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A new method for refinement of 3D molecular structures by geometry optimization is presented. Prerequisites are a force field and a very fast procedure for the calculation of chemical shifts in every step of optimization. To the energy, provided by the force field (COSMOS force field), a pseudoenergy, depending on the difference between experimental and calculated chemical shifts, is added. In addition to the energy gradients, pseudoforces are computed. This requires the derivatives of the chemical shifts with respect to the coordinates. The pseudoforces are analytically derived from the integral expressions of the bond polarization theory. Single chemical shift values attributed to corresponding atoms are considered for structural correction. As a first example, this method is applied for proton position refinement of the D-mannitol X-ray structure. A crystal structure refinement with 13C chemical shift pseudoforces is carried out. 相似文献
3.
The motion of a holonomic scleronomic non-conservative mechanicalsystem with minimal dissipation is considered. As applicationsof the theory several problems are studied in detail. 相似文献
4.
A Mukherjee M Dasgupta DJ Hinde CR Morton AC Berriman RD Butt JO Newton H Timmers 《Pramana》2001,57(1):195-198
Fusion cross-sections for the 7Li + 12C reaction have been measured at energies above the Coulomb barrier by the direct detection of evaporation residues. The heavy
evaporation residues with energies below 3 MeV could not be separated out from the α-particles in the spectrum and hence their
contribution was estimated using statistical model calculations. The present work indicates that suppression of fusion cross-sections
due to the breakup of 7Li may not be significant for 7Li + 12C reaction at energies around the barrier. 相似文献
5.
The kinetics of the gas‐phase reactions of O3 with a series of selected terpenes has been investigated under flow‐tube conditions at a pressure of 100 mbar synthetic air at 295 ± 0.5 K. In the presence of a large excess of m‐xylene as an OH radical scavenger, rate coefficients k(O3+terpene) were obtained with a relative rate technique, (unit: cm3 molecule?1 s?1, errors represent 2σ): α‐pinene: (1.1 ± 0.2) × 10?16, 3Δ‐carene: (5.9 ± 1.0) × 10?17, limonene: (2.5 ± 0.3) × 10?16, myrcene: (4.8 ± 0.6) × 10?16, trans‐ocimene: (5.5 ± 0.8) × 10?16, terpinolene: (1.6 ± 0.4) × 10?15 and α‐terpinene: (1.5 ± 0.4) × 10?14. Absolute rate coefficients for the reaction of O3 with the used reference substances (2‐methyl‐2‐butene and 2,3‐dimethyl‐2‐butene) were measured in a stopped‐flow system at a pressure of 500 mbar synthetic air at 295 ± 2 K using FT‐IR spectroscopy, (unit: cm3 molecule?1 s?1, errors represent 2σ ): 2‐methyl‐2‐butene: (4.1 ± 0.5) × 10?16 and 2,3‐dimethyl‐2‐butene: (1.0 ± 0.2) × 10?15. In addition, OH radical yields were found to be 0.47 ± 0.04 for 2‐methyl‐2‐butene and 0.77 ± 0.04 for 2,3‐dimethyl‐2‐butene. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 394–403, 2002 相似文献
6.
A new, vectorial approach to fast correlation attacks on binary memoryless combiners is proposed. Instead of individual input sequences or their linear combinations, the new attack is targeting subsets of input sequences as a whole thus exploiting the full correlation between the chosen subset and the output sequence. In particular, the set of all the input sequences can be chosen as the target. The attack is based on a novel iterative probabilistic algorithm which is also applicable to general memoryless combiners over finite fields or finite rings. To illustrate the effectiveness of the introduced approach, experimental results obtained for random balanced combining functions are presentedMost of this work was done while he was with Rome CryptoDesign Center, Gemplus, Italy 相似文献
7.
Dürr UH Grage SL Witter R Ulrich AS 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2008,191(1):7-15
Structural parameters of peptides and proteins in biomembranes can be directly measured by solid state NMR of selectively labeled amino acids. The 19F nucleus is a promising label to overcome the low sensitivity of 2H, 13C or 15N, and to serve as a background-free reporter group in biological compounds. To make the advantages of solid state 19F NMR fully available for structural studies of polypeptides, we have systematically measured the chemical shift anisotropies and relaxation properties of the most relevant aromatic and aliphatic 19F-labeled amino acids. In this first part of two consecutive contributions, six different 19F-substituents on representative aromatic side chains were characterized as polycrystalline powders by static and MAS experiments. The data are also compared with results on the same amino acids incorporated in synthetic peptides. The spectra show a wide variety of lineshapes, from which the principal values of the CSA tensors were extracted. In addition, temperature-dependent T(1) and T(2) relaxation times were determined by 19F NMR in the solid state, and isotropic chemical shifts and scalar couplings were obtained in solution. 相似文献
8.
9.
Hesse-Ertelt S Witter R Ulrich AS Kondo T Heinze T 《Magnetic resonance in chemistry : MRC》2008,46(11):1030-1036
Solid-state (13)C-NMR spectroscopy was used to characterize native cellulose pellicles from two strains of Gluconacetobacter xylinus (ATCC 53582, ATCC 23769), which had been statically cultivated in Hestrin-Schramm (HS) medium containing fully (13)C-labeled beta-D-glucose-U-(13)C(6) as the sole source of carbon. For both samples, the (13)C-NMR chemical shifts were completely assigned for each (13)C-labeled site of cellulose I(alpha) with the aid of 2D refocused INADEQUATE NMR. To determine the principal chemical shift tensor components, a pulse sequence based on the recoupling of anisotropy information (RAI) was applied at 10 kHz MAS. The detailed (13)C tensors of cellulose I(alpha) from different bacterial celluloses are thus available now for the first time, and these results have been compared with previously published data of nonenriched material and with theoretical predictions. 相似文献
10.