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排序方式: 共有318条查询结果,搜索用时 31 毫秒
41.
This paper presents Hurst exponent footprints from pseudo-dynamic measurements of significantly varied activities on a damaged bridge structure during rehabilitation through continuous monitoring. The system is interesting due to associated uncertainty in large-scale structures and significant presence of human intervention arising from fundamentally different processes. Investigations into the variation of computed Hurst exponents on time series of limited lengths are carried out in this regard. The Hurst exponents are compared with respect to specific events during the rehabilitation, as well as with the data collection locations. The variations of local Hurst exponents about the values computed for each activity are presented. The scaling of Hurst exponents for different activities is also investigated; these are representative of the extent of multifractality for each event. The extent of multifractality is assessed along with its source and time dependency. 相似文献
42.
Mark T. Sims Laurence C. Abbott Robert M. Richardson John W. Goodby 《Liquid crystals》2019,46(1):11-24
An assessment of the data processing and analysis methods used to obtain the second- and fourth-rank orientational order parameters of liquid crystals from X-ray scattering experiments has been carried out, using experimental data from four extensively studied alkyl-cyanobiphenyls and calculated data generated from two general types of theoretical orientational distribution function. The application of a background subtraction and two different baseline correction methods to the scattering profiles is assessed, along with three different methods to analyse the processed data. The choice of baseline correction method is shown to have a significant effect: an offset to zero overestimates the order parameters from the experimental and calculated data sets, particularly for lower order parameters arising from broad distributions, whereas an offset to a value estimated from regions of low scattering intensity provides experimental values close to those reported from other experimental techniques. By contrast, the three different analysis methods are shown generally to result in relatively small absolute differences between the order parameters. We outline a straightforward general approach to experimental X-ray scattering data processing and analysis for uniaxial phases that results in order parameters that match well with those reported using other experimental techniques. 相似文献
43.
We show that the equilibrium distribution for the dimer process on the finite Cayley tree tends to a translation invariant
limit as the size of the tree tends to infinity. The same is true for the blocking process except when there is a phase transition,
in which case there are two limits, each a one-step translation of the other. We also find correlations for occupation probabilities. 相似文献
44.
45.
D. J. Sims W. S. Andrews X. Wang K. A. M. Creber 《Journal of Radioanalytical and Nuclear Chemistry》2008,277(1):137-142
In 1951, unsaturated prairie soil was contaminated with fission products and actinides. Fifty years later, in 2001, soil samples
were collected from the contaminated site. This paper describes the techniques used to analyze these samples, including gamma-spectroscopy
(GS) for 137Cs, neutron activation analysis (NAA/GS) for 238U, liquid scintillation counting (LSC) for 90Sr and inductively coupled plasma mass spectroscopy (ICP-MS) for 238U and 113mCd. As expected, ICP-MS was found to have the lowest detection level, while the techniques were ranked in order of increasing
uncertainty as GS, NAA/GS, ICP-MS and LSC. 相似文献
46.
Aidan Rafferty Dr. Michael J. Morten Dr. John M. Gardiner Dr. Steven W. Magennis 《Chemphyschem》2016,17(21):3442-3446
The first single‐molecule fluorescence detection of a structurally‐defined synthetic carbohydrate is reported: a heparan sulfate (HS) disaccharide fragment labeled with Alexa488. Single molecules have been measured whilst freely diffusing in solution and controlled encapsulation in surface‐tethered lipid vesicles has allowed extended observations of carbohydrate molecules down to the single‐molecule level. The diverse and dynamic nature of HS–protein interactions means that new tools to investigate pure HS fragments at the molecular level would significantly enhance our understanding of HS. This work is a proof‐of‐principle demonstration of the feasibility of single‐molecule studies of synthetic carbohydrates which offers a new approach to the study of pure glycosaminoglycan (GAG) fragments. 相似文献
47.
A series of catalysts have been prepared for use in the asymmetric transfer hydrogenation of ketones. The complexes were prepared using a [4 + 2] cycloaddition reaction at a key step in the reaction sequence. This provides a means for the synthesis of catalysts with modifications at specific sites. 相似文献
48.
Phosphatidyl inositol 4,5-bisphosphate (PIP2) and phosphatidyl inositol 3,4,5-trisphosphate (PIP3) labeled with 4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-propionic acid (BODIPY FL) on the acyl chain or a phosphatidyl ethanolamine head group were separated by CE with LIF detection. Several methods and capillary-coating procedures were tested for the separation of these phosphatidyl inositol phosphates (PIPs) at 20 degrees C. Separation of the PIPs in less than 20 min with excellent resolution was achieved using a buffer containing sodium deoxycholate (SDC), 1-propanol, MgCl2 and the polymer coating reagent, EOTrol LR. The efficiency of the optimized method was as high as 1.3x10(5) plates. The dependence of the separation on the concentration of 1-propanol, SDC, and MgCl2 was determined. The separation of PIP2 and PIP3 was primarily due to differential binding of the lipids to Mg2+ rather than to different solubilities in the micellar phase. The role of the SDC was to prevent adsorption of the hydrophobic lipids to the capillary wall and thus enhance the efficiency. The fluorescent PIPs are of value for both in vitro and in vivo assays of phospholipid metabolism. In particular, the use of these lipids with the optimized capillary-based separation will be of utility for drug screening as well as cell-based assays. 相似文献
49.
This paper investigates the design and analysis of a novel energy harvesting device that uses magnetic levitation to produce an oscillator with a tunable resonance. The governing equations for the mechanical and electrical domains are derived to show the designed system reduces to the form of a Duffing oscillator under both static and dynamic loads. Thus, nonlinear analyses are required to investigate the energy harvesting potential of this prototypical nonlinear system. Theoretical investigations are followed by a series of experimental tests that validate the response predictions. The motivating hypothesis for the current work was that nonlinear phenomenon could be exploited to improve the effectiveness of energy harvesting devices. 相似文献
50.
Aidan R. McDonald 《Journal of organometallic chemistry》2009,694(14):2153-2759
We present the synthesis, via Adler condensation reactions, of mono- and tetrakis-4-(ethynyl-phenyl)porphyrin ligands and the zinc and manganese complexes thereof. The formed complexes were immobilised on silica by reacting the ethynyl groups with azide-functionalised silica in a copper(I) catalysed Huisgens 1,3-dipolar cycloaddition reaction. The synthesised metallo-porphyrin containing materials were thoroughly characterised using various solid-state techniques (NMR, IR, UV-Vis, elemental content analysis). The manganese containing materials were applied as catalysts in the epoxidation of various alkenes (cyclooctene, cyclohexene, styrene) with various oxidants (iodosylbenzene, tert-butylperoxide). The heterogenised homogeneous catalysts show diminished activity and yields compared to the analogous homogeneous catalysts (71% yield cf. 92% for cyclooctene epoxidation, TOF 82 h−1 cf. 230 h−1). Upon recycling, the heterogenised catalysts become gradually less active over five cycles until they are catalytically inactive. The deactivation process is discussed, with spectroscopy suggesting that the catalysts themselves are intact and thus stable to the reaction conditions and recycling, however there is likely some decomplexation, and also both chemical and mechanical decomposition of the silica support resulting in inaccessibility to the catalytic site. 相似文献