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71.
Ohne Zusammenfassung 相似文献
72.
If a vertex operator algebra satisfies , , then has a commutative (nonassociative) algebra structure called Griess algebra. One of the typical examples of commutative (nonassociative) algebras is a Jordan algebra. For example, the set of symmetric matrices of degree d becomes a Jordan algebra. On the other hand, in the theory of vertex operator algebras, central charges influence the properties of vertex operator algebras. In this paper, we construct vertex operator algebras with central charge c and its Griess algebra is isomorphic to for any complex number c and a positive integer d. 相似文献
73.
74.
Miyamoto K Kimura A Kuroda K Okuda T Shimada K Namatame H Taniguchi M Donath M 《Physical review letters》2012,108(6):066808
The surface of W(110) exhibits a Dirac-cone-like state with d character within a spin-orbit-induced symmetry gap. As a function of the wave vector parallel to the surface, it shows a nearly massless energy dispersion and a pronounced spin polarization, which is antisymmetric with respect to the Brillouin zone center. In addition, the observed constant energy contours are strongly anisotropic for all energies. This discovery opens new pathways to the study of surface spin-density waves arising from a strong Fermi surface nesting as well as d-electron-based topological properties. 相似文献
75.
Hatano M Ikeno T Miyamoto T Ishihara K 《Journal of the American Chemical Society》2005,127(31):10776-10777
A highly enantioselective cyanohydrin synthesis with aromatic aldehydes using chiral lithium binaphtholate aqua or alcohol complexes has been developed and is a simple and inexpensive catalyst suitable for process chemistry to give gram-scale cyanohydrins successfully. Dramatic improvements in enantiomeric excess have been realized along with an interesting changeover in absolute stereochemistry of cyanohydrin product against the thoroughly "dry" catalytic systems. 相似文献
76.
Yoshiaki Miyamoto Norihiro Wada Dr. Takahiro Soeta Dr. Shuhei Fujinami Prof. Dr. Katsuhiko Inomata Prof. Dr. Yutaka Ukaji 《化学:亚洲杂志》2013,8(4):824-831
The stereoselective direct transformation of N‐(propargylic)hydroxylamines into cis‐2‐acylaziridines was achieved by the combined use of AgBF4 and CuCl. Copper salts were found to promote the transformation of the intermediary 4‐isoxazolines into 2‐acylaziridines and both 3‐aryl‐ and 3‐alkyl‐substituted 2‐acylaziridines could be prepared by using this method. Furthermore, subsequent 1,3‐dipolar cycloaddition of azomethine ylides that were generated in situ from the intermediary 2‐acylaziridines with maleimides was achieved in a stereoselective one‐pot procedure to afford the corresponding 2‐acylpyrrolidines, which consisted of an octahydropyrrolo[3,4‐c]pyrrole skeleton. 相似文献
77.
78.
K. Yanagisawa H. Takeda K. Miyamoto S. Fuma N. Ishii 《Journal of Radioanalytical and Nuclear Chemistry》2002,251(2):277-280
Tracer experiments on the transfer of carbon from culture solution to Daphnia magna through phytoplankton have been carried out using 13C and infrared absorption method. The purpose of this experiment is to investigate the experimental systems for the use of 13C in aquatic system. Daphnia magna was cultured in a 100 ml of solution containing phytoplankton and 20 mg of NaH13CO3 for 24 hours in the light and dark conditions (2000 lux, 14 hour light and 10 hours dark at 25 C). The concentration of 13C in Daphnia magna under light condition was about 2.0% (atom% excess), while in the dark condition 13C tracer was not detected. The concentration of 13C in phytoplankton under light condition was around 20%. It was suggested that 13C added as carbonate in the culture solution was photosynthetically assimilated by phytoplankton and then transferred to Daphnia magna. Using this system, the effect of UV-B exposure on the 13C uptake of Daphnia magna has been examined. The UV-B intensity was 95 mW/cm2 and exposure time was 15, 30, and 60 minutes. The concentration of 13C in Daphnia magna decreased with increasing exposure time. The Daphnia magna exposed to UV-B for 15 minutes intakes phytoplankton as much as control, while 30 minutes and 60 minutes exposures were lower than control. The lower concentrations of 13C observed in Daphnia magna were due to less intake of phytoplankton caused by the UV-B exposure. 相似文献
79.
Takenaka S Susuki N Miyamoto H Tanabe E Matsune H Kishida M 《Chemical communications (Cambridge, England)》2010,46(47):8950-8952
Pd cathode catalysts for polymer electrolyte fuel cells have been covered with silica layers a few nanometres thick. The silica-coated Pd catalysts showed high activity and excellent durability for the oxygen reduction under the severe cathode conditions of PEFCs, while Pd catalysts without silica-coating were seriously deactivated under the same conditions. The coverage of Pd metal with silica prevents the diffusion of Pd species out of the silica layers. 相似文献
80.
Nishiura M Hou Z Wakatsuki Y Yamaki T Miyamoto T 《Journal of the American Chemical Society》2003,125(5):1184-1185
Various terminal alkynes have been cleanly dimerized into the corresponding head-to-head (Z)-enynes by use of the half-metallocene lutetium alkyl complexes Me2Si(C5Me4)(NAr)Lu(CH2SiMe3)(THF) (Ar = Ph, C6H3Me2-2,6, C6H2Me3-2,4,6) as catalysts. Aromatic C-Cl, C-Br, and C-I bonds, which are known to be extremely susceptible to reductive cleavage by transition metals, survived in the present reactions. The corresponding dimeric alkynide species [Me2Si(C5Me4)(NAr)Lu(mu-CCR)]2 are thought to be the true catalysts, some of which have been isolated and structurally characterized. These alkynide species were thermally stable and soluble at the reaction temperatures (80-110 degrees C), but they precipitated upon cooling to room temperature after completion of the reaction. Therefore, this catalyst system works homogeneously but can be separated and reused, thus constituting the first example of a recyclable catalyst system for the dimerization of terminal alkynes and also the first example of (Z)-selective head-to-head dimerization of aromatic terminal alkynes. 相似文献