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991.
N. R. Larsen 《Journal of Radioanalytical and Nuclear Chemistry》1979,52(1):85-91
Neodymium is separated from solutions of spent nuclear fuel by high-pressure liquid chromatography in methanol-nitric acid-water media using an anion-exchange column. Chromatograms obtained by monitoring at 280 nm, illustrate the difficulties especially with the fission product ruthenium in nuclear chemistry. Preseparation of the rare earths and trivalent actinides using a di(2-ethylhexyl)phosphoric acid/kieselguhr column is described. 相似文献
992.
P.K. Larsen J.F. van der Veen A. Mazur J. Pollmann B.H. Verbeek 《Solid State Communications》1981,40(4):459-462
Angle-resolved photoemission measurements for GaAs(001) prepared by MBE have been carried out using synchroton radiation. Observed bulk features in the spectra can be explained by a direct transition model using free-electron-like final states down to energies as low as 16 eV above the top of the valence bands. Spectral bulk valence band features can be distinguished from surface features by an appropriate choice of photon energies and polar angles. This is demonstrated using calculated valence bands. 相似文献
993.
994.
[reaction: see text]. Catalysis of the glyoxylate-ene reaction by dicationic P2Pt(II) complexes is subject to anion-dependent additive effects. For [((S)-MeOBiphep)Pt](OTf)2 catalysts, acidic phenols such as 3-CF3-C6H3OH or C6F5OH provide substantial rate increases but do not affect the more active SbF6-based catalysts. Enantioselectivity and reactivity also increased with diphosphine basicity, with 4-t-Bu-substituted MeOBiphep ligands yielding the highest enantioselectivities. 相似文献
995.
From the very beginning organic chemistry and total synthesis have been intimately joined. In fact, one of the first things that freshmen in organic chemistry learn is how to join two molecules together to obtain a more complex one. Of course they still have a long way to go to become fully mature synthetic chemists, but they must have the primary instinct to build molecules, as synthesis is the essence of organic chemistry. With the different points of view that actually coexist in the chemical community about the maturity of the science (art, or both) of organic synthesis, it is clear that nowadays we know how to make almost all of the most complex molecules ever isolated. The primary question is how easy is it to accomplish? For the readers of papers describing the total synthesis of either simple or complex molecules, it appears that the routes followed are, most of the time, smooth and free of troubles. The synthetic scheme written on paper is, apparently, done in the laboratory with few, if any, modifications and these, essentially, seem to be based on finding the optimal experimental conditions to effect the desired reaction. Failures in the planned synthetic scheme to achieve the goal, detours imposed by unexpected reactivity, or the absence of reactivity are almost never discussed, since they may diminish the value of the work reported. This review attempts to look at total synthesis from a different side; it will focus on troubles found during the synthetic work that cause detours from the original synthetic plan, or on the dead ends that eventually may force redesign. From there, the evolution from the original route to the final successful one that achieves the synthetic target will be presented. The syntheses discussed in this paper have been selected because they contain explicit information about the failures of the original synthetic plan, together with the evolution of the final route to the target molecule. Therefore, they contain a lot of useful negative information that may otherwise be lost. 相似文献
996.
This paper is motivated by our experiences since 1990 with developing system simulation models to help UK companies in the restructured electricity industry understand the radically different market within which they must become competitive. When public utilities such as electricity have been restructured, deregulated and/or privatised, the process has often been associated with a major change in the competitive environment. As a consequence, the strategic and regulatory uncertainties ahead for these companies are unprecedented. In such a market there has been no historical evolution and all the participants including the regulatory institutions have very little understanding of how it will operate in the short term and evolve in the future. In this situation, the use of system dynamic models appears to offer an attractive way of gaining insights into how aspects of the competitive market might evolve. In the absence of real experience and relevant analogies, learning from models assumes a key role. Such models cannot be validated empirically, but can be developed to represent how the system is designed to operate. From such a prototypical basis, sensitivity analysis can generate insights on the strategic opportunities created by failings in the market design, or its potential instability to shocks and market imperfections. 相似文献
997.
The numerical solution of a possible inconsistent system oflinear inequalities in the l1 sense is considered. The non-differentiablel1 norm minimization problem is approximated by a piecewisequadratic Huber smooth function. A continuation algorithm isdesigned to find an l1 solution of the inequality system. Inthe case where the linear inequality system is consistent, asolution is obtained by solving any smoothed problem. Otherwise,the algorithm is shown to terminate in a finite number of iterations.We also consider an alternative smoothing scheme which sharessimilar properties with the first one, but results in an improvedcomputational performance of the continuation algorithm on inconsistentsystems. Numerical experiments are conducted to test the efficiencyof the algorithm. 相似文献
998.
999.
1000.
Age Larsen 《Zeitschrift fur Physik C Particles and Fields》1983,16(3):259-262
Using parity violating nucleon wave function effects we make predictions for spin asymmetries inpp and \(\bar p\) p scattering at moderate and high energies 相似文献