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111.
Currently, the most efficient passive attack on the NTRU public-key cryptosystem, proposed by Coppersmith and Shamir [1], is based on finding a short enough vector in an integral lattice. An NTRU lattice possesses a cyclic automorphism group whose symmetry may be exploited. We have designed methods for reducing bases of NTRU integral lattices based on this symmetry. In addition to these methods, we use hill-descending techniques to combine new and proposed lattice-reduction algorithms. This approach includes deterministic and non-deterministic components which may be efficiently parallelized. 相似文献
112.
113.
Herbert Hutter Peter Wilhartitz Manfred Grasserbauer 《Fresenius' Journal of Analytical Chemistry》1993,346(1-3):66-68
Summary The potential of 3D-SIMS for characterization of high molybdenum powder and sintered high purity molybdenum will be demonstrated. The concentration of the measured trace elements in the sintered molybdenum did not exceed 200 ppb. In the powder the concentration was found to be about 1 ppm. For material scientists it is very important to ascertain if the trace elements are homogeneously distributed or precipitated. Although the concentration of the elements of interest was rather low, qualitative images of the three dimensional distribution can be obtained. 相似文献
114.
115.
Hutter H Brunner C Nikolov S Mittermayer C Grasserbauer M 《Analytical and bioanalytical chemistry》1996,355(5-6):585-590
Secondary ion mass spectrometry (SIMS) exhibits a unique potential for the measurement of two-and three-dimensional distributions of trace elements in advanced materials, which is demonstrated on relevant technological problems. One example is the characterization of high purity iron. With this material segregation experiments have been performed and the initial and final distribution of the trace elements have been measured. Another example is the investigation of the corrosion behaviour of high purity chromium. Samples oxidized with (16)O and (18)O have been measured to explain the growing and adhesion of the oxide layer. All imaging techniques generate a vast quantitiy of data. In order to extract the important information the assistance of chemometric tools is essential. Detection of chemical phases by classification using neural networks or de-noising of scanning-SIMS images by wavelet-filtering demonstrates the increase of the performance of analytical imaging techniques. 相似文献
116.
Reiher M Kirchner B Hutter J Sellmann D Hess BA 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(18):4443-4453
A general photochemical activation process of inert dinitrogen coordinated to two metal centers is presented on the basis of high-level DFT and ab initio calculations. The central feature of this activation process is the occupation of an antibonding pi* orbital upon electronic excitation from the singlet ground state S0 to the first excited singlet state S1. Populating the antibonding LUMO weakens the triple bond of dinitrogen. After a vertical excitation, the excited complex may structurally relax in the S1 state and approaches its minimum structure in the S1 state. This excited-state minimum structure features the dinitrogen bound in a diazenoid form, which exhibits a double bond and two lone pairs localized at the two nitrogen atoms, ready to be protonated. Reduction and de-excitation then yield the corresponding diazene complex; its generation represents the essential step in a nitrogen fixation and reduction protocol. The consecutive process of excitation, protonation, and reduction may be rearranged in any experimentally appropriate order. The protons needed for the reaction from dinitrogen to diazene can be provided by the ligand sphere of the complexes, which contains sulfur atoms acting as proton acceptors. These protonated thiolate functionalities bring protons close to the dinitrogen moiety. Because protonation does not change the pi*-antibonding character of the LUMO, the universal and well-directed character of the photochemical activation process makes it possible to protonate the dinitrogen complex before it is irradiated. The pi*-antibonding LUMO plays the central role in the activation process, since the diazenoid structure was obtained by excitation from various occupied orbitals as well as by a direct two-electron reduction (without photochemical activation) of the complex; that is, the important bending of N2 towards a diazenoid conformation can be achieved by populating the pi*-antibonding LUMO. 相似文献
117.
FeII4L6 tetrahedral cage 1 was prepared from a redox-active dicationic naphthalenediimide (NDI) ligand. The +20 charge of the cage makes it a good host for anionic guests, with no binding observed for neutral aromatic molecules. Following reduction by Cp2Co, the cage released anionic guests; subsequent oxidation by AgNTf2 led to re-uptake of anions. In its reduced form, however, 1 was observed to bind neutral C60. The fullerene guest was subsequently ejected following cage re-oxidation. The guest release process was found to be facilitated by anion-mediated transport from organic to aqueous solution. Cage 1 thus employs electron transfer as a stimulus to control the uptake and release of both neutral and charged guests, through distinct pathways.FeII4L6 cage 1 binds anionic guests but not neutral guests. In its reduced form, the cage can bind neutral C60. Reduction and oxidation of the cage could thus be used as a stimulus to control the uptake and release of both neutral and charged guests. 相似文献
118.
Simultaneous quantification of total medium- and long-chain fatty acids in human milk by capillary gas chromatography with split injection 总被引:2,自引:0,他引:2
G van der Steege F A Muskiet I A Martini N H Hutter E R Boersma 《Journal of chromatography. A》1987,415(1):1-11
Four different quantification methods for the capillary gas chromatographic determination of medium-chain fatty acids (6:0-12:0) and myristic acid in human milk samples, using a split injector, were compared. Odd-carbon-numbered fatty acids (5:0-17:0) were added as internal standards. Each medium-chain fatty acid and myristic acid was calculated on the basis of: the peak area of the internal standard with one methylene group less; the peak area of the internal standard with one methylene group more; half the sum of the peak areas of the internal standards with one methylene group less and more (bracketting method); the peak area of 17:0. The peak-area ratio of each analyte and 17:0 in a standard was found to be subject to an unacceptably high coefficient of variation. From the methods using internal standards with one methylene group more and less, the bracketting method was found to be the best, resulting in recoveries close to 100%, with the lowest coefficients of variation. The method was applied for the determination of the fatty acid composition of mature milk samples of 47 Cura?aoan women. 相似文献
119.
Kelly T Bossoutrot V Magneron I Wirtz K Treacy J Mellouki A Sidebottom H Le Bras G 《The journal of physical chemistry. A》2005,109(2):347-355
Product distribution studies of the OH radical and Cl atom initiated oxidation of CF3CH2CH2OH in air at 1 atm and 298 +/- 5 K have been carried out in laboratory and outdoor atmospheric simulation chambers in the presence and absence of NOx. The results show that CF3CH2CHO is the only primary product and that the aldehyde is fairly rapidly removed from the system. In the absence of NOx the major degradation product of CF3CH2CHO is CF3CHO, and the combined yields of the two aldehydes formed from CF3CH2CH2OH are close to unity (0.95 +/- 0.05). In the presence of NOx small amounts of CF3CH2C(O)O2NO2 were also observed (<15%). At longer reaction times CF3CHO is removed from the system to give mainly CF2O. The laser photolysis-laser induced fluorescence technique was used to determine values of k(OH + CF3CH2CH2OH) = (0.89 +/- 0.03) x 10(-12) and k(OH + CF3CH2CHO) = (2.96 +/- 0.04) x 10(-12) cm3 molecule(-1) s(-1). A relative rate method has been employed to measure the rate coefficients k(OH + CF3CH2CH2OH) = (1.08 +/- 0.05) x 10(-12), k(OH + C6F13CH2CH2OH) = (0.79 +/- 0.08) x 10(-12), k(Cl + CF3CH2CH2OH) = (22.4 +/- 0.4) x 10(-12), and k(Cl + CF3CH2CHO) = (25.7 +/- 0.4) x 10(-12) cm3 molecule(-1) s(-1). The results from this investigation are discussed in terms of the possible importance of emissions of fluorinated alcohols as a source of fluorinated carboxylic acids in the environment. 相似文献
120.
Guhados G Wan W Hutter JL 《Langmuir : the ACS journal of surfaces and colloids》2005,21(14):6642-6646
The ability of the atomic force microscope to measure forces with subnanonewton sensitivity at nanometer-scale lateral resolutions has led to its use in the mechanical characterization of nanomaterials. Recent studies have shown that the atomic force microscope can be used to measure the elastic moduli of suspended fibers by performing a nanoscale three-point bending test, in which the center of the fiber is deflected by a known force. We extend this technique by modeling the deflection measured at several points along a suspended fiber, allowing us to obtain more accurate data, as well as to justify the mechanical model used. As a demonstration, we have measured a value of 78 +/- 17 GPa for Young's modulus of bacterial cellulose fibers with diameters ranging from 35 to 90 nm. This value is considerably higher than previous estimates, obtained by less direct means, of the mechanical strength of individual cellulose fibers. 相似文献