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91.
A capillary electrophoresis (CE) method was developed for the separation of heparin oligosaccharides compatible to study the interactions between the oligosaccharides and granulocyte-colony stimulating factor (G-CSF). Unfractionated heparin was eliminitively degraded to heparin oligosaccharides by an endolytic heparinase. The degraded smaller oligosaccharides (M(r) < 1000) were baseline-separated by CE under a 50 mM phosphate buffer (pH 9.0) in 10 min. Standard heparin disaccharides and larger oligosaccharides (1000 < M(r) < 8000) were all separated under optimized separation conditions. Compared with standard heparin disaccharides, smaller oligosaccharides contained one nonsulfated, two monosulfated, and two disulfated disaccharides, but trisulfated disaccharides were not found. The smaller oligosaccharides were also identified and molecular mass was deduced by electrospray ionization-mass spectrometry (ESI-MS). Furthermore, interactions between G-CSF and the oligosaccharides were studied by using capillary zone electrophoresis (CZE) under the above separation conditions. It was found that larger oligosaccharides could interact with G-CSF while smaller oligosaccharides were not observed to bind to G-CSF under the experimental conditions. In conclusion, the purified heparinase could selectively degrade heparin into oligosaccharides and the interaction between G-CSF and heparin was correlated with the chain length of heparin. 相似文献
92.
A series of poly(ethylene glycol) biscoumarinyloxyacetatea have been synthesized and their intramolecular photochemical cyclodimerizations have been studied. It was found that only syn-HT configuration products were obtained when these bisesters were directly irradiated in chloroform, and the yields of the products decreased with the increase of the chain length. This photocyclization reaction is a convenient and effective method to synthesize macrocyclic compounds. 相似文献
93.
BEHAVIOR OF SUPPORTED NANO-COPPER CATALYST IN CO OXIDATION 总被引:1,自引:0,他引:1
IntroductionNanomaterialisanewkindofmaterialwithparticlesizebetWeenIurnand100urn.Becauseofthesmallparticlesizeandthelargespecificsufficearea,nanomaterialpossessesmanyparticularproperties,suchashighersufficeenergyandhighersurfaceactivity.t.[l]Thehigheracti… 相似文献
94.
物理有机化学是现代有机化学的主要理论基础,是当今有机化学中最富有活力的领域之一,它是建立在现代物理学和物理化学的基础上,用物理化学的、定量的、数学的方法来研究有机化学. 相似文献
95.
钙钛矿型复合氧化物对许多反应具有较高的催化活性,它们被广泛地用作CO氧化的催化剂.陈水华等对SmMeO_3(Me:V、Cr、Mn、Fe、Co)和Tascon等对LaMeO_3(Me:V、Cr、Mn、Fe、Co、Ni)上CO催化活性评价说明,LnMnO_3和LnCoO_3(Ln=La、Sm)活性最好,而LaNiO_3则表现和LaCoO_3相似活性,由此可推断这些氧化物具有相似的催化性能.本文用TPR-GC和XRD考察了在还原气氛下,LaNiO_3的还原机理,这对研究其电、磁特性具有一定的指导意义. 相似文献
96.
97.
Kwok WM Zhao C Guan X Li YL Du Y Phillips DL 《The Journal of chemical physics》2004,120(19):9017-9032
A combined experimental and theoretical study of the ultraviolet photolysis of CH2I2 in water is reported. Ultraviolet photolysis of low concentrations of CH2I2 in water was experimentally observed to lead to almost complete conversion into CH2(OH)2 and 2HI products. Picosecond time-resolved resonance Raman spectroscopy experiments in mixed water/acetonitrile solvents (25%-75% water) showed that appreciable amounts of isodiiodomethane (CH2I-I) were formed within several picoseconds and the decay of the CH2I-I species became substantially shorter with increasing water concentration, suggesting that CH2I-I may be reacting with water. Ab initio calculations demonstrate the CH2I-I species is able to react readily with water via a water-catalyzed O--H-insertion and HI-elimination reaction followed by its CH2I(OH) product undergoing a further water-catalyzed HI-elimination reaction to make a H2C=O product. These HI-elimination reactions produce the two HI leaving groups observed experimentally and the H2C=O product further reacts with water to produce the other final CH2(OH)2 product observed in the photochemistry experiments. These results suggest that CH2I-I is the species that reacts with water to produce the CH2(OH)2 and 2HI products seen in the photochemistry experiments. The present study demonstrates that ultraviolet photolysis of CH2I2 at low concentration leads to efficient dehalogenation and release of multiple strong acid (HI) leaving groups. Some possible ramifications for the decomposition of polyhalomethanes and halomethanols in aqueous environments as well as the photochemistry of polyhalomethanes in the natural environment are briefly discussed. 相似文献
98.
Ze-yong Zhao Wei-wei yao Rong-ni Du Qin Zhang Qiang Fu
Ze-hao Qiu Su-lan Yuan
《高分子科学》1996,(1):137-143
Ze-hao Qiu Su-lan Yuan
《高分子科学》1996,(1):137-143
A series of polydimethylsiloxane (PDMS) with varied molecular weights (Mw = 3 61620; 106, 1 61620; 106 and 0.5 61620; 106) were melt blended with PP to investigate the effect of PDMS molecular weight (MW) on the morphology and mechanical properties of PP/PDMS blends. Scanning electron microscopic (SEM) examination showed that the size of PDMS domains was dependent on the MW of PDMS. It was found that the lower the value of PDMS MW, the better dispersion of the PDMS domains in the PP matrix. Tensile and Izod impact tests revealed that the addition of PDMS with lower MW would lead to a more significant increase in impact strength of the blends compared with the blends with higher MW ones, while the influence of the molecular weight on tensile strengths of the blends was relatively small in the MW range studied. Differential scanning calorimetry (DSC) results also showed that the crystallization temperature of PP was increased with decreasing PDMS MW, indicating a better nucleation capability of lower MW of PDMS. Melting flow rate (MFR) measurements indicated that the processibility of PP could be enhanced by adding PDMS, and again the lower MW PDMS resulted in better data. Our work demonstrates that not only the processibility but also the mechanical properties of PP could be enhanced to a more significant degree by using low MW PDMS than the higher ones. 相似文献
99.
A novel sensitive method for the determination of nucleic acid (DNA) using the resonance light scattering (RLS) spectra of pentamethoxyl red has been developed. It is based on the effects on the resonance light scattering of Pentamethoxyl Red. The effective factors and the optimum conditions were studied, and the enhanced intensity of RLS is in proportion to the concentration of nucleic acids in the range of 0–2.54 µg mL−1 for ct-DNA, 0–4.54 µg mL−1 for hs-DNA. The limits of detection are 1.1 and 2.1 ng mL−1, respectively. Most foreign substances do not interfere in the determination, and the method has good selectivity and high sensitivity. It has been applied to the determination of DNA in synthetic samples and in real samples with satisfactory results. 相似文献
100.