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21.
采用高效液相色谱法,以9-蒽醛为衍生试剂,在5种多糖衍生物的手性固定相(CSPs)上对几种α-氨基酸甲酯对映体进行了手性分离。色谱条件如下: 流动相为含3%~10%(v/v)异丙醇的正己烷溶液,流速为1.0 mL/min,检测波长为254 nm。结果表明,α-氨基酸甲酯-9-蒽醛亚胺衍生物在Chiralcel OD柱或Chiralcel OD-H柱上的手性分离结果优于其他CSPs,而且在Chiralcel OD柱或Chiralcel OD-H柱上全部得到了基线拆分(α=1.24~5.47, Rs=2.56~13.90), L-对映体在这两种色谱柱上的保留强于D-对映体。同时还考察了几种脂肪胺在5种多糖衍生物手性固定相上的对映体拆分效果,结果表明脂肪胺的9-蒽醛亚胺衍生物在Chiralcel OD柱或Chiralcel OD-H柱上的分离效果良好。该法可用于其他α-氨基酸酯和胺类化合物对映体的分析。 相似文献
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A rigorous finite element analysis procedure is developed to study the effect of the inner structures on the acoustic absorption of multi-layer absorbers. To do this, four types of basic inner structure compartments adopted in the multi-layer absorbers are selected for analysis. These compartments are composed of porous materials inlaid with perforated plates of various shapes, say, triangle, semicircle, convex rectangle and plate shapes. As it is different from the conventional finite element analysis for the acoustic system in the literature, the perforated plates are simulated by appropriate equivalent boundary conditions, depending on their thickness, hole radius, hole pitch and porosity and the air contained in the holes. A large number of total degrees of freedom generated from meshing the air in the holes of perforated plates are thus avoided. The results reveal that the inner structures of the multi-layer absorbers will influence the acoustic absorption at some frequency bands significantly. Based on those features, the multi-layer absorber with a novel inner structure is then designed and manufactured. Both the finite element and experimental results show that its acoustic absorption would be distinctly promoted. 相似文献
24.
广州市住宅室内外大气羰基化合物的监测分析 总被引:5,自引:0,他引:5
选择代表性住宅,在其室内、外同步开展大气羰基化合物的监测分析,准确评价大气羰基化合物的污染状况,揭示其来源。用涂覆2,4-硝基苯肼(DNPH)的硅胶采样管收集羰基化合物,借助高效液相色谱完成样品分析,共检测了13种羰基化合物,其中甲醛、乙醛两种物质的平均浓度最高,占被测物质总浓度的30%~67%。甲醛、乙醛的浓度,夏季室内平均为53.47μg/m3、17.81μg/m3,室外平均为15.00μg/m3、10.97μg/m3;冬季室内平均为37.97μg/m3、11.49μg/m3,室外平均为10.44μg/m3、8.15μg/m3。大气羰基化合物呈现夏季高于冬季、室内大于室外的浓度变化规律。甲醛/乙醛和乙醛/丙醛比值结果反映城市大气羰基化合物的人为污染。 相似文献
25.
A dammarane derivative dihydrojujubogenin-2-en-1-one, which possesses a skeleton and pharmacophore partially similar to those of Territrem B, a potent AChE inhibitor, was synthesized via three different paths. The anti-AChE activity of this compound and related analogue was measured. 相似文献
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A viscosity method for a hierarchical fixed point solving variational inequality problems is presented. The method is used to solve variational inequalities, where the involved mappings are non-expansive. Solutions are sought in the set of the fixed points of another non-expansive mapping. As applications, we use the results to study problems of the monotone variational inequality, the convex programming, the hierarchical minimization, and the quadratic minimization over fixed point sets. 相似文献
28.
The structures, energies, Spectra, and charge transfer to solvent (CTTS) energies of the hydrated superoxide anion clusters have been investigated using both density functional calculations (DFT) with Becke-3-parameters employing Lee-Yang-Parr functionals (B3LYP) and second-order M?ller Plesset perturbation (MP2) calculations employing highly diffuse basis sets. Given the good agreement of our predicted results with the experimental spectra and enthalpy, it would be interesting if the CTTS energies could be experimentally determined. 相似文献
29.
气化是实现化学利用碳资源(尤其是煤)生产化学品和燃料的关键工艺.目前,全球拥有超过272套气化装置,主要应用于煤化工,尤其在中国.由于在一个化工厂通过技术集成达到工业规模的集中生产可实现减少二氧化碳排放并促进碳密集型行业的循环经济,如废物管理、化学和交通行业,因此,近年来全球对垃圾气化的兴趣日益浓厚,尤其是那些在煤气化... 相似文献
30.
LEE H. PrattYukio SMMAZAKIT†Yasunori Inoue†Masaki Furuya† 《Photochemistry and photobiology》1982,36(4):471-477
Phototransformation of the red-absorbing form of phytochrome (Pr) to the far-red-absorbing form (Pfr) was followed with a custom-built transient spectrum analyzer. Large phytochrome, which consisted of approximately 120000-dalton monomers, was immunopurified or conventionally purified from etiolated oat (Avena sativa L., cv. Garry) shoots. Phototransformation was initiated by exciting Pr with a 115-mJ, 600-ns half-width, 655-nm laser pulse. Absorption spectra were recorded on a microsecond time scale at predetermined times after the flash. It has been reported earlier that flash excitation of large oat Pr produces a transformation intermediate with maximum absorbance near 700 nm in a difference spectrum and that this intermediate decays by two kinetically distinct reactions. Difference spectra for these two reactions are indistinguishable. Both show bleaching centered at 690 nm with no detectable associated absorbance increase between 570 and 830 nm. Subsequent appearance of absorbance at 724 nm, which presumably but not necessarily represents the appearance of Pfr, had earlier been shown to occur by two kinetically distinct reactions for large oat phytochrome. Data presented here indicate in addition the occurrence of a third, slower reaction. Difference spectra for the two faster reactions are indistinguishable, both with maxima near 728 nm and minima near 650 nm. The difference spectrum for the slowest component, however, was qualitatively different exhibiting a maximum near 722 nm with no corresponding minimum. About 15-20% of the absorbance increase at 724 nm occurred by this slowest reaction, which exhibited a half-life of 3 s at 25°C and a Q10 of 1.2 for immunopurified and 1.5 for conventionally purified phytochrome. The percentage occurring by this reaction was independent of temperature over the range studied (1-25dEC). For immunopurified phytochrome the enthalpy of activation, Gibbs free energy of activation, and entropy of activation of this slowest reaction were found to be about lOkJ-mol-1, 75kJ.mol-1, and -220 J.mol-1 K-1, respectively, and for conventionally purified phytochrome 25kJ.mol-1, 75kJ.mol-1and —170 J.mol-1 K-1, respectively. The thermodynamic characteristics of this reaction indicate that it may involve a significant ordering of the protein moiety as it transforms to Pfr. 相似文献