.02 ml for two drops of the indicator solution.Part II: See Z. analyt. Chem. 163, 1 (1958). 相似文献
997.
New combining rules are proposed for the well depth, ?, and interaction distance, σ, describing nonbonded interatomic forces for rare gas pair interactions. Concepts underlying current combining rules applied in simulations of macromolecular and polymer systems are shown to be incompatible with experimental data on the rare gases. The current combining rules are compared with the new results using the experimental data. Mathematical properties of combining rules are considered, and it is shown how to reduce combining rule formulas from a two-parameter to a single-parameter problem. It is also shown how to graphically analyze combining rules against experimental data. We demonstrate using this analysis technique that the rare gas potentials do not obey a single combining rule for the ? parameter but do follow a single combining rule for the σ parameter. Finally, we demonstrate that a combining rule using both ? and ω can be used to predict the ? parameters for the mixed rare gas pairs. © John Wiley & Sons, Inc. 相似文献
998.
S. M. Adekenov K. A. Aituganov K. M. Turdybekov S. V. Lindeman Yu. T. Struchkov 《Chemistry of Natural Compounds》1991,27(5):575-579
The new germacranolide argolide has been isolated from the epigeal part ofArtemisia glabella, and its structure has been shown by its conversion into oxopelenolide B. From the results of an x-ray investigation it is
suggested that argolide has the spatial structure of 3-oxo-4α,7α,6β(H)-germacra-1(10),11(13)-dien-6,12-olide.
Institute of Organic Synthesis and Coal Chemistry, Kazakh Academy of Sciences, Karaganda. A. N. Nesmeyanov Institute of Organometallic
Chemistry, Russian Academy of Sciences, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 653–657, September–October,
1991. 相似文献
999.
K. M. Turdybekov T. T. Edil'baeva V. A. Raldugin M. M. Shakirov A. T. Kulyyasov S. M. Adekenov 《Chemistry of Natural Compounds》1998,34(2):141-144
A new sesquiterpene lactone having the structure 3-acetoxy-1-hydroxy-6, 7(H)-germacra-4,10(14), 11(13)-trien-6, 12-olide has been isolated fromArtemisia subchrysolepis Filat. and has been called subchrysin. Its stereochemistry has been established by x-ray structural analysis.Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 176–180, March–April, 1998. 相似文献
1000.