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991.
海底沉积物的ICP-AES分析 总被引:1,自引:0,他引:1
海底沉积物用硝酸-高氯酸-氢氟酸消解,然后用ICP-AES法同时测定常量和微量元素。研究了样品中基体元素对微量元素测定的光谱干扰,并采用干扰曲线斜率法进行干扰校正,分析批量海底沉积物样品获得满意结果。 相似文献
992.
Long-range (3J) 13C-H coupling is a reliable probe to evaluate the stereochemistry of cycloaddition products. The method is best applied to carbonyl containing adducts but not restricted to them. Several structures have been revised and new ones evaluated. 相似文献
993.
994.
995.
Danielle Giron S. Monnier M. Mutz P. Piechon T. Buser F. Stowasser K. Schulze M. Bellus 《Journal of Thermal Analysis and Calorimetry》2007,89(3):729-743
Adequate very sensitive quantification methods are needed for the development and are also now required for the monitoring
of undesirable solid form(s) as routine tests. The pre-requisite for quantitation are selectivity, sensitivity and most important
the purity of standards and their proper storage, what is a challenge for metastable forms.
Several analytical techniques are available such as X-ray diffraction, spectroscopy, thermal analysis and microcalorimetry.
The different steps of the validation of the analytical methods and problems to be solved are discussed. Examples illustrate
the different techniques and compare their possible advantages and limits. The relative standard deviation of measurements
should allow for checking the homogenization procedure of mixtures for calibration. The validation should be carried out following
ICH guidelines for validation of analytical methods. Comparison of different techniques in adequate concentration range add
confidence in the analytical results. 相似文献
996.
Andrzej Czerwiński Iwona Kiersztyn Michał Grdeń 《Journal of Solid State Electrochemistry》2003,7(6):321-326
The effect of temperature on hydrogen and deuterium electrosorption into a palladium LVE (limited-volume electrode) has been
investigated. A decrease in hydrogen capacity (H/Pd ratio) with increasing temperature has been observed. Temperature strongly
influences the plots of measured H(D)/Pd values vs. potential scan rate. In addition, hydrogen absorption was found to be
dependent on the composition of the surrounding electrolyte solution. These results have confirmed the hypothesis that two
different mechanisms of hydrogen desorption from the palladium electrode take place, namely electrochemical oxidation and
non-electrochemical recombination. Further, the ratio between the rate constants for these two processes has been found to
change with temperature.
Electronic Publication 相似文献
997.
Summary The thermal behavior of KH2PO4, NaH2PO4 and Na2HPO4 under non-isothermal conditions using TG method with different heating rates was studied. The values of the reaction rate were processed by means of Friedmans differential-isoconversional method. A dependence of the activation energy vs. conversion was observed. Therefore a procedure based on the compensation effect (suggested by Budrugeac and Segal) was applied. A less speculative data processing protocol was offered by the non-parametric kinetics method suggested by Serra, Nomen and Sempere. Three steps were observed by non-isothermal heating: a dehydration, a dimerization and a polycondensation. The differences in the intimate reaction mechanism are determined by the initial number of water molecules. 相似文献
998.
Employing hot tungsten filament to thermal dissociate molecular hydrogen,we generated gas phase atomic hydrogen under ultra-high vacuum(UHV)conditions and investigated its interaction with Pt(111) surface.Thermal desorption spectroscopy(TDS)results demonstrate that adsorption of molecular hy- drogen on Pt(111)forms surface Had species whereas adsorption of atomic hydrogen forms not only surface Had species but also bulk Had species.Bulk Had species is more thermal-unstable than surface Had species on Pt(111),suggesting that bulk Had species is more energetic.This kind of weakly- adsorbed bulk Had species might be the active hydrogen species in the Pt-catalyzed hydrogenation reactions. 相似文献
999.
The complexes of rare earth picrate with N, N, N′, N′-tetraphenyl-3, 6-dioxaoctanediamide (TDD), [Eu(pic)3(TDD)]-2CH3CN and [Y(pic)3(TDD)], have been synthesized. The crystal structures reveal that TDD acts as a tetradentate ligand, forming a ring-like coordination
structure with its oxygen atoms together with one oxygen atom of the bidentate picrate. In the Eu (III) complex, the europium
ion with a larger ionic radius lies out of the ring, while in the Y (III) complex, the yttrium ion with a smaller ionic radius
enters the cavity of the ligand. The structures of the complexes are greatly affected by the ionic radii due to participation
of the picrates in coordination.
Project supported by the National Natural Science Foundation of China, the Doctoral Foundation of the State Education Commission
of China, and the Climb Plan Foundation of the State Science and Technology Commission of China. 相似文献
1000.
Ahmad Shaabani Abbas Rahmati Soheila Naderi 《Monatshefte für Chemie / Chemical Monthly》2007,138(6):553-557
Summary. Reaction of triphenylphosphine and an electron deficient acetylenic ester in the presence of strong N–H acid such as alkyl
and aryl sulfamides or acetamide produces phosphorous ylides at room temperature in CH2Cl2. The aryl sulfamide phosphoranes undergo a smooth transformation reaction in boiling toluene and produce iminophosphoranes. 相似文献