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991.
Pan Xue Yongming Li Zhujun Zhang Aihua Fu Fei Liu Xiaoming Zhang Yuanjie Sun Lili Chen Boquan Jin Kun Yang 《Mikrochimica acta》2011,174(1-2):167-174
An enzyme-linked immunosorbent assay, a horseradish peroxidase-catalyzed fluorogenic reaction, and chemiluminescence (CL) analysis have been combined to develop a sandwich ELISA for Staphylococcal enterotoxin B (SEB) using monoclonal antibodies for different epitopes of SEB. The enzyme catalyzed reaction of 3-(4-hydroxyphenyl propionate) with the urea complex of hydrogen peroxide produced a fluorescent dimer which was detected by chemiluminescence analysis. The CL response to SEB is linear in the range from 6.0 to 564?pg?mL?1 (r?=?0.9993), and the detection limit is 3.3?pg?mL?1 (S/N?=?3). Intra- and interassay coefficients of variation are <7.0% at three concentrations (24, 96 and 384?pg?mL?1). The method was applied to the analysis of SEB in serum, lake water and milk samples. The results compared well with those obtained by conventional ELISAs. Figure
Procedures of the proposed method. A sandwich ELISA for Staphylococcal enterotoxin B (SEB) using a pair of monoclonal antibodies that recognizes different epitopes of SEB. After the ELISA procedure, PHPPA is reacted with Hydrogen peroxide-urea, with catalysis by HRP-conjugated anti-SEB, to produce PHPPA fluorescent Dimer, which is detected by TCPO chemiluminescence. 相似文献
992.
Guanglei LvGenping Huang Guangyou ZhangChangduo Pan Fan Chen Jiang Cheng 《Tetrahedron》2011,67(26):4879-4886
A rhodium or palladium-catalyzed addition of boronic acids to phthalaldehydonitrile, followed by an intramolecular lactonization of cyano to access 3-substituted phthalides, is described. This procedure tolerates a series of functional groups, such as methoxy, fluoro, chloro, and vinyl groups. It is a novel procedure for the synthesis of 3-arylphthalides. 相似文献
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997.
A hevein-like protein and a class I chitinase with antifungal activity from leaves of the paper mulberry 总被引:1,自引:0,他引:1
Paper mulberry (Broussonetia papyrifera, syn. Morus papyrifera L.) is a Chinese traditional medicine and its low‐molecular‐weight extracts are reported to have antifungal activity. In this study, two proteins (PMAPI and PMAPII) with activity against Trichoderma viride were obtained from paper mulberry leaves with a fast protein liquid chromatography (FPLC) unit. The purification protocol employed (NH4)2SO4 precipitation, ion‐exchange chromatography and hydrophobic‐interaction chromatography on FPLC. Molecular masses were 18,798 Da for PMAPI, and 31,178 Da for PMAPII determined by Matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry. Peptide mapping fingerprint analysis showed that PMAPI has no peptides similar to PMAPII. N‐terminal amino acid sequencing revealed that PMAPI is a hevein‐like protein, and PMAPII is a class I chitinase. They both had a half‐maximal inhibitory concentration (IC50) of 0.1 µg/µL against T. viride. This is the first report of high‐molecular‐weight extracts with antifungal activity from paper mulberry. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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999.
Spatial bandgap engineering along single alloy nanowires 总被引:1,自引:0,他引:1
Gu F Yang Z Yu H Xu J Wang P Tong L Pan A 《Journal of the American Chemical Society》2011,133(7):2037-2039
Bandgap engineering of semiconductor nanowires is important in designing nanoscale multifunctional optoelectronic devices. Here, we report a facile thermal evaporation method, and realize the spatial bandgap engineering in single CdS(1-x)Se(x) alloy nanowires. Along the length of these achieved nanowires, the composition can be continuously tuned from x = 0 (CdS) at one end to x = 1 (CdSe) at the other end, resulting in the corresponding bandgap (light emission wavelength) being modulated gradually from 2.44 eV (507 nm, green light) to 1.74 eV (710 nm, red light). In spite of the existing composition (crystal lattice) transition along the length, these multicolor nanowires still possess high-quality crystallization. These bandgap engineered nanowires will have promising applications in such as multicolor display and lighting, high-efficiency solar cells, ultrabroadly spectral detectors, and biotechnology. 相似文献
1000.
We demonstrate that the vacuum ultraviolet (VUV) photodissociation dynamics of N(2) and CO(2) can be studied using VUV photoionization with time-sliced velocity-mapped ion imaging (VUV-PI-VMI) detection. The VUV laser light is produced by resonant sum frequency mixing in Kr. N(2) is used to show that when the photon energy of the VUV laser is above the ionization energy of an allowed transition of one of the product atoms it can be detected and characterized as the wavelength is varied. In this case a β parameter = 0.57 for the N((2)D°) was measured after exciting N(2)(o(1)Π(u), v(') = 2, J(') = 2) ← N(2)(X(1)Σ(g) (+), v(") = 0, J(") = 1). Studies with CO(2) show that when there is no allowed transition, an autoionization resonance can be used for the detection of a product atom. In this case it is shown for the first time that the O((1)D) atom is produced with CO((1)Σ(+)) at 92.21 nm. These results indicate that the VUV laser photodissociation combined with the VUV-PI-VMI detection is a viable method for studying the one-photon photodissociation from the ground state of simple molecules in the extreme ultraviolet and VUV spectral regions. 相似文献