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71.
J. Maier C. S. Kischkel M. Baumann 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1991,21(2):145-151
Using laser induced fluorescence spectroscopy the hyperfine structure of the even parity levels 4f 146s6d 3 D 1, 4f 14 6s8s 3 S 1 and 4f 13 5d6s6p (7/2, 5/2)J=1,2,3 as well as of the odd parity level 4f 14 6s6p 3 P 2 in neutral ytterbium has been investigated. The isotope shift of the transitions 4f 146s6p 3 P 0 → 4f 14 6s6p 3 D 1 and 4f 14 6s6p 3 P 2 → 4f 14 6s8s 3 S 1, 4f 13 5d6s6p (7/2, 5/2)J=1,2,3 could be measured with high accuracy. The results for the 4f 14 6s6p 3 D 1 level show a considerable influence of second order effects of the hyperfine interaction. The isotope shifts of the 4f 14 6s8s 3 S 1 and 4f 13 5d6s6p (7/2, 5/2)J=1 levels indicate a possible configuration mixing for these levels. 相似文献
72.
73.
P. E. Sulewski E. Bucher N. Stücheli C. S. Oglesby K. Friemelt M. Vögt J. R. Baumann Ch. Kloc 《Applied Physics A: Materials Science & Processing》1992,54(1):79-83
Recently, an anomalously large redshift of the absorption edge with electric field was claimed for -GaSe1–x
S
x
layered crystals. We have studied Bridgman grown -GaSe crystals as well as vapor transport grown -GaS, and 2H-WSe2. While we have observed a shift in the absorption edge for -GaSe similar to that reported in previous work, our results demonstrate that the redshift arises from Joule heating, and is thus temperature induced, rather than intrinsic. For -GaS, much larger resistivities virtually eliminate Joule heating, and our measurements of the electric field induced absorption edge shift yield an estimated upper limit of approximately 0.04 meV · cm/kV for a field of 2.4×103 kV/cm, in good agreement with the theoretical value expected for the Franz-Keldysh effect.Also at University of Konstanz 相似文献
74.
Klaus Baumann 《Communications in Mathematical Physics》1982,86(2):247-256
We extend a result about non-interacting fields given by Buchholz and Fredenhagen. Consider a massless, scalar field ø in 3 + 1 dimensional space-time which does not interact. The corresponding Hilbert space is assumed to be the FockspaceH of the free massless fieldA. This implies — as we show in the first part — that alln-point-functions are rational functions of their arguments. In the second part we use this fact to construct a symmetric, traceless tensorfield 1...n, relatively local to the original field ø, and connecting the vacuum with the one particle states. In the last part we prove 1...n to be relatively local to the free fieldA. 相似文献
75.
Normen Peulecke Andreas Ohff Wolfgang Baumann Rhett Kempe Vladimir V. Burlakov Uwe Rosenthal 《Journal of organometallic chemistry》1996,520(1-2):235-239
The reaction of Cp2Zr(L)(η2-Me3SiC2) (L = THF, py) with equimolar amounts of H2C = CMe-CHO at room temperature depends strongly on the ligands L and the solvents that are used. With L = THF, in the THF solution the insertion product 1 was isolated, whereas by conducting the reaction in n-hexane solution an alkyne substitution with 1,4-coordination of the methacrolein takes place and the binuclear complex [ 2 was obtained. In conttrast, with L = py (a stronger ligand) only a 1:1 ratio of 1 and 2 was observed in both THF and in n-hexane. At 50°C complex 1 was converted into 2 and the alkyne was eliminated quantitatively.
Complexes 1 and 2 were characterized by IR and NMR spectroscopical measurements and 1 by an additional X-ray structure determination. 相似文献
76.
Magdalena Kurdziel Elżbieta Szczepaniec-Cieciak Monika Watorczyk Barbara Dabrowska 《Journal of solution chemistry》2004,33(5):453-464
The solubility of solid 2-methyl-1,3-butadiene (isoprene) in liquid argon at a temperature of 87.3 K and in liquid nitrogen at 77.4 K has been measured by the filtration method. The hydrocarbon contents in solutions were determined using gas chromatography. GC–MS was used to identify impurities in the solute. The experimental value of the mole fraction solubility of solid isoprene in liquid argon at 87.3 K is (1.41 ± 0.27) × 10–6 and (1.56 ± 0.36) × 10–7 in liquid nitrogen at 77.4 K. The Preston–Prausnitz method was used for calculation of the solubilities of solid hydrocarbon in liquid argon in the temperature range 84.0–110.0 K and in liquid nitrogen from 64.0 to 90.0 K. The solvent–solute interaction parameters l
12 were also calculated. At 90.0 K liquid argon is a better solvent for isoprene than is liquid nitrogen. The experimental values of the solubilities of isoprene in liquid argon and nitrogen were compared with results obtained for selected unsaturated and aromatic hydrocarbons. 相似文献
77.
Strong cation-exchange chromatography (SCX-HPLC) was used in conjunction with inductively coupled plasma mass spectrometry (ICP-MS) to investigate cationic selenium species present in leaf extract of wild-type Brassica juncea supplemented with selenite. Total amount of Se accumulated by the leaves was found to be 352 microg g(-1). Cation-exchange solid-phase extraction (SCX-SPE) was used to pre-concentrate the cationic species present in the leaf extract. Methylselenomethionine (MeSeMet) and dimethylselenoniumproprionate (DMSeP) were synthesized and characterized by electrospray quadrupole time-of-flight MS (ESI-QTOF-MS). Laboratory synthesized and commercially available standards were used in chromatographic studies to identify the Se species in the leaf extract through retention time comparisons and standard addition method. Major cationic selenium species identified in the present study were MeSeMet and methylselenocysteine (MeSeCys) while selenomethionine (SeMet) was found in minor quantities. 相似文献
78.
Jörg Rethmeier Andreas Rabenstein Monika Langer Ulrich Fischer 《Journal of chromatography. A》1997,760(2):637-302
Depending on the sulfur species, picomoles of different inorganic sulfur compounds can be detected and separated by HPLC in one arrangement in a sample volume less than 50 μl. The combination of fluorescence labelling of reduced inorganic sulfur compounds such as sulfide (S2−), sulfite(SO32− and thiosulfate (S2O32−) with monobromobimane followed by an extraction of elemental sulfur (S°) by chloroform treatment enables the detection of all mentioned sulfur compounds as well as sulfate (remaining aqueous phase) in the same sample. While the derivatized sulfur compounds could be detected by their fluorescence emission at 480 nm, elemental sulfur is identified by its UV absorption at 263 nm. Sulfate in the remaining aqueous phase is detected by HPLC with indirect UV detection at 254 nm. Detection ranges for the different sulfur compounds examined are as follows: sulfide (5 μM to 1.5 mM), sulfite (5 μM to 1.0 mM), thiosulfate (1 μM to 1.5 mM), elemental sulfur (2 μM to 32 mM) and sulfate (5 μM to >1 mM). 相似文献
79.
Mendoza SM Whelan CM Jalkanen JP Zerbetto F Gatti FG Kay ER Leigh DA Lubomska M Rudolf P 《The Journal of chemical physics》2005,123(24):244708
Thin films of fumaramide [2]rotaxane, a mechanically interlocked molecule composed of a macrocycle and a thread in a "bead and thread" configuration, were prepared by vapor deposition on both Ag(111) and Au(111) substrates. X-ray photoelectron spectroscopy (XPS) and high-resolution electron-energy-loss spectroscopy were used to characterize monolayer and bulklike multilayer films. XPS determination of the relative amounts of carbon, nitrogen, and oxygen indicates that the molecule adsorbs intact. On both metal surfaces, molecules in the first adsorbed layer show an additional component in the C 1s XPS line attributed to chemisorption via amide groups. Molecular-dynamics simulation indicates that the molecule orients two of its eight phenyl rings, one from the macrocycle and one from the thread, in a parallel bonding geometry with respect to the metal surfaces, leaving three amide groups very close to the substrate. In the case of fumaramide [2]rotaxane adsorption on Au(111), the presence of certain out-of-plane phenyl ring and Au-O vibrational modes points to such bonding and a preferential molecular orientation. The theoretical and experimental results imply that the three-dimensional intermolecular configuration permits chemisorption at low coverage to be driven by interactions between the three amide functions of fumaramide [2]rotaxane and the Ag(111) or Au(111) surface. 相似文献
80.