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291.
We study a matrix model obtained by dimensionally reducing Chern–Simons theory on S3S3. We find that the matrix integration is decomposed into sectors classified by the representation of SU(2)SU(2). We show that the N  -block sectors reproduce SU(N)SU(N) Yang–Mills theory on S2S2 as the matrix size goes to infinity.  相似文献   
292.
Although molecular bromine (Br2) is a useful brominating reagent, it is not easy to handle. Herein, we describe the preparation of a novel air-stable bromine complex prepared from 1,3-dimethyl-2-imidazolidinone (DMI) and Br2, which was identified to be (DMI)2HBr3 by spectral and X-ray techniques. This complex was then used to brominate olefins, carbonyl compounds, and aromatics, as well as in the Hofmann rearrangement. Yields of reaction products using this complex were almost the same or superior to those using other bromine alternatives.  相似文献   
293.
A 5-endo-trig alkene insertion proceeds under palladium catalysis via aminopalladium species starting from 3,3-difluoroallyl ketone O-pentafluorobenzoyloximes, providing a facile access to 5-fluoro-3H-pyrroles.  相似文献   
294.
295.
Let T be a bounded linear operator on a complex Hilbert space H. T $/in$ B(H) is called a log-hyponormal operator if T is invertible and log (TT *) log (T * T). Since a function log : (0,) (-,) is operator monotone, every invertible p-hyponormal operator T, i.e., (TT *) p (T * T p is log-hyponormal for 0 < p 1. Putnams inequality for p-hyponormal operator T is the following:$ \| (T^*T)^p-(TT^*)^p \|\leq\frac{p}{\pi}\int\int_{\sigma(T)}r^{2p-1}drd\theta $.In this paper, we prove that if T is log-hyponormal, then$ \| log(T^*T)-log(TT^*) \|\leq\frac{1}{\pi}\int\int_{\sigma(T)}r^{-1}drd\theta $.  相似文献   
296.
2,4-Dienoate was prepared by pyrolysis of 2-(phenylsulfinyl)enoate. N-Isobutyl-E,E-2,4-decadieneamide (pellitorine) was synthesized from decanoic acid in a satisfactory yield.  相似文献   
297.
The potential dependence of surface-enhanced resonance Roman spectra of meso-tetrakis (4-sulfonatophenyl) porphine (TSPP) in 0.05 M H2SO4 reveals two electrochemical processes at a silver electrode surface. One which begins around ?0.3 V is interpreted as dissociation of aggregated TSPP to monomers. The other which occurs near ?0.4 V is ascribed to a partial Ag incorporation of TSPP molecules.  相似文献   
298.
The time resolved product formation in oxidation of dimethyl ether (DME) has been studied between 298-625 K and 20-90 torr total pressure. Near-infrared frequency modulation spectroscopy (FMS) with Herriott type multi pass optics and UV absorption spectroscopy (UV) were conducted in the same cell. The reaction was initiated by pulsed photolysis in a mixture of Cl2, O2, and DME via CH3OCH2 radical formation. The reaction process was investigated through FMS measurement of HO2 and OH, and UV measurement of CH3OCH2O2. The yields of HO2 and OH are obtained by comparison with reference mixtures, Cl2, O2, and CH3OH for HO2, and Cl2, O2, CH3OH, and NO for OH, which convert 100% of initial Cl to HO2 and OH. The CH3OCH2O2 yield is also obtained. It was found that the HO2 yield increases sharply over 500 K mainly with a longer time constant than that of R + O2 reaction, while a prompt component exists throughout the temperature range at a few percent yield. OH was found to be produced promptly at a yield considerably larger than that known for the simplest alkanes. The CH3OCH2O2 profile has a prompt rise followed by a gradual decay whose rate is consistent with the slow HO2 formation. The species profiles were successfully predicted with a model constructed by modifying the existing one to suit the reduced pressure condition. After modification, it was inferred that the HO2 formation over 500 K is secondary from HCHO + OH and HCO + O2 and a part of HCO is formed directly from the O2 adduct, whereas the HO2 formation below 500 K is governed by CH3OCH2O2 chemistry. The HCO forming pathway via isomerization-decomposition of the O2 adduct, which was not included in the former models, was supported by our quantum-chemical calculations.  相似文献   
299.
High-resolution electron spin resonance (ESR) spectra of radical pairs of a hydrogen atom that coupled with a methyl radical (H...CH3, H...CHD2, D...CH2D, and D...CD3) were observed for X-ray irradiated solid argon containing selectively deuterium-labeled methanes, CH4, CH2D2, and CD4, at 4.2 K. The double-quartet 1H-hyperfine (hf) splittings of ca. 26 and 1.16 mT at the Deltam(s) = +/-1 and Deltam(s) = +/-2 transitions, which are one-half of the isotropic 1H-hf splittings of an isolated H-atom and a CH3 radical, were attributed to the H...CH3 pair. The 1H-hf splittings at the Deltam(s) = +/-1 transition were further split by the fine structure (fs) due to the electron dipole-dipole coupling. Because of the high-resolution spectra, three different sets of the fs splitting, d, are clearly resolved in the spectra of both the H...CH3 and the D...CD3 pairs. The separation distance (inter-spin distance), R, between the H-atom and the CH3 radical being in pairs was evaluated from the d values based on a point-dipole interaction model. For the case of the H...CH3 pair, the observed d values of 4.2, 4.9, and 5.1 mT yield the respective separations, R = 0.87, 0.83, and 0.82 nm, to probe the trapping site of the pair in an Ar crystalline lattice (fcc). For the pair with R = 0.87 nm, for example, we propose that the CH3 radical occupies a substitutional site and the counter H-atom occupies either the interstitial tetrahedral sites directed away from the CH3 radicals by a distance of 0.87 nm or the interstitial octahedral sites by a distance of 0.88 nm. When a mixture of CH4 and CD4 in a solid Ar matrix was irradiated, only two different radical pairs, H...CH3 and D...CD3, were observed. This result clearly demonstrates that the hydrogen atom and methyl radicals, which undergo a pairwise trapping, can originate from the same methane molecule.  相似文献   
300.
A new class of polymerizations was developed via metal-catalyzed C-C bond forming radical polyaddition; the monomers were designed to have a reactive C-Cl bond, which can be activated by the metal catalysts to generate a carbon radical species, along with a C=C double bond, to which the carbon radical generated from another molecule adds to form a C-C backbone polymer with an inactive C-Cl pendant.  相似文献   
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