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排序方式: 共有969条查询结果,搜索用时 15 毫秒
1.
We introduce an impartial combinatorial game on Steiner triple systems called Next One to Fill Is the Loser (Nofil ). Players move alternately, choosing points of the triple system. If a player is forced to fill a block on their turn, they lose. By computing nim-values, we determine optimal strategies for Nofil on all Steiner triple systems up to order 15 and a sampling for orders 19, 21 and 25. The game Nofil can be thought of in terms of play on a corresponding hypergraph which will become a graph during play. At that point Nofil is equivalent to playing the game Node Kayles on the graph. We prove necessary conditions and sufficient conditions for a graph to reached playing Nofil. We conclude that the complexity of determining the outcome of the game Nofil on Steiner triple systems is PSPACE-complete for randomized reductions.  相似文献   
2.
考虑具有导子的李三系.由李三系和一个导子称为LietsDer对.定义系数在表示中的LietsDer对的上同调理论.研究LietsDer对的中心扩张.接下来,将形变理论推广到由李三系和导子构成LietsDer对上,它由带有系数的LietsDer对的上同调所支配.  相似文献   
3.
We investigate the coherent control of spin tunneling for a spin–orbit (SO) coupled boson trapped in a driven triple well. In the high-frequency limit, the quasienergies of the system are obtained analytically and the fine energy band structures are shown. By regulating the driving parameters, we reveal that the directed spin-flipping or spin-conserving tunneling of an SO-coupled boson occurs along different pathways and in different directions. The analytical results are demonstrated by numerical simulations and good agreements are found. Further, an interesting scheme of quantum spin tunneling switch with or without spin-flipping is presented. The results may have potential applications in the design of spintronic devices.  相似文献   
4.
A novel HIF (hypoxia-inducible factor)-1α inhibitor, the (aryloxyacetylamino)benzoic acid derivative LW6, is an anticancer agent that inhibits the accumulation of HIF-1α. The aim of this study was to characterize and determine the structures of the metabolites of LW6 in ICR mice. Metabolite identification was performed using a predictive multiple reaction monitoring-information dependent acquisition-enhanced product ion (pMRM-IDA-EPI) method in negative ion mode on a hybrid triple quadrupole-linear ion trap mass spectrometer (QTRAP). A total of 12 metabolites were characterized based on their MS/MS spectra, and the retention times were compared with those of the parent compound. The metabolites were divided into five structural classes based on biotransformation reactions: amide hydrolysis, ester hydrolysis, mono-oxidation, glucuronidation, and a combination of these reactions. From this study, 2-(4-((3r,5r,7r)-adamantan-1-yl)phenoxy)acetic acid (APA, M7), the metabolite produced via amide hydrolysis, was found to be a major circulating metabolite of LW6 in mice. The results of this study can be used to improve the pharmacokinetic profile by lowering the clearance and increasing the exposure relative to LW6.  相似文献   
5.
The triply bonded heavier main-group compounds have a textbook trans-bent geometry, in contrast to a familiar linear form found for the lightest analogues. Strikingly, the unexpected linear group 13 E≡E triple bonds were herein found in the D4h-symmetry E2Li62+ clusters, and they possess a large barrier (>18.0 kcal/mol) towards the dissociation of Li+. The perfectly surrounded Li4 motifs and two linear coordinated Li atoms strongly suppress the increasing nonbonded electron density of heavier E atoms, making two degenerate π bonds and one multi-center σ bond in linear heavier main-group triple bonds. The surrounding Li6 motifs not only creates an effective electronic structure to form a linear E≡E triple bond, but the resulting electrostatic interactions account for the highly stable global E2Li62+ clusters.  相似文献   
6.
Tricaine methanesulfonate is one of most commonly used anesthetics in fish during blood sampling, artificial propagation and long‐distance transportation. In this study, an accurate method for the quantitative determination of tricaine in fish samples by a stable isotope dilution assay coupled with high‐performance liquid chromatography–triple quadrupole mass spectrometry was developed. Tricaine‐D5 was synthesized and used as an isotopically labeled internal standard for the determination of tricaine. The analytical performance of the method was validated for tricaine determination in marine fish and freshwater fish. The determination of tricaine was linear in the range of 2.0–200.0 μg L?1. The limit of detection and limit of quantitation for fish muscle tissues were 1.0 and 4.0 μg kg?1, respectively. Good recoveries were obtained in the range of 92.08–97.50%. The inter‐ and intra‐assay relative standard deviations (RSD values) were investigated, and the values were 0.39–3.01 and 0.85–2.77%, respectively. The values of CCα and CCβ were 10.21–10.43 and 10.42–10.87 μg kg?1, respectively. The clearance of MS‐222 from grass carp was further studied using our method. The results demonstrate that MS‐222 could be well absorbed and rapidly eliminated after bath administration.  相似文献   
7.
In this study, a convenient and sensitive analytical method based on dispersive solid-phase extraction (dSPE) and gas chromatography-tandem mass spectrometry in tandem was developed for the simultaneous determination of six chloroacetamide herbicides (acetochlor, alachlor, metolachlor, metazachlor, butachlor and pretilachlor) in soil. Parameters that could influence the extraction efficiency such as the varieties of solvents, the amount of solvents and sorbents were investigated. The optimized extractions were performed by mixing 5.0 g of dried soil with 10.0 mL acetonitrile, 10.0 mL deionized water and 4.0 g sodium chloride, and then the extract was purified with 50.0 mg N-propyl ethylenediamine (PSA), 50.0 mg C18, 10.0 mg graphitized carbon black (GCB) and 100.0 mg MgSO4 (5:5:1:10). At 5.0, 25.0 and 100.0 ng g?1 fortification levels for each analyte, the average obtained recoveries ranged from 87.7% to 108.0% with relative standard deviation (RSD) between 3.8% and 10.9%. The soil matrix effect of the six compounds were lower than 11.0%. The linear relation was observed in the range of 5.0–500.0 ng g?1 and the correlation coefficient (R2) of these compounds were higher than 0.998. The detection limits (LODs) were in the range of 0.2–1.0 ng g?1, and the limits of quantification (LOQs) were between 0.8 and 2.2 ng g?1. Comparing with the gas chromatography-electron capture detector (GC-ECD), the GC-tandem mass spectrometry (MS/MS) method can improve the anti-interference ability and thus get better separation of the chloroacetamide herbicides. Additionally, this method was verified to fit for soil samples with broad organic matter range (16.2 to 83.0 g kg?1). The developed method was successfully applied for analysing 26 field soil samples collected from Dianchi lake basin in the southeast of China. About 42.0% soil samples were detected with these herbicides, of which butachlor was the most frequently detected and the highest concentration was up to 137.0 ng g?1 in rape soil.  相似文献   
8.
刘健  赵增勤  于文广 《数学学报》2019,62(3):441-448
在半直线无穷区间上,我们研究具有微小非自治扰动项的脉冲方程边值问题的古典解,应用变分方法和相应的临界点理论得到了三个古典解的存在性.  相似文献   
9.
The morphology evolution of carbide precipitated on grain boundary nearby different triple junctions in grain boundary engineering (GBE) treated nickel-based Inconel Alloy 690 aged at 715°C for different time was investigated by scanning electron microscopy and electron backscatter diffraction. The results show that, the diversity of triple junction types was increased by GBE significantly. The size and morphology of grain boundary carbide were not only affected by the grain boundary character, but also the nearby grain boundary character at the triple junction. The higher Σ values of the nearby grain boundaries, the larger carbide precipitated on the other grain boundary. Based on the experimental results, the effects of grain boundary characters and triple junction types on the carbide precipitation behaviours are discussed.  相似文献   
10.
Monodisperse silica spheres that comprised a rhombic‐dodecahedral zeolitic imidazolate framework core–shell microsphere were applied in the sample pretreatment of navel orange. A rapid and efficient liquid chromatography with triple quadrupole tandem mass spectrometry method was established for simultaneously quantifying four plant growth regulators, 6‐benzylaminopurin, indole‐3‐acetic acid, indolepropionic acid, 3‐indolebutyric acid, in navel oranges. A satisfactory result was obtained, i.e., the peak area of the four plant growth regulators against concentration was linear with good correlation coefficients of 0.99987–0.99991. Under optimized conditions, the limits of detection were 3.0–59.4 μg/L for the four plant growth regulators. This method was applied to the simultaneous analysis of the four plant growth regulators in commercial samples, and all the detections were confirmed by acquiring transitions for each pesticide in the samples.  相似文献   
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