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The paper presents an improved reversed-phase LC method for the separation of the pigments from green leaves. A good separation of carotenoids and of their cis- and trans-isomers was achieved, especially for the separation of trans-lutein, zeaxanthin, cis-lutein, which are usually not well separated. No perfect separation of alpha-carotene, beta-carotene and pheophytin a was possible, but conditions for a perfect coelution of pheophytin a with either beta-carotene or alpha-carotene were established. Simultaneous equations allowing the determination of pheophytin a and alpha-carotene or pheophytin a and beta-carotene are also given. 相似文献
4.
We report six-dimensional quantum dynamics calculations of the dissociative scattering of molecular hydrogen from the copper111 surface. Two potential energy surfaces are investigated and the results are compared with experiment. Our study completes the preliminary work of Somers et al. [Chem. Phys. Lett. 360, 390 (2002)] and focuses on the role of initial vibrational excitation and on isotopic effects. None of the two investigated potential energy surfaces is found satisfactory: the use of neither potential yields reaction and vibrational excitation probabilities and vibrational efficacies that are in close agreement with experiment. In addition to showing the shortcomings of existing potential energy surfaces we point out an inconsistency in the experimental fits for D2. 相似文献
5.
P. Lemoine S.S. Roy J.P. Quinn P.D. Maguire J.A.D. McLaughlin 《Applied Physics A: Materials Science & Processing》2007,86(4):451-456
We present a comparative study where carbon nanostructures were prepared by electron and ion beam methods. Thin films of 10×10 μm2 area were prepared and analysed by Raman analysis, nanoindentation, energy dispersive X-ray analysis (EDX) and atomic force
microscopy (AFM). The material formed is not soft and graphitic, but of intermediate hardness (6–13 GPa) and with Raman spectral
features similar to those of hydrogenated amorphous carbon, although it contains a significant Ga content (up to 25 at. %).
This study was used to form sharp AFM supertip structures which were used to image sintered ceramic samples and films of aligned
carbon nanotubes. Compared to traditional Si tips, this gave an improved rendering of the sample’s aspect ratio although the
resolution is limited by the diameter of the C supertips.
PACS 81.05.Uw; 81.07.-b; 78.30.-j 相似文献
6.
In this work, we extracted the film's hardness (HF) of ultra-thin diamond-like carbon layers by simultaneously taking into account the tip blunting and the substrate effect. As compared to previous approaches, which did not consider tip blunting, this resulted in marked differences (30-100%) for the HF value of the thinner carbon coatings. We find that the nature of the substrate influences this intrinsic film parameter and hence the growth mechanisms. Moreover, the HF values generally increase with film thickness. The 10 nm and 50 nm thick hydrogenated amorphous carbon (a-C:H) films deposited onto Si have HF values of, respectively, ∼26 GPa and ∼31 GPa whereas the 10 nm and 50 nm thick tetrahedral amorphous carbon (t-aC) films deposited onto Si have HF values of, respectively, ∼29 GPa and ∼38 GPa. Both the a-C:H and t-aC materials also show higher density and refractive index values for the thicker coatings, as measured, respectively by X-ray reflectometry and optical profilometry analysis. However, the Raman analysis of the a-C:H samples show bonding characteristics which are independent of the film thickness. This indicates that in these ultra-thin hydrogenated carbon films, the arrangement of sp2 clusters does not relate directly to the hardness of the film. 相似文献
7.
De Winter J Lemaur V Ballivian R Chirot F Coulembier O Antoine R Lemoine J Cornil J Dubois P Dugourd P Gerbaux P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(35):9738-9745
Ion mobility spectrometry coupled with mass spectrometry was used to experimentally determine the three-dimensional structure of multiply charged sodium cationized polylactides (PLA). In particular, the experiments were conducted to evaluate the influence of the charge state and the size on the gas-phase conformation of cationized PLA. The measured collision cross sections were then compared to calculated values obtained by computational chemistry methods. The most striking feature was the experimental and theoretical observation of a breaking point in the quasilinear relationship between the average collision cross sections and the number of monomer units for the triply charged cations. This breaking point was theoretically demonstrated, for the doubly and triply charged cations, to be associated with a significant folding of the polymer chains around the cationizing agents. The occurrence of such breaking points could be exploited to correlate the charge state of the most intense ion series observed upon electrospray ionization with the number-average molecular mass of a polymer. 相似文献
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Vincent Larraillet Aleksey Vorobyev Claire Brunet Jér?me Lemoine Yury O. Tsybin Rodolphe Antoine Philippe Dugourd 《Journal of the American Society for Mass Spectrometry》2010,21(4):670-680
We compare product-ion mass spectra produced by electron detachment dissociation (EDD) and electron photodetachment dissociation
(EPD) of multi-deprotonated peptides on a Fourier transform and a linear ion trap mass spectrometer, respectively. Both methods,
EDD and EPD, involve the electron emission-induced formation of a radical oxidized species from a multi-deprotonated precursor
peptide. Product-ion mass spectra display mainly fragment ions resulting from backbone cleavages of Cα-C bond ruptures yielding a and x ions. Fragment ions originating from N-Cα backbone bond cleavages are also observed, in particular by EPD. Although EDD and EPD methods involve the generation of a
charge-reduced radical anion intermediate by electron emission, the product ion abundance distributions are drastically different.
Both processes seem to be triggered by the location and the recombination of radicals (both neutral and cation radicals).
Therefore, EPD product ions are predominantly formed near tryptophan and histidine residues, whereas in EDD the negative charge
solvation sites on the backbone seem to be the most favorable for the nearby bond dissociation. 相似文献
10.
Pascale Lemoine Vincente Viossat Elie Dayan Dung Nguyen-Huy Bernard Viossat 《Journal of chemical crystallography》2010,40(10):852-858