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31.
A hydrophilic interaction liquid chromatography (HILIC) method was developed to measure the composition of humic substances from river, reservoir, and treated wastewater based on their physicochemical properties. The current method fractionates the humic substances into four well-defined groups based on parallel analyses with a neutral and a cationic HILIC column, using mobile phases of varied compositions and pH. The results indicate that: (i) the proportion of carboxylic acids in the humic substances from terrestrial origins is less than half of that from treated wastewater (Jeddah, KSA), (ii) a higher content of basic compounds was observed in the humic substances from treated wastewater and Ribou Reservoir (Cholet, France) than in the sample from Loire River (France), (iii) a higher percentage of hydrophobic macromolecules were found in the humic substances from Loire River than in the other samples, and (iv) humic substances of treated wastewater contained less ionic neutral compounds (i.e., pKa 5–9) than the waters from terrestrial origins. The physicochemical property disparity amongst the compounds in each humic substances sample was also evaluated. The humic substances from the lightly humic Loire river displayed the highest disparity, whereas the highly humic Suwannee river (Georgia, USA) showed the most homogeneous humic substances. 相似文献
32.
33.
High-precision isotope analysis is recognized as an essential research tool in many fields of study. Until recently, continuous flow isotope ratio mass spectrometry (CF-IRMS) was available via an elemental analyzer or a gas chromatography inlet system for compound-specific analysis of light stable isotopes. In 2004, however, an interface that coupled liquid chromatography with IRMS (LC/IRMS) became commercially available for the first time. This brought the capability for new areas of application, in particular enabling compound-specific δ(13)C analysis of non-volatile, aqueous soluble, compounds from complex mixtures. The interface design brought with it several analytical constraints, however, in particular a lack of compatibility with certain types of chromatography as well as limited flow rates and mobile phase compositions. Routine LC/IRMS methods have, however, been established for measuring the δ(13)C isotopic ratios of underivatized individual compounds for application in archeology, nutrition and physiology, geochemistry, hydrology, soil science and food authenticity. Seven years after its introduction, we review the technical advances and constraints, methodological developments and new applications of liquid chromatography coupled to isotope ratio mass spectrometry. 相似文献
34.
Rose-Munch F Marti A Cetiner D Tranchier JP Rose E 《Dalton transactions (Cambridge, England : 2003)》2011,40(7):1567-1575
First Suzuki-Miyaura coupling reactions applied to (η(5)-chloro-cyclohexadienyl)Mn(CO)3 complexes are described and lead to the syntheses of (η(5)-aryl-cyclohexadienyl)Mn(CO)3 and of cationic (η(6)-arene)Mn(CO)3 complexes after rearomatization. The structures of two of the new complexes have been investigated by X-ray diffraction study. 相似文献
35.
In this paper, we propose a new general method to compute rigorously global smooth branches of equilibria of higher-dimensional
partial differential equations. The theoretical framework is based on a combination of the theory introduced in Global smooth solution curves using rigorous branch following (van den Berg et al., Math. Comput. 79(271):1565–1584, 2010) and in Analytic estimates and rigorous continuation for equilibria of higher-dimensional PDEs (Gameiro and Lessard, J. Diff. Equ. 249(9):2237–2268, 2010). Using this method, one can obtain proofs of existence of global smooth solution curves of equilibria for large (continuous)
parameter ranges and about local uniqueness of the solutions on the curve. As an application, we compute several smooth branches
of equilibria for the three-dimensional Cahn–Hilliard equation. 相似文献
36.
37.
Hardelauf H Sisnaiske J Taghipour-Anvari AA Jacob P Drabiniok E Marggraf U Frimat JP Hengstler JG Neyer A van Thriel C West J 《Lab on a chip》2011,11(16):2763-2771
Spatially defined neuronal networks have great potential to be used in a wide spectrum of neurobiology assays. We present an original technique for the precise and reproducible formation of neuronal networks. A PDMS membrane comprising through-holes aligned with interconnecting microchannels was used during oxygen plasma etching to dry mask a protein rejecting poly(ethylene glycol) (PEG) adlayer. Patterns were faithfully replicated to produce an oxidized interconnected array pattern which supported protein adsorption. Differentiated human SH-SY5Y neuron-like cells adhered to the array nodes with the micron-scale interconnecting tracks guiding neurite outgrowth to produce neuronal connections and establish a network. A 2.0 μm track width was optimal for high-level network formation and node compliance. These spatially standardized neuronal networks were used to analyse the dynamics of acrylamide-induced neurite degeneration and the protective effects of co-treatment with calpeptin or brain derived neurotrophic factor (BDNF). 相似文献
38.
The structure and absolute configuration of natural 8-epi-9-deoxygoniopypyrone have been confirmed by an efficient and highly diastereoselective synthesis in 15 steps from (S)-mandelic acid with an overall yield of 43%. 相似文献
39.
Nathalie Deruelle Jean-Philippe Uzan 《International Journal of Theoretical Physics》1997,36(11):2461-2468
We briefly recall the problem of defining conserved quantities such as energy in general relativity, and the solution given
by introducing a symmetric background. We apply the general formalism to perturbed Robertson-Walker spacetimes with de Sitter
geometry as background. We relate the obtained conserved quantities to Traschen's integral constraints and mention a few applications
in cosmology. 相似文献
40.
Jean-Philippe Rocher Mohammed Ahmar Joelle Paris 《Journal of heterocyclic chemistry》1988,25(2):599-601
Condensation of dimethyl 3-methylglutaconate with ketones provides a one pot route for the preparation of 5-methoxycarbonyl-4-methyldihydropyran-2-ones. The experimental conditions to give selectively pyran-2-ones isomers are discussed. The structure of the different products was established on the basis of 1H and 13C nmr spectral data. 相似文献