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排序方式: 共有502条查询结果,搜索用时 15 毫秒
1.
2.
Periodica Mathematica Hungarica - As it is well-known a Minkowski space is a finite dimensional real vector space equipped with a Minkowski functional F. If the square of the Minkowski functional... 相似文献
3.
We prove that a finite solvable group G has at least (49p+1)/60 conjugacy classes whenever p is a prime such that p2 divides the order of G. We also construct an infinite family of finite solvable groups, where this bound is attained. 相似文献
4.
I. Vincze 《Journal of Mathematical Sciences》1997,84(3):1190-1196
After establishing the formula of information, we turn to two cases: to the independent case and to the dependent case. If
the characteristics of the particles (e.g., the energy) as random variables are independent, we come in the discrete case
to the Boltzmann distribution, while in the continuous case we come to the Gibbs formula-irrespectively of whether the particles
are distinguishable or not. Our effort is nimed at clarity of the ideas, not at their mathematical completeness.
Supported by the Hungarian National Foundation for Scientific Research (grant No. T 016384 and No. 4007-016237)
Proceedings of the XVII Seminar on Stability Problems for Stochastic Models, Kazan, Russian, 1995, Part III. 相似文献
5.
D. Kaptás T. Kemény J. Balogh L. F. Kiss L. Gránásy I. Vincze 《Hyperfine Interactions》1994,94(1):1861-1865
The temperature dependence of the iron hyperfine field distribution is reported in melt-quenched amorphous Fe-Zr alloys. The most remarkable feature is the compositinal change in the shape of the average hyperfine field versus temperature curves. The unusual increase in the average hyperfine field below about 85 K is a characteristic feature of the RSG systems; however, no anomaly is observed in the width of the hyperfine field distribution as a function of temperature. The results cannot be properly explained in the framework of the existing spin glass models. 相似文献
6.
J. Balogh D. Kaptás L. F. Kiss T. Kemény L. Bujdosó I. Vincze 《Hyperfine Interactions》2006,169(1-3):1343-1347
Magnetic multilayers of 57Fe with nominal thickness, T
nom, between 0.4 and 1.0 nm separated by 3.0 nm Al spacer layers were prepared by alternate deposition of the constituents in
high vacuum. The samples were investigated at 4.2 K in external magnetic field. A fraction of Fe atoms corresponding to about
0.3 nm equivalent Fe-thickness was found to mix into the Al spacer. The extremely strong magnetic anisotropy observed for
T
nom < 0.8 nm is attributed to Fe layers of approximately two atomic planes thick. The anisotropy decreases considerably after
the building up of the third Fe atomic layer starts at T
nom = 0.8 nm, but full saturation was not achieved even for T
nom = 1 nm and 3 T magnetic field applied perpendicularly to the sample plane. 相似文献
7.
Pierre Laszlo 《Angewandte Chemie (International ed. in English)》1978,17(4):254-266
With the availability of Fourier transform spectrometers, 23Na-NMR spectroscopy has become an important tool. It affords direct insight into solvation and ion pairing phenomena, both in organic and in bio-inorganic systems. Monitoring the chemical shifts and linewidths of 23Na signals gives access to binding constants, reorientational correlation times and the microdynamics of the sodium coordination shell. The binding of other cations can also be studied by 23Na-NMR spectroscopy, in competition experiments. 相似文献
8.
Stevens SM Chung AY Chow MC McClung SH Strachan CN Harmon AC Denslow ND Prokai L 《Rapid communications in mass spectrometry : RCM》2005,19(15):2157-2162
A fluorescent affinity tag (FAT) was synthesized and was utilized to selectively modify phosphorylated serine and threonine residues via beta-elimination and Michael addition chemistries in a 'one-step' reaction. This labeling technique was used for covalent modification of both phosphoproteins and phosphopeptides, allowing identification of these molecular species by fluorescence imaging after solution- or gel-based separation methods. In addition to the strong fluorescence of the rhodamine tag, a commercially available antibody can be used to enrich low-abundance post-labeled phosphopeptides present in complex mixtures. Application of this methodology to phosphorylation-site mapping has been evaluated for a phosphoprotein standard, bovine beta-casein. Initial results demonstrated low femtomole detection limits after fluorescence image analysis of FAT-labeled proteins or peptides. 相似文献
9.
Crowe MC Kapoor RN Cervantes-Lee F Párkányí L Schulte L Pannell KH Brodbelt JS 《Inorganic chemistry》2005,44(18):6415-6424
Electrospray ionization (ESI) quadrupole ion trap mass spectrometry (QIT-MS) and collisionally activated dissociation (CAD) were used to evaluate the rare-earth binding properties of two hydrophobic carbamoylmethylphosphine oxide (CMPO) ligands, the normal bidentate variety, (t-BuC6H4)2P(O)CH2C(O)N(i-Bu)2 (A), a new potentially tridentate extractant, (t-BuC6H4)2P(O)CH[CH2C(O)N(i-Bu)2]C(O)N(i-Bu)2 (B), and tributyl phosphate. The mass spectral results obtained from analysis of 1% HNO3/methanol solution containing the ligands and dissolved lanthanide salts reveal that the favorable stoichiometries of the ligand/metal/nitrate complexes are 2:1:2 for the bidentate ligand A, 1:1:2 for the tridentate ligand B, and 3:1:2 for the monodentate tributyl phosphate. These observed stoichiometries correlate with the number of available binding sites on each ligand as well as with potential steric effects. Energy-variable collisionally activated dissociation experiments showed that for the 2:1:2 complexes involving ligand A or B, as the ionic radius of the bound metal decreased, the removal of nitric acid required less energy and resulted in less extensive spontaneous solvent coordination. This experimental trend suggests that, as the ionic radius of the lanthanide ion decreases, a pair of the carbamoylmethylphosphine ligands is able to more completely solvate the bound metal ion thereby weakening the nitrate-metal interaction. 相似文献
10.
Stphane Chalais Andr Cornlis Andr Gerstmans Wacaw Koodziejski Pierre Laszlo Arthur Mathy Pierre Mtra 《Helvetica chimica acta》1985,68(5):1196-1203
Multiple chlorinations and arylations at the tertiary positions of adamantane are promoted by FeCl3-doped K10 montmorillonite in CCl4 or in aromatic solvents. The process, remarkably easy to implement, can be tailored to selective formation of monosubstituted 1-adamantyl derivatives or 1,3-disubstituted adamantanes. The process achieves alkylation at the meta- and para-positions of toluene leading to a purely statistical distribution and displays no substrate specificity in competition experiments between toluene and benzene. 相似文献