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171.
A series of aluminum dimethyl complexes 1 – 6 bearing N‐[2‐(pyrrolidinyl)benzyl]anilido ligands were synthesized and well characterized. The molecular structure of complex 1 determined by an X‐ray diffraction study indicates the bidentate chelating mode of the pyrrolidinyl‐anilido ligand. In the absence of a coinitiator, these complexes exhibited excellent control toward the polymerizations of ε‐caprolactone and rac‐lactide, affording polyesters with quite narrow molecular weight distributions (Mw/Mn = 1.04–1.26). The end group analysis of ε?CL oligomer via 1H NMR and ESI‐TOF MS methods gave strong support to the hypothesis that the polymerization catalyzed by these aluminum complexes proceeds via a coordination‐insertion mechanism involving a unique Al? N (amido) bond initiation. Via 1H NMR scale oligomerization studies, it is suggested that the insertion of the first lactide monomer into Al? N bond of the complex is much easier than the insertion of lactide monomer into the newly formed Al? O (lactate) bond and might also be easier than the insertion of the first ε?CL monomer into Al? N bond. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3096–3106 相似文献
172.
Mechanistic investigation of imine formation in ruthenium‐catalyzed N‐alkylation of amines with alcohols 下载免费PDF全文
Imines are observed frequently in ruthenium‐catalyzed N‐alkylation of amines with alcohols. Herein, nitrogen–phosphine functionalized carbene ligands were developed and used in ruthenium‐catalyzed N‐alkylation to explore the mechanism of imine formation. The results showed that strongly electron‐donating ligands were beneficial for imine formation and alcohol dehydrogenation to generate acid. In addition, with an increase of electron density of nitrogen atom in substituted amines, the yield of imines in N‐alkylation was improved. At the same time, with electron‐rich imines as substrates, the transfer hydrogenation of imines became difficult. It is suggested that strongly electron‐donating ligands and substrates caused an increase of electron density on the ruthenium center, which resulted in the elimination of hydrogen atoms in active species [LRuH2] as hydrogen gas rather than transfer onto the imine coordinated with the ruthenium center. 相似文献
173.
In this paper, the nonlinear dynamical behavior of two coupled pipes conveying pulsating fluid is studied. The connection between the two pipes is considered as a distributed linear spring. Based on this consideration, the equations of motion of the coupled two-pipe system are obtained. The two coupled nonlinear partial differential equations, discretized using the fourth- order Galerkin method, are solved by a fourth-order Runge-Kutta integration algorithm. Results show that the connection stiffness has a significant effect on the dynamical behavior of the coupled system. It is found that for some parameter values the motion types of the two pipes might be synchronous. 相似文献
174.
175.
Song Zhongxian Fu Yongmei Ning Ping Liu Hongpan Ren Dong Kang Haiyan Liu Biao Mao Yanli Guo Yifei Zhang Qiulin 《Research on Chemical Intermediates》2019,45(4):2313-2326
Research on Chemical Intermediates - The effect of different pH values (8, 9, 10 and 11) on the catalytic activity over CeSiW catalysts was investigated for the selective catalytic reduction of NO... 相似文献
176.
Xiaomin Xu Xiaohong Ding Bo Yuan Weiwei Li Yimei Wang Yi Jin Haiyan Xu 《Biomedical chromatography : BMC》2019,33(6)
A rapid, simple and sensitive LC–MS/MS method was established and validated for simultaneous quantification of ticagrelor and its active metabolite AR‐C124910XX in human plasma. After plasma samples were deproteinized with acetonitrile, the post‐treatment samples were chromatographed on a Dikma C18 column interfaced with a triple quadrupole tandem mass spectrometer. Electrospray negative ionization mode and multiple reaction monitoring were adopted to assay ticagrelor and AR‐C124910XX. Acetonitrile and 5 mΜ ammonium acetate was used as the mobile phase with a gradient elution at a flow rate of 0.5 mL/min. The method was linear in the range of 0.781–800 ng/mL for both ticagrelor and AR‐C124910XX with a correlation coefficient ≥0.994. The intra‐ and inter‐day precisions were within 12.61% in terms of relative standard deviation and the accuracy was within ±7.88% in terms of relative error. The LC–MS/MS method was fully validated for its sensitivity, selectivity, stability, matrix effect and recovery. This convenient and specific LC–MS/MS method was successfully applied to the pharmacokinetic study of ticagrelor and AR‐C124910XX in healthy volunteers after an oral dose of 90 mg ticagrelor. 相似文献
177.
Yi Song Jiang-Li Ni Zhang-Yin Wang Yan Lu Lian-Fang Han 《International Journal of Theoretical Physics》2017,56(10):3175-3187
We present a new scheme for deterministically realizing the mutual interchange of quantum information between two distant parties via selected quantum states as the shared entangled resource. We first show the symmetric bidirectional remote state preparation (BRSP), where two single-qubit quantum states will be simultaneously exchanged in a deterministic manner provided that each of the users performs single-qubit von Neumann measurements with proper measurement bases as well as appropriate unitary operations, depending essentially on the outcomes of the prior measurements. Then we consider to extend the symmetric protocol to an asymmetric case, in which BRSP of a general single-qubit state and an arbitrary two-qubit state is investigated successfully. The necessary quantum operations and the employed quantum resources are feasible according to the present technology, resulting in that this protocol may be realizable in the realm of current physical experiment. 相似文献
178.
Hydride generation atomic fluorescence spectrometry (HG-AFS) is used for the determination of hydride-forming elements due to its high sensitivity, simplicity, and low cost. A new HG-AFS method for the simultaneous determination of arsenic and lead in vegetable oil is reported. Vortex-assisted extraction with dilute nitric acid was used to isolate arsenic and lead from vegetable oil. The conditions influencing the fluorescence signal, including the carrier fluid, oxidizing agent, and reducing agent, were optimized. The interferences of coexisting ions were also evaluated. Under the optimized conditions, the limits of detection were 0.6 and 0.4?µg?kg?1 for arsenic and lead. The recoveries were from 84.4 to 105% for both metals in vegetable oil. The optimized method was used for the determination of arsenic and lead in commercial vegetable oil. The analytical results by this approach were in good agreement with values obtained by inductively coupled plasma mass spectrometry with microwave digestion. 相似文献
179.
Applied Mathematics and Mechanics - The recently developed hard-magnetic soft (HMS) materials can play a significant role in the actuation and control of medical devices, soft robots, flexible... 相似文献
180.
Liu Yuanyuan Zhou Weibo Liu Haiyan Wei Qianglin Gao Bai Chen Gongxin 《Journal of Radioanalytical and Nuclear Chemistry》2020,324(1):33-42
Journal of Radioanalytical and Nuclear Chemistry - The concentrations of 238U, 226Ra, 232Th and 40K and gross α, β were measured in soils and sediments around a uranium tailings reservoir... 相似文献