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1.

Consider the following nonparametric model: \(Y_{ni}=g(x_{ni})+ \varepsilon _{ni},1\le i\le n,\) where \(x_{ni}\in {\mathbb {A}}\) are the nonrandom design points and \({\mathbb {A}}\) is a compact set of \({\mathbb {R}}^{m}\) for some \(m\ge 1\), \(g(\cdot )\) is a real valued function defined on \({\mathbb {A}}\), and \(\varepsilon _{n1},\ldots ,\varepsilon _{nn}\) are \(\rho ^{-}\)-mixing random errors with zero mean and finite variance. We obtain the Berry–Esseen bounds of the weighted estimator of \(g(\cdot )\). The rate can achieve nearly \(O(n^{-1/4})\) when the moment condition is appropriate. Moreover, we carry out some simulations to verify the validity of our results.

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2.
李林柯  汪淑敏  黄佳丽  雷寒  储涵  冯燕 《合成化学》2019,27(10):793-797
以咔唑为母体,设计并合成了一种可检测半胱氨酸的新型双光子荧光探针(3),其结构经1H NMR, 13C NMR, HR-MS(ESI)和元素分析表征。采用UV-Vis和FL研究了3的光学性能。结果表明:半胱氨酸加量为0~50 eq.时,3的紫外最大吸收峰从365 nm蓝移至342 nm;在350 nm处出现一个等吸收点;在450 nm处的荧光强度增强约23倍。  相似文献   
3.
As continuation of the work on fluorine, the second part of the studies of halogens in the air–acetylene flame attends to the determination of chlorine using high-resolution continuum source absorption spectrometry and molecular absorption. In case of chlorine, the diatomic InCl molecule proved to be a suitable species. For an excess of In in the flame, chlorine is converted to InCl which produces a distinctive band head at 267.24 nm that could be evaluated analytically. The influence of concentrated inorganic acids and metallic matrices on the absorption at this band head was tested. In all cases the signal proved to be unaffected, i.e., no spectral interferences were observed. However, serious chemical interferences were found in the presence of sulfuric and phosphoric acids, which could be partially eliminated by adding Ca in the form of nitrate. Moreover, nitric and hydrofluoric acids as well as Cu and Ga matrices also produced significant chemical interferences. Therefore, the method of standard additions should be used for calibration purposes. Concerning the limit of detection, a value of 3 mg L 1 was achieved for a measurement time of 5 s in the presence of 10,000 mg L 1 In. The calibration curve was linear up to a chlorine concentration of 1800 mg L 1. Three certified reference materials (BCR 151, HISS-1, and PACS-2) were analyzed to test the performance of the new method, yielding good precision and accuracy.  相似文献   
4.
《中国化学快报》2020,31(5):1213-1216
The widely accepted theory concerning the electrochemical energy storage mechanism of copper hexacyanoferrate (CuHCF) for supercapacitors is that CuHCF stores charge by the reversible redox processes of Fe3+/Fe2+ couple and Cu cations are electrochemically inactive. In this work, CuHCF nanocubes (CuHCF-NC) were synthesized in the presence of potassium citrate and its electrochemical properties were tentatively studied in 1 mol/L Na2SO4 aqueous electrolyte. Good supercapacitive performance was exhibited. The combined analyses of cyclic voltammogram (CV) and X-ray photoelectron spectroscopy (XPS) disclosed that the CuHCF nanocubes underwent the redox reactions of Fe3+/Fe2+ and Cu2+/Cu+ couples to store charges. The Cu2+/Cu+ redox couple was activated due to the strong coordination interaction between the carboxylate groups of citrate ions and surface Cu cations.  相似文献   
5.
High accuracy procedures for the determination of arsenic are needed for assigning reference values to certified reference materials (CRMs). There are a number of problems associated with the determination of total arsenic by inductively coupled plasma–mass spectrometry. Arsenobetaine (AsB) (the major species in fish) gives an enhanced response (9%) when compared to inorganic arsenic(V) and is very difficult to decompose. Chloride causes interference at m/z 75 by the formation of ArCl+ and chloride levels can be significant in marine fish. Also residual carbon in digests can lead to enhancement of arsenic signals by charge transfer effects. This can easily lead to erroneous quantification when compared to standards that do not contain carbon.This newly developed procedure overcomes these issues by complete mineralisation of the matrix leaving insignificant amounts of residual carbon and by removal of chlorine by evaporation. A detection limit of 30 ng/g was achieved. Recoveries for the following CRMs: DORM 2 100.1 ± 4.3%, SRM1548 96.1 ± 4.6%, BCR 422 103.6 ± 6.2% and SRM2976 105.9 ± 6.2% were obtained. The digestion procedure uses open vessel wet digestion with a mixture of sulfuric and nitric acid held at 300 °C. The decomposition of AsB was confirmed by speciation analysis of the digest. Carbon (m/z 13) was monitored to demonstrate the efficiency of the digestion. Instrumentation for the reduction of ArCl+ interference was not required and this view is supported by the recovery data. Measurements were performed by external calibration using tellurium as an internal standard.  相似文献   
6.
《Tetrahedron letters》2019,60(22):1493-1497
A simple and efficient method was developed for the synthesis of 1,4-thiazin-2-one O-(tert-butyl) oximes and benzo[b][1,4]thiazin-2-one O-(tert-butyl) oximes from N-tert-butoxy acyl imidoyl bromides and 2-aminothiols in the presence of K2CO3/SiO2. Twenty five novel compounds were readily synthesized in excellent yields using this procedure. The products possessed Z-stereochemistry with regard to the CN double bond. The reaction proceeded with initial substitution of bromine in the N-tert-butoxy acyl imidoyl bromides by mercapto groups in the presence of K2CO3/SiO2, and subsequent intramolecular Schiff base formation.  相似文献   
7.
A feasible proposal is explored to remotely perform a family of multi-qubit controlled-phase gates (MQCPG), with the aid of entanglement transfer and quantum repeater. To remotely realize the gates, some local transformations, including single-qubit rotating operation, controlled-NOT gate and quantum phase gate, are employed during the realization. It turns out that MQCPG can be implemented among separate spatially agents with nearly unit fidelity and success probability. Besides, required classical information consumption of the proposed scenario is worked out. Furthermore, some attractive issues are discussed including the feature of present proposal and the experimental feasibility based on current technologies. Remarkably, it is revealed that our proposal essentially accesses to several nontrivial features lying in breaking through the limitation that error probability scales exponentially with the length of the channel in the course of the realization of the gates, and well compatibility with today’s experimental technologies.  相似文献   
8.
9.
A series of Sm-CoMn substituted hexagonal ferrites with chemical composition of Sr0.85-xCa0.15SmxFe12-y(Co0.5Mn0.5)yO19 (0.00?≤?x?≤?0.60, (0.00?≤?y?≤?0.50) were synthesized by the solid-state reaction method. Microstructure and magnetic properties of the hexaferrites have been investigated by the X-ray diffraction, field emission scanning electron microscopy and a permanent magnetic measuring system. A single magnetoplumbite phase is exhibited in the hexaferrites with the substitutiom of Sm (0.00?≤?x?≤?0.12) and CoMn (0.00?≤?y?≤?0.10) contents. For the hexaferrites containing Sm (x?≥?0.24) and CoMn (y?≥?0.20), impurity phases are observed in the structure. The FESEM micrographs exhibit that the hexaferrites with different Sm-CoMn contents have formed hexagonal structures and the grain size of the hexaferrites remains unchanged with increasing Sm-CoMn content. The remanence (Br), Hk/Hcj ratios, and maximum energy product [(BH)max] decrease with increasing Sm-CoMn content (0.00?≤?x?≤?0.60, (0.00?≤?y?≤?0.50). Instrinsic coercivity (Hcj) and magnetic induction coercivity (Hcb) increase with increasing Sm-CoMn content (0.00?≤?x?≤?0.12, 0.00?≤?y?≤?0.10), and then decrease with increasing Sm-CoMn content (0.12?≤?x?≤?0.36, 0.10?≤?y?≤?0.30), while for the hexaferrites with Sm (x?≥?0.36) and CoMn (y?≥?0.30), with increasing Sm-CoMn content, Hcj increases and Hcb decreases.  相似文献   
10.
Sol–gel method is used to make a sequence of Barium based “X-type hexagonal ferrite (X-HF)” Ba2xDyxCu2Fe28 yCoyO46. “X-type hexagonal ferrites” with concentrations of “x = 0.0, 0.02, 0.06, 0.1 and y = 0.0, 0.1, 0.3, 0.5” are taken and the substitution impact of trivalent Dy3+ and divalent Co2+ is observed on the physical and magnetic properties of X-HFs. The XRD result, the refinement of which is accomplished using CelRef software validates the existence of pure single phase in these ferrites. Morphological structure of the crystal grains is calculated using electron microscopy and it is found that the grain has varying size in the range of 0.75–1.001 mm. FTIR analysis is done with and without the sintering process to examine the changes relevant to the structure and the chemistry of the material and the phases existed in the material. Thermogravimetric analyzer is used to measure the TGA and DSC quantities. All FTIR, DSC, and TGA results show that they are in good harmony with the results outcomes from XRD. “Vibrating sample magnetometer (VSM)” is used to quantify the magnetic properties of the sample under observation. It is observed that with an increase in the concentration of Dy-Co, Mr (Remanence) value decreases this could be reasoned by spin canting effect. The value of coercivity (Hc) changes from 317 to 158 G which follows the inverse relation between grain size and coercivity. The future use of the material may be in the microwave absorption devices.  相似文献   
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