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61.
T-junctions are common elements in flow duct networks. It is shown that for low Strouhal numbers, based on the duct diameter, their acoustic scattering properties can be described using an incompressible quasi-steady model. Models are derived for systems subjected to combinations of grazing and bias mean flow, and are shown to work in both the limiting cases—that is, grazing or bias flow alone—as well as for the joining or dividing flow configurations. The upper Strouhal number for which the quasi-steady models are applicable is limited by flow-acoustic interaction effects, which differ significantly between the different flow configurations. Generally the models are applicable up to Strouhal numbers of approximately 0.1-0.2, which is comparable with previous published models for other configurations such as bends and orifices. This range is sufficient to make the model useful in many important engineering applications. 相似文献
62.
W. H. Bennett W. I. H. Moll H. C. Burger H. F. Mullikin J. A. Campbell J. H. Hibben A. Beck W. K. Hutchison K. A. Kobe S. Pexton E. J. Arveson Fr. Strieck Ch. W. Wilson W. Ackermann O. Pfundt Y. Kauko W. Mc K. Martin J. R. Green M. Kleiber H. Briese E. Biesalski H. Giehmann M. Mugdan J. Sixt R. Ruyssen N. Allen G. Denigès F. W. Horst L. Benoist H. Tramm W. Grimme P. Schuftan H. Tropsch R. Kassler W. Deckert M. Konschak C. Aßmann L. E. Karlsson H. L. Cupples W. Klempt W. Riese J. H. Bruun M. M. Hicks-Bruun E. C. Mathis 《Analytical and bioanalytical chemistry》1934,96(9-10):336-346
63.
Elin S. Karlsson Caroline H. Johnson Sunil Sarda Lisa Iddon Mazhar Iqbal Xiaoli Meng John R. Harding Andrew V. Stachulski Jeremy K. Nicholson Ian D. Wilson John C. Lindon 《Rapid communications in mass spectrometry : RCM》2010,24(20):3043-3051
The use of high‐performance liquid chromatography/mass spectrometry (HPLC/MS) and proton nuclear magnetic resonance (1H NMR) spectroscopy for the kinetic analysis of acyl glucuronide (AG) isomerisation and hydrolysis of the 1‐β‐O‐acyl glucuronides (1‐β‐O‐AG) of phenylacetic acid, (R)‐ and (S)‐α‐methylphenylacetic acid and α,α‐dimethylphenylacetic acid is described and compared. Each AG was incubated in both aqueous buffer, at pH 7.4, and control human plasma at 37°C. Aliquots of these incubations, taken throughout the reaction time‐course, were analysed by HPLC/MS and 1H NMR spectroscopy. In buffer, transacylation reactions predominated, with relatively little hydrolysis to the free aglycone observed. In human plasma incubations the calculated rates of reaction were much faster than for buffer and, in contrast to the observations in buffer, hydrolysis to the free aglycone was a significant contributor to the overall reaction. A diagnostic analytical methodology based on differential mass spectrometric fragmentation of 1‐β‐O‐AGs compared to the 2‐, 3‐ and 4‐positional isomers, which enables selective determination of the former, was confirmed and applied. These findings show that HPLC/MS offers a viable alternative to the more commonly used NMR spectroscopic approach for the determination of the transacylation and hydrolysis reactions of these AGs, with the major advantage of having the capability to do so in a complex biological matrix such as plasma. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
64.
Positive muons have been used to monitor the proton and deuteron mobilities in mixed, concentrated NbH_xD_y hydrides, with
x+y= constant. The mobility of the muons decreases linearly with increasing D‐content, which is expected if the protons and
the deuterons move in an uncorrelated fashion. Combined with other evidence which suggests that such correlations exist, the
present observation may be interpreted as due to a destruction of a correlated motion of H’s or D’s in the vicinity of the
muons.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
65.
Analysis of mucosal mucins separated by SDS-urea agarose polyacrylamide composite gel electrophoresis 总被引:1,自引:0,他引:1
Efficient separation of mucins (200 kDa-2 MDa) was demonstrated using gradient SDS agarose/polyacrylamide composite gel electrophoresis (SDS-AgPAGE). Inclusion of urea (SDS-UAgPAGE) in the gels casting were shown to have no effect on the migration of mucins in the gel and allowed casting of gel at room temperature. This simplified the procedure for multiple casting of agarose polyacrylamide gradients and increased reproducibility of these gels. Hence, the implementation of urea makes the technique applicable for high throughput isolation and screening of mucin oligosaccharides by LC-MS after releasing the oligosaccharides from isolated, blotted mucin subpopulations. It was also shown that the urea addition had no effect on other supporting applications such as western and lectin blotting. In addition, identification of the mucin protein after tryptic digestion and LC-MS was possible and no protein carbamylation due to the presence of urea in the gel was detected. LC-MS software developed for metabolomic analysis was used for O-linked oligosaccharide detection and differential display of various mucin samples. Using this method, heterogeneous glycosylation of mucins and mucin-type molecules isolated by SDS-AgPAGE and SDS-UAgPAGE was shown to consist of more than 80 different components in a single band, and in the extreme cases, up to 300-500 components (MUC5B/AC from saliva and sputum and). Metabolomic software was also used to show that the migration of mucin isoforms within the gel is due to heterogeneous size distribution of the oligosaccharides, with the slower migrating bands enriched in high-molecular-weight oligosaccharides. 相似文献
66.
Verho O Johnston EV Karlsson E Bäckvall JE 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(40):11216-11222
The synthesis of a new series of cyclopentadienylruthenium catalysts with varying electronic properties and their application in racemization of secondary alcohols are described. These racemizations involve two key steps: 1) β-hydride elimination (dehydrogenation) and 2) re-addition of the hydride to the intermediate ketone. The results obtained confirm our previous theory that the electronic properties of the substrate determine which of these two steps is rate determining. For an electron-deficient alcohol the rate-determining step is the β-hydride elimination (dehydrogenation), whereas for an electron-rich alcohol the re-addition of the hydride becomes the rate-determining step. By matching the electronic properties of the catalyst with the electronic properties of the alcohol, we have now shown that a dramatic increase in racemization rate can be obtained. For example, electron-deficient alcohol 15 racemized 30 times faster with electron-deficient catalyst 6 than with the unmodified standard catalyst 4. The application of these protocols will extend the scope of cyclopentadienylruthenium catalysts in racemization and dynamic kinetic resolution. 相似文献
67.
Wiklander J Karlsson BC Aastrup T Nicholls IA 《Analytical and bioanalytical chemistry》2011,400(5):1397-1404
A series of streptavidin-mimicking molecularly imprinted polymers has been developed and evaluated for their biotin binding characteristics. A combination of molecular dynamics and NMR spectroscopy was used to examine potential polymer systems, in particular with the functional monomers methacrylic acid and 2-acrylamidopyridine. The synthesis of copolymers of ethylene dimethacrylate and one or both of these functional monomers was performed. A combination of radioligand binding studies and surface area analyses demonstrated the presence of selectivity in polymers prepared using methacrylic acid as the functional monomer. This was predicted by the molecular dynamics studies showing the power of this methodology as a prognostic tool for predicting the behavior of molecularly imprinted polymers.
The biotin binding characteristics of a series of molecularly imprinted polymers have been evaluated and correlated to predictions made by molecular dynamics simulations and 1H-NMR titrations 相似文献
68.
69.
Ek M Borgstr?m MT Karlsson LS Hetherington CJ Wallenberg LR 《Microscopy and microanalysis》2011,17(5):752-758
The twin interface structure in twinning superlattice InP nanowires with zincblende structure has been investigated using electron exit wavefunction restoration from focal series images recorded on an aberration-corrected transmission electron microscope. By comparing the exit wavefunction phase with simulations from model structures, it was possible to determine the twin structure to be the ortho type with preserved In-P bonding order across the interface. The bending of the thin nanowires away from the intended 110 axis could be estimated locally from the calculated diffraction pattern, and this parameter was successfully taken into account in the simulations. 相似文献
70.
Martin Månsson Oscar Tjernberg Tomas Claesson Henrik S. Karlsson Ulf O. Karlsson 《Applied Surface Science》2006,252(15):5308-5311
Transiently excited electron states at the GaSb(0 0 1) surface have been studied by means of time- and angle-resolved photoemission spectroscopy based on a femtosecond laser system. A normally unpopulated surface electron state has been found at ∼250 meV above the valence band maximum with a strong confinement at the center of the surface Brillouin zone. The lifetime of transiently excited carriers at the intergap surface states has been found to be ∼11 ps, associated with rapid carrier diffusion. 相似文献