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281.
M. H. T. Taddei J. F. Macacini R. Vicente J. T. Marumo S. K. Sakata L. A. A. Terremoto 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(3):2267-2272
The radionuclide 55Fe was determined in samples of radioactive wastes from the water cleanup system of the IEA-R1 nuclear research reactor. In order to validate the results, the 55Fe activity concentration was measured in eight waste samples and in six simulated samples containing the most important interfering radionuclides. A simple method was employed to separate and purify 55Fe from other radionuclides present in these samples, combining co-precipitation with ammonium hydroxide and purification with anionic ion-exchange resin, which enables 55Fe to be quantified either by liquid scintillation counting (LSC) or by X-ray spectrometry using a low-energy germanium spectrometer (LEGe). Both measurement methods were used so that the separation and purification process could be confirmed by comparison of spectra with and without the utilization of anionic ion-exchange resin. Activity and interferences were compared in the results obtained from LSC and LEGe measurement methods. 相似文献
282.
Silvia Tozzi Enrico Modena Stefano Falcioni Alessandra Sudanese Saverio Affatato Paola Taddei 《Journal of Raman spectroscopy : JRS》2014,45(9):781-787
Ultra‐high molecular weight polyethylene knee prostheses of two different sizes (i.e. characterised by different contact areas) were run on a knee wear simulator in two tests differing for the applied load. Gravimetric and micro‐Raman spectroscopic analyses were performed to investigate at macroscopic and molecular levels the effects of contact area and applied load on the morphology of the knee components. The larger prostheses showed a higher mass loss in both tests, while Raman spectroscopy showed a more significant polymer degradation in the smaller prostheses, suggesting that a lower contact area is responsible for a higher wear at the molecular wear, but for a lower gravimetric wear. Raman measurements showed that in the second test (using a higher applied load), the wear mechanism changed with respect to the first test: the less severe conditions used in the latter resulted in an increase in the orthorhombic content, while the more severe conditions used in the former determined an increase and rearrangement of the amorphous phase. The results here reported allow to gain more insights into the effects of contact area, applied load and contact stress on wear. Preliminary micro‐Raman analyses on in vivo worn knee prostheses confirmed the results obtained in vitro: the retrievals of smaller size were found more degraded at molecular level than those of larger size. These findings showed that the conditions used in the in vitro tests well simulate the knee kinematics of the knee joint and thus the in vivo wear. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
283.
Analytical quality by design in the development of a cyclodextrin‐modified capillary electrophoresis method for the assay of metformin and its related substances
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Serena Orlandini Benedetta Pasquini Roberto Gotti Alessandro Giuffrida Ferdinando Paternostro Sandra Furlanetto 《Electrophoresis》2014,35(17):2538-2545
Quality by Design (QbD) is a new paradigm of quality to be applied to pharmaceutical products and processes, recently encouraged by International Conference on Harmonisation guidelines. In this paper QbD approach was applied to the development of a CE method for the simultaneous assay of metformin hydrochloride (MET) and its main impurities. QbD strategy was focused on electrophoretic process understanding, and the analytical method was thoroughly evaluated by applying risk assessment and chemometric tools. Method scouting allowed CD‐CZE based on the addition of carboxymethyl‐β‐CD to Britton‐Robinson acidic buffer to be chosen as operative mode. Seven critical process parameters (CPPs) were selected, related to capillary, injection, BGE and instrumental settings. The effect of the different levels of the CPPs on critical quality attributes (CQAs), e.g. critical resolution values and analysis time, was evaluated in a screening study. Response surface methodology led to draw contour plots and sweet spot plots. The definition of design space was accomplished by applying Monte‐Carlo simulations, thus identifying by risk of failure maps a multivariate zone where the CQAs fulfilled the requirements with a selected probability. Finally, a control strategy was designed and the method was applied to a real sample of MET tablets. 相似文献
284.
Eliana Aparecida Nonato Knupp Camilla Gonçalves Bof Silva Kerley Alberto Pereira de Oliveira Flávia Regina de Amorim Maria Célia Siqueira Maria Helena Tirollo Taddei Milton Batista Franco Helena Eugênia Leonhardt Palmieri Vanusa Maria Feliciano Jacomino 《Journal of Radioanalytical and Nuclear Chemistry》2014,299(1):321-327
Phosphogypsum (PG) is a by-product of the phosphate fertilizer industry, which is produced by precipitation during the wet process of phosphate rocks. While commercial uses, in agriculture and in manufacturing gypsum board and Portland cement, consume less than a few percent of this by-product, the vast majority is disposed of on land in gypsum. In Brazil, three main industries are responsible for the production and storage of about 5.5 × 106 tons per year. PG may contain trace metals, non-metals, fluorides and natural radionuclides. Since, in Brazil, PG has been used for many years as soil amendment, it is important to know its availability, mainly in aquatic environments used for human consumption. In this case, more restrictive limits must be adopted. This work aimed to evaluate the mobility of metals in sand and clayey soils and, consequently, the contamination of drainage water through greenhouse-scale leaching and transport of toxic elements and radionuclides from soils fertilized with PG to crops. In general, it was observed that elemental concentrations were below the actual detection limit of the equipment for all conditions of interest, indicating a low mobility of the analyzed elements in the soil. 相似文献
285.
3D‐printed photo‐spectroelectrochemical devices for in situ and in operando X‐ray absorption spectroscopy investigation
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286.
Lanciaquinone, isolated from Maesa lanceolata, was originally assigned as a bisbenzoquinone with a C14-chain linking the two quinone rings. A synthesis of the reported structure, in which the key step is a double Claisen rearrangement, suggests that the structure of the natural product needs to be revised. 相似文献
287.
Gentili PL Presciutti F Evangelisti F Costantino F 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(14):4296-4307
A new family of layered metal(III)-phosphono-carboxylate nanostructures (M=Y, Eu, Tb, Er, and Yb) was hydrothermally synthesized and their structures and morphologies were characterized by X-ray powder diffraction and TEM. 4-[Bis(phosphonomethyl)amino]caproic acid and 4- [bis(phosphonomethyl)amino]undecanoic acid, with general formula (H(2)O(3)PCH(2))(2)NR (R=C(5)H(10)COOH(P2CAPR) and C(10)H(22)COOH(P2UND), respectively) were used as building blocks for the preparation of novel layered hybrid materials in which the inorganic layers were composed of MO(7) or MO(8) polyhedra and PO(3)C tetrahedra. The interlayer region was occupied by carboxyalkyl chains. These layered compounds were easily dispersed as stable solutions in alkylamine/water upon ultrasonication. These dispersions were constituted of rectangular elongated nanoparticles (NPs), which showed a distribution of sizes ranging from 20-500 nm. These new materials had interesting photophysical properties because they were multiluminescent compounds. These properties gave rise to several emission bands, which were spread over the broad spectroscopic region, from the near-UV up to the near-IR regions. Each emission band had a specific lifetime, which ranged from the sub-ps to the ms scale. 相似文献
288.
Cardullo F Donati D Fusillo V Merlo G Paio A Salaris M Solinas A Taddei M 《Journal of combinatorial chemistry》2006,8(6):834-840
One of the still unresolved problems in parallel synthesis is the availability of a general and rapid method for the transformation of a primary amine into the corresponding secondary amine without the issue of polyalkylation. Following the Fukuyama method, which is based on the alkylation of o-nitrobenzenesulfonamides, followed by removal of the sulfonyl group, we have developed a simple protocol which can be easily applied to parallel synthesis making use of supported reagents and scavengers. To verify the robustness of the method, a small representative array of secondary amines have been prepared. Moreover, taking advantage of the possibility to use different supported reagents in the same pot, we also prepared, starting from primary amines, a series of differently substituted tertiary amines. 相似文献
289.
Girotti R Marrocchi A Minuti L Piermatti O Pizzo F Vaccaro L 《The Journal of organic chemistry》2006,71(1):70-74
[reaction: see text] Diels-Alder reactions of 3-substituted coumarins 1a-g with methyl-1,3-butadienes 2a-c carried out in water alone and in CH2Cl2 under 9 kbar pressure are reported. In aqueous medium satisfactory results were obtained by operating at 150 degrees C, whereas under high pressure the cycloadditions were complete at 60-70 degrees C with excellent yields (85-95%). The reactions with isoprene (2b) always resulted in the exclusive formation of para cycloadducts, whereas with (E)-piperylene (2c) only ortho products were detected. The cycloaddition of 3-phenylsulfonylcoumarin (1a) with (E)-piperylene (2c) allowed the endo adduct to be obtained exclusively, whereas 3-carboxycoumarin (1b) reacted with 2c to give a mixture of the corresponding endo/exo adducts in a 58:42 ratio in water and in a 45:55 ratio under high-pressure condition. 相似文献
290.
Curcumin, a well-known Indian spice, holds a variety of properties in many different fields from medicinal chemistry to dye industry. The peculiar electronic structure makes curcumin a valuable metal chelator. The principal aim of this work is a computational study of the structural and electronic properties of the ground and the first singlet excited states of the curcuminoidic core. Concerning the ground state, tautomeric equilibrium, vibrational and thermochemical analysis and electronic absorption spectra (with ab initio and semi-empirical methodologies) have been studied. A full geometry optimization of the first singlet excited states was obtained, with different computational methodologies. Solvent effects are also implicitly considered. An accurate comparison of the results is presented. Interesting aspects emerge, which suggest successive investigation about the nature of the excited states. The obtained results may be of large applicative interest. If curcuminoids are considered as potential ligands for complexes formation with metallic ions of pharmaceutical, medical–physical and technological interest, exciting the system with photons of appropriate frequencies, a photomodulated release of the metallic ion in the environment might be guessed, because of an important photoinduced geometrical modification. 相似文献