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51.
52.
Poly(2,5-dimethoxy-1,4-phenylene) was prepared by oxidative polymerization of p-dimethoxybenzene with aluminum chloride and copper(II) chloride in nitrobenzene under reduced pressure. The polymers obtained were soluble in sulfuric acid and fusible at 320°C. The intrinsic viscosity of the polymer was ca. 0.07 in sulfuric acid. Demethylation of methoxy groups did not occur during the polymerization.  相似文献   
53.
Photochemical vapor deposition of a-Si films at a high rate using SiH4 and a 185 nm low pressure mercury lamp is described. A maximum rate of 1 nm/sec was attained using the 185 nm lamp. This rate was about ten times higher than that using a 254 nm lamp. Assuming that there is no interaction between the effects of the two wavelengths, the deposition rate per light output power of 184.9 nm light is 160 times larger than that for 253.7 nm light. The absorption cross-section of the 184.9 nm light is ten times greater than that for the 253.7 nm light.  相似文献   
54.
Effects of the irradiation of ultrasound (US) on the photo-catalytic mineralization of some chlorinated organic compounds such as dichloroethane, tri- and tetrachloroethylenes, chloroacetic acids and chloromethanes were examined in oxygen saturated aqueous solutions suspended titanium dioxide (P25) particles. The yields of the sonochemical mineralization for these compounds were found to be extremely low compared to the photo-catalysis. However, the pre-sonication, US irradiation on the sample solution before the photo-irradiation, enhanced significantly the following photo-catalytic degradation to the complete oxidation. The effect was investigated in detail and it was found that the effect was mainly owing to the increase in the capability of the catalysis of which particles were sparsely dispersed by the sonication. The other contribution of the pre-sonication effect was found to be "pre-sonolysis", the initial formation of some intermediated products sonochemically, which are oxidizable more rapidly further to carbon dioxide than the original compound by the following photo-catalytic reactions. The pre-sonolysis effect was observed remarkably for trichloroacetic acid and tetrachloromethane, both of which are known to be hardly reactive to the photo-catalytic degradation. The photo-catalytic degradation with simultaneous sonication were also carried out for these compounds. The synergetic effect in the mineralization was observed both for carbontetrachloride and for trichloroacetic acid, the higher carbon dioxide yield being obtained in the simultaneous reaction than the sum of the yields in the photo-catalysis and the sonolysis each alone, while no significant synergetic effect was observed in the mineralization of other compounds.  相似文献   
55.
The dual Meissner effect is observed without monopoles in quenched SU(2) QCD with Landau gauge fixing. Magnetic displacement currents that are time-dependent Abelian magnetic fields act as solenoidal currents squeezing Abelian electric fields. Monopoles are not always necessary for the dual Meissner effect. A mean-field calculation suggests that the dual Meissner effect through the mass generation of the Abelian electric field is related to a gluon condensate A(a)(mu)A(a)(mu) not equal 0 of mass dimension 2.  相似文献   
56.
We present a 115In NMR study of the quasi-two-dimensional heavy-fermion superconductor CeCoIn5 believed to host a Fulde-Ferrel-Larkin-Ovchinnikov (FFLO) state. In the vicinity of the upper critical field and with a magnetic field applied parallel to the ab plane, the NMR spectrum exhibits a dramatic change below T*(H) which well coincides with the position of reported anomalies in specific heat and ultrasound velocity. We argue that our results provide the first microscopic evidence for the occurrence of a spatially modulated superconducting order parameter expected in a FFLO state. The NMR spectrum also implies an anomalous electronic structure of vortex cores.  相似文献   
57.
The hydrothermal synthesis, single crystal X-ray structures and magnetic properties of two layered cobalt-carboxylate complexes, 2[CoII(O2CCH(OH)C6H5)2] (1) and 2[CoII(O2CCH(NH2)C6H5)2] (2), where O2CCH(OH)C6H5 is mandalate and O2CCH(NH2)C6H5 is phenylglycinate, are described. Pale pink crystals of 1 and 2 were obtained by the reaction of cobalt nitrate and the enantiomer-pure acids at 120 °C. In each case, the structure consists of stacks of quasi square-grid polymeric sheets consisting of carboxylato- bridges, M-O-C-O-M, and the presence of both d- and l-enantiomers of the ligands segregated on each face of the layer. The ligands exhibit both chelating and bridging functions with the carboxylate group adopting an anti-anti mode. The magnetic properties are characteristic of weakly interacting paramagnets where the moments are elevated by an important orbital contribution via spin-orbit coupling.  相似文献   
58.
1,8-Bis(diphenylmethylium)naphthalenediyl dications promoted oxidative coupling of various N,N-dialkylanilines to afford the corresponding para-coupled bisanilines, benzidines, in good to excellent yield. The dications were readily prepared from a cyclic ether precursor, derived from 1,8-dibromonaphthalene, via deoxygenation with a silylating reagent in 1,1,1,3,3,3-hexafluoro-2-propanol under anhydrous conditions. [reaction: see text]  相似文献   
59.
Koshiba M  Saitoh K 《Optics letters》2004,29(15):1739-1741
We discuss the applicability of well-established classical optical fiber theories to holey fibers. By appropriately defining the V parameter, we can easily estimate the fundamental properties of holey fibers, such as effective index, group-velocity dispersion, mode field diameter, beam divergence, and splice loss, through simple empirical expressions without the need for heavy numerical computations. We confirm the validity of the V parameter defined here by comparing the calculated results with the earlier experimental and numerical results.  相似文献   
60.
Lipase TL-mediated kinetic resolution of (+/-)-5-benzyloxy-1-tert-butyldimethylsilyloxy-2-pentanol (5) at low temperature proceeded to give the corresponding (S)-alcohol 5 and (R)-acetate 6 in quantitative yields with high enantiomeric purity. The addition of bases such as pyridine, DMAP, 2,4- and 2,6-lutidines, or triethylamine considerably enhanced the rate of kinetic resolution. The alcohol (S)-5 and the acetate (R)-6 were converted to piperazic acid derivatives (R)- and (S)-3, respectively, via the intramolecular Mitsunobu reaction as a key step.  相似文献   
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