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51.
Himabindu Nandivada Hsien‐Yeh Chen Joerg Lahann 《Macromolecular rapid communications》2005,26(22):1794-1799
Summary: The vapor‐based synthesis and characterization of a reactive polymer, poly[(4‐formyl‐p‐xylylene)‐co‐(p‐xylylene)] ( 1 ), have been reported. The reactive polymer coating enables the immobilization of oligosaccharides via the chemoselective aldehyde‐hydrazide coupling reaction.
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C3′‐Deoxygenation of Paromamine Catalyzed by a Radical S‐Adenosylmethionine Enzyme: Characterization of the Enzyme AprD4 and Its Reductase Partner AprD3 下载免费PDF全文
Hak Joong Kim Jake LeVieux Yu‐Cheng Yeh Prof. Dr. Hung‐wen Liu 《Angewandte Chemie (International ed. in English)》2016,55(11):3724-3728
C3′‐deoxygenation of aminoglycosides results in their decreased susceptibility to phosphorylation thereby increasing their efficacy as antibiotics. However, the biosynthetic mechanism of C3′‐deoxygenation is unknown. To address this issue, aprD4 and aprD3 genes from the apramycin gene cluster in Streptomyces tenebrarius were expressed in E. coli and the resulting gene products were characterized in vitro. AprD4 is shown to be a radical S‐adenosylmethionine (SAM) enzyme, catalyzing homolysis of SAM to 5′‐deoxyadenosine (5′‐dAdo) in the presence of paromamine. [4′‐2H]‐Paromamine was prepared and used to show that its C4′‐H is transferred to 5′‐dAdo by AprD4, during which the substrate is dehydrated to a product consistent with 4′‐oxolividamine. In contrast, paromamine is reduced to a deoxy product when incubated with AprD4/AprD3/NADPH. These results show that AprD4 is the first radical SAM diol‐dehydratase and, along with AprD3, is responsible for 3′‐deoxygenation in aminoglycoside biosynthesis. 相似文献
53.
Effects of substituent and solvent on the structure and spectral properties of maleimide derivatives
Chin-Kuen Tai Yih-Jiun Lin Pao-Ling Yeh Yi-Ren Tzeng Yu-Ma Chou Bo-Cheng Wang 《Journal of Molecular Structure》2008,860(1-3):58-63
The maximum absorption wavelength , emission wavelength (λem) and the related oscillator strength (f) of the maleimides in the ground and first excited states were calculated by using the DFT, CIS and the time-dependent density functional theory (TD-DFT) methods, where the molecular structures were optimized by DFT/B3LYP/6-31G* calculation. Solvent effects on the maleimides were examined using the PCM simulation at DFT/B3LYP level with the 6-31G* basis set. For N-substituted maleimide, the substituent gives only a slight influence on the maleimide chromophore, while planar conformation of PhMLH leads to the improvement in π-delocalization from substituent to maleimide unit. For 3,4-substituted maleimide, the steric repulsion between substituent and maleimide chromophore influences the extent of π-delocalization and the molecular conformation. The calculated and λem of maleimides are in good agreement with the experimental data. In the gas phase, both absorption and emission peaks are red-shift as compared to the non-substituted maleimide. Under solvent environment, the more planar conformation of PhMLH shows a blue-shift in the calculated and λem as compared with other N-substituted maleimides. For 3,4-substituted maleimides, the effect of substitution produces the most significant spectral red-shift as compared to other maleimides. 相似文献
54.
A differential radial distribution function (DRDF) of molten natural rubber (NR) was derived from its wide-angle x-ray scattering (WAXS) data. Three peaks with Bragg spacings 4.85, 2.31, and 1.23 Å corresponding, respectively, to interchain, C1-C3 and C1 -C2 distances are present in the corrected WAXS curve. The derived DRDF, which is shown to be greatly improved than the ones published so far, contains six peaks located at 1.51, 2.48, 3.98, 5.68, 10.65, and 15.25 Å. Maximum contributions of intramolecular atomic distances to the radial distribution peaks were estimated and compared with the experimental results. The comparison shows that the first three peaks are intramolecular in origin and the remaining peaks are predominantly due to intermolecular regularities. A periodicity of an approximately constant interval of 5.26 Å is found between the intermolecular peaks and is attributable to the organizations of more or less parallel chain segments in the material. This finding provided additional evidence for the presence of local lateral ordering to the extent of about 30 Å in molten-state natural rubber. 相似文献
55.
Dot-matrix holograms created by two-beam writers contain many grating dots. Because the phase difference between two laser beams for interference cannot be controlled accurately, the fringe positions of grating dots are randomly determined. Therefore, fringe positions are a good kind of tool to identify dot-matrix holograms. In this paper, a number difference between two special fringes of a target grating dot is used to identify a dot-matrix hologram. The two special fringes are determined by three grating dots with parallel fringes. The first special fringe is corresponding to a fringe pair with the best matching for the fringes of the target grating dot and the fringes of the second grating dot. The second special fringe is corresponding to a fringe pair with the best matching for the fringes of the target grating dot and the fringes of the third grating dot. An experiment has proved the proposed method practical and feasible. Because reproducing a grating dot with a specified fringe number difference is difficult, the proposed method is excellent for anti-counterfeiting. 相似文献
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Chen C. Y. Kao C. L. Yeh H. C. Li H. T. Wu M. D. Cheng M. J. Li W. J. 《Chemistry of Natural Compounds》2022,58(3):385-386
Chemistry of Natural Compounds - A new ketone, vicamazone (4-(2-butoxyethoxy)-4-methylpentan-2-one) (1), was isolated from the leaves of Victoria amazonica (Nymphaeaceae). The structure of the new... 相似文献
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