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841.
842.
A stability-indicating HPLC assay has been developed for 2-{4-[(7-chloro-2-quinoxalinyl)oxy]phenoxy}propanoic acid (XK469). XK-469 is the 7-chloro analog of herbicide Quizalofop and is currently under development as an antineoplastic agent. HPLC separation of XK469 is achieved with an ODS column using isocratic elution of an aqueous MeOH mobile phase. The assay is reproducible (RSD=0.9%), linear (r2=0.999), accurate (error=1.2%) and sensitive (LDL=1.2 ng). The HPLC separates XK469 from its forced decomposition products. Identities of the decomposition products have been elucidated. 相似文献
843.
Aldimines derived from aryl and non-enolizable aliphatic aldehydes were allylated with allyl bromide mediated by indium powder in [bpy][BF4] (bpy = N-butylpyridine) to give good yields of the corresponding homoallylic amines. Selective formation of monoallylated amines can be achieved by varying the amount of bromide ion additive in the form of [bpy][Br]. The transient organoindium intermediates, allylindium(I) and allylindium(III) dibromide formed in the reaction, were studied by NMR spectroscopy to explain the selectivity. 相似文献
844.
This article reviews the applications of CE that are relevant to the analysis of small molecules in foods. CE has been applied to a wide range of important areas of food analysis and is rapidly being established as an alternative technique to chromatographic methods including HPLC and GC within analytical food and research laboratories. In recent years the analysis of food by CE has become more frequent and important and as such a variety of compounds have been separated and quantified. Although many other analytes have been detected by CE, this review will highlight areas relating primarily to the rather broad chemical classes of free amino acids, carbohydrates, organic acids, vitamins and a variety of antioxidants. In addition, information relating to the analyte, sample matrix, mode of CE employed, scope of the methodology and the detection and derivatization of the small molecules are considered and discussed. 相似文献
845.
Multistage dynamic networks with random arc capacities (MDNRAC) have been successfully used for modeling various resource allocation problems in the transportation area. However, solving these problems is generally computationally intensive, and there is still a need to develop more efficient solution approaches. In this paper, we propose a new heuristic approach that solves the MDNRAC problem by decomposing the network at each stage into a series of subproblems with tree structures. Each subproblem can be solved efficiently. The main advantage is that this approach provides an efficient computational device to handle the large-scale problem instances with fairly good solution quality. We show that the objective value obtained from this decomposition approach is an upper bound for that of the MDNRAC problem. Numerical results demonstrate that our proposed approach works very well. 相似文献
846.
The latest CDF anomaly, the excess of dijet events in the invariant-mass window 120-160 GeV in associated production with a W boson, can be explained by a baryonic Z' model in which the Z' boson has negligible couplings to leptons. Although this Z' model is hardly subject to the Drell-Yan constraint from Tevatron, it is constrained by the dijet data from UA2 (√s=630 GeV), and the precision measurements at LEP through the mixing with the SM Z boson. We show that under these constraints this model can still explain the excess in the M(jj)~120-160 GeV window, as well as the claimed cross section σ(WZ')~4 pb. Implications at the Tevatron would be the associated production of γZ', ZZ', and Z'Z' with the Z'→jj. We show that with tightened jet cuts and improved systematic uncertainties both γZ'→γjj and ZZ'→?(+)?(-) jj channels could be useful to probe this model at the Tevatron. 相似文献
847.
848.
Hongjuan Dong Sau Ha Cheung Yimin Liang Baojiang Wang Rajkumar Ramalingam Ping Wang Hongyan Sun Shuk Han Cheng Yun Wah Lam 《Electrophoresis》2013,34(13):1957-1964
Organelle‐specific cell‐permeable fluorescent dyes are invaluable tools in cell biology as they reveal intracellular dynamics in living cells. Mitrotracker is a family of dyes that strongly label the mitochondrion, a key organelle associated with many crucial cellular functions. Despite the popularity of these dyes, little is known about the molecular mechanism behind their staining specificity. Here, we aimed to identify the protein targets of one member of this dye family, mitotracker red (MTR), by 2DE and MS. MTR bound to cellular proteins covalently, and its fluorescence persisted even after cell lysis, protein solubilization, denaturation, and electrophoresis. This enabled us to display MTR‐labeled proteins by 2DE. The MTR‐specific fluorescent signals on the gel revealed the spots that contained MTR‐conjugated proteins. These spots were analyzed by MS, resulting into the identification of ten proteins. We discovered that one major target is the mitochondrial protein HSP60 and that MTR staining could induce production of HSP60, predisposing cells to heat shock‐like responses. The identification of the molecular targets of biological dyes, or “stainomics,” can help correlate their intracellular staining properties with biochemical affinities. We believe this approach can be applied to a wide range of fluorescent probes. 相似文献
849.
Dr. Amanda G. Jarvis Dr. Petr E. Sehnal Dr. Somia E. Bajwa Dr. Adrian C. Whitwood Dr. Xiangbiao Zhang Man Sing Cheung Prof. Dr. Zhenyang Lin Prof. Dr. Ian J. S. Fairlamb 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(19):6034-6043
A multidentate and flexible diolefin–diphosphine ligand, based on the dibenzylidene acetone core, namely dbaphos ( 1 ), is reported herein. The ligand adopts an array of different geometries at Pt, Pd and Rh. At PtII the dbaphos ligand forms cis‐ and trans‐diphosphine complexes and can be defined as a wide‐angle spanning ligand. 1H NMR spectroscopic analysis shows that the β‐hydrogen of one olefin moiety interacts with the PtII centre (an anagostic interaction), which is supported by DFT calculations. At Pd0 and RhI, the dbaphos ligand exhibits both olefin and phosphine interactions with the metal centres. The Pd0 complex of dbaphos is dinuclear, with bridging diphosphines. The complex exhibits the coordination of one olefin moiety, which is in dynamic exchange (intramolecular) with the other “free” olefin. The Pd0 complex of dbaphos reacts with iodobenzene to afford trans‐[PdII(dbaphos)I(Ph)]. In the case of RhI, dbaphos coordinates to form a structure in which the phosphine and olefin moieties occupy both axial and equatorial sites, which stands in contrast to a related bidentate olefin, phosphine ligand (“Lei” ligand), in which the olefins occupy the equatorial sites and phosphines the axial sites, exclusively. 相似文献
850.
Kwok-Yuen Cheung King-Lung Lee Ka-Leung Lam Tsz-Ying Chan Chi-Wui Lee Chi-Wai Hui 《Journal of Analytical and Applied Pyrolysis》2011,91(1):165-182
Pyrolysis has been extensively studied in past decades as its potential to convert organic wastes into bio-fuels. Pyrolysis is an overall endothermic process but preformed exothermically at its early stage. The overall energy consumption as well as the product quality and yield are affected by the heating rate and the operation temperature. In order to reach its full potential to produce bio-fuels, the energy consumption of the process has to be minimised. An idea to reduce the pyrolysis energy consumption is observed, which suggests trapping the exothermic heat released in the beginning of the pyrolysis process and using it to fulfil the energy requirement of the endothermic reactions at the end of the process. To achieve this, the pyrolysis has to be performed in multiple stages. The operation strategy of the multi-stage pyrolysis, including the number of stages, the operating conditions (e.g. process temperature, heating rate) and residence times of each stages, have to be carefully designed to obtain the most energy saving and the best product yield. The operating strategy of a pyrolysis process therefore greatly depends on the pyrolysis kinetics and the control of heat transfers. Waste tire pyrolysis is chosen as the study example in this paper. The corresponding reaction kinetics at different heating rates are investigated via experiments. Based on the experimental results, a mathematical model integrating kinetics and heat transfers is then developed. The objective of the model is to design a suitable operation strategy for the multi-stage pyrolysis process. A four-stage strategy is finally proposed for the tire pyrolysis, which has the sequence of heating, adiabatic, heating and adiabatic. The strategy is verified by the model, and it is capable to save about 22.5% energy consumption compared to the conventional strategy. 相似文献