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31.
Giovanni Pellegrino Angelo Carotti Orazio Nicolotti Leonardo Pisani Angela Stefanachi Marco Catto 《Tetrahedron letters》2010,51(13):1702-7034
A small molecular library of 40 pyrimidine, pyrazole, and isoxazole derivatives, bearing structural features for a promising binding of therapeutically interesting enzymes, was designed and prepared. An efficient and straightforward solid phase synthesis was envisaged and carried out on a Rink amide resin. The assistance of microwave heating in any step reduced the reaction time, increased the reaction yields, and allowed an easy work-up and purification of the targeted compounds. 相似文献
32.
Donato Ercole Conte Abdelmaula Aboulaich Josette Olivier-Fourcade Christian Jordy 《Journal of solid state chemistry》2010,183(1):65-6650
A comparative study of two Sn-based composite materials as negative electrode for Li-ion accumulators is presented. The former SnB0.6P0.4O2.9 obtained by in-situ dispersion of SnO in an oxide matrix is shown to be an amorphous tin composite oxide (ATCO). The latter Sn0.72[BPO4]0.28 obtained by ex-situ dispersion of Sn in a borophosphate matrix consists of Sn particles embedded in a crystalline BPO4 matrix. The electrochemical responses of ATCO and Sn0.72[BPO4]0.28 composite in galvanostatic mode show reversible capacities of about 450 and 530 mAh g−1, respectively, with different irreversible capacities (60% and 29%). Analysis of these composite materials by 119Sn Mössbauer spectroscopy in transmission (TMS) and emission (CEMS) modes confirms that ATCO is an amorphous SnII composite oxide and shows that in the case of Sn0.72[BPO4]0.28, the surface of the tin clusters is mainly formed by SnII in an amorphous interface whereas the bulk of the clusters is mainly formed by Sn0. The determination of the recoilless free fractions f (Lamb-Mössbauer factors) leads to the effective fraction of both Sn0 and SnII species in such composites. The influence of chemical composition and especially of the surface-to-bulk tin species ratio on the electrochemical behaviour has been analysed for several Snx[BPO4]1−x composite materials (0.17<x<0.91). The cell using the compound Sn0.72[BPO4]0.28 as active material exhibits interesting electrochemical performances (reversible capacity of 500 mAh g−1 at C/5 rate). 相似文献
33.
Tien-Yu Wang Guan-Liang Chen Chao-Chiang Hsu Sarah Vied Eric D. Conte Shing-Yi Suen 《Microchemical Journal》2010,96(2):290-295
In this study, octadecyltrimethylammonium surfactant was immobilized onto a cation exchange membrane for the application in solid-phase extraction of phenolic compounds. The results indicate that an HCl prewashing step and the use of hydroxide (or methoxide) counter ion could greatly improve the immobilized surfactant capacity. Through elemental and thermogravimetric analyses, the resulted immobilization percentage on the membrane (compared to membrane ion exchange capacity) was about 50, 100, and 150%, respectively, for the feed surfactant amount of 150, 2000, and 5000 μmol (volume = 20 mL). Phenol, 4-nitrophenol, 2,4-dimethylphenol, 2,4-dichlorophenol, 4-chloro-3-methylphenol, and bisphenol A were the tested compounds in a breakthrough volume experiment. The order of the obtained breakthrough volume values is similar to that of Kow values of the phenolic compounds. In the solid-phase extraction process from a feed mixture of 0.1 ppm for 4-nitrophenol, 2,4-dichlorophenol, and 4-chloro-3-methylphenol, high concentration factors and almost complete recoveries were achieved. Moreover, by increasing the membrane volume, a larger sample volume could be processed without any deterioration in performance. 相似文献
34.
Giorgia Purcaro Peter Quinto Tranchida Paola Dugo Erminia La Camera Giuseppe Bisignano Lanfranco Conte Luigi Mondello 《Journal of separation science》2010,33(15):2334-2340
The bacteria fatty acid profile has been extensively studied for taxonomic classification purposes, since bacteria, in general, contain particular and rare fatty acids, compared with animal and plant tissues. As for any real‐world sample type, the development of rapid and reliable methods for (i) sample identification (in this case, bacterium type), and (ii) constituent identification (in this instance, the fatty acid profile) is desirable. In this research, a half‐an‐hour procedure, to analyze bacteria, was developed: a 2‐min one‐step sample preparation step was followed by a relatively fast comprehensive 2D GC‐MS separation (25 min). Furthermore, dedicated MS libraries were constructed for the identification of bacteria and fatty acids. Finally, data processing, only qualitative at this stage, was carried out with the support of a novel comprehensive 2D GC software. 相似文献
35.
Flavio Ceretta Alessandro Zaggia Lino Conte Bruno Ameduri 《Journal of polymer science. Part A, Polymer chemistry》2013,51(15):3202-3212
4′‐Nonafluorobutylstyrene (3) was synthesized and polymerized by conventional and controlled radical polymerization (iodine transfer polymerization (ITP)). Such an aromatic fluoromonomer was prepared from Ullmann coupling between 1‐iodoperfluorobutane and 4‐bromoacetophenone followed by a reduction and a dehydration in 50% overall yield. Two radical polymerizations of (3) were initiated by AIBN either under conventional or controlled conditions, with 1‐iodoperfluorohexane in 84% monomer conversion and in 50% yield. ITP of (3) featured a fast monomer conversion and a linear evolution of the ln([M]0/[M]) versus time. The kinetics of radical homopolymerization of (3) enabled one to assess its square of the propagation rate to the termination rate (kp2/kt) in ITP conditions (36.2·10?2 l·mol?2·sec?2 at 80 °C) from the Tobolsky's kinetic law. Polydispersity index (?) of the fluoropolymer achieved by conventional polymerization was 1.30 while it worthed 1.15 when synthesized by ITP. Thermal stabilities of these oligomers were satisfactory (10% weight loss under air occurred from 305 °C) whereas the melting point was 47 °C. Contact angles and surface energies assessed from spin‐coated poly(3) films obtained by conventional (hysteresis = 18°, surface energy 18 mN.m?1) and ITP (hysteresis = 47°, surface energy 15 mN.m?1) evidenced ? values' influence onto surface properties of the synthesized polymers. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3202–3212 相似文献
36.
Rosa Ana Conte M. T. C. de Loos-Vollebregt 《Analytical and bioanalytical chemistry》2000,367(8):722-726
Cobalt in sludge of domestic and industrial origin, with high iron contents (> 17 g/kg), was determined by slurry sampling graphite furnace atomic absorption spectrometry (GF-AAS). Slurries prepared by ultrasonic stirring were adequately diluted to cover the variation in cobalt content in the sludge samples. The diluent was 5% HNO3. Standard atomisation conditions for cobalt determination were used and no matrix modifier was applied. Slurry sampling GF-AAS results in the sludge were verified by analysing totally digested samples by inductively coupled plasma atomic emission spectrometry (ICP-AES) and by GF-AAS. The procedure was validated by analysing the certified reference material BCR 146 R, a sewage sludge of industrial origin. Recoveries for cobalt in the spiked slurried sludge samples ranged from 92 to 96%, with a relative standard deviation of 10%. Recoveries in the certified sludge using slurry sampling GF-AAS technique were about 103% for a cobalt content of 7.39 mg/kg. 相似文献
37.
Rosa Ana Conte Eric H. van Veen M. T. C. de Loos-Vollebregt 《Analytical and bioanalytical chemistry》1999,364(7):666-672
Prehydrolysate samples from the acidic prehydrolysis of Eucalyptus wood residues were submitted to survey analysis by inductively coupled plasma (ICP) optical emission spectrometry (OES) based on the multicomponent and multiline techniques. The survey analysis software is designed to determine 64 elements. The semiquantitative data obtained for the unknown prehydrolysate samples provided fast and valuable information for the determination of important inorganic constituents (Al, B, Ba, Ca, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, S, Si, Sr, Zn, Co, Pb, Sn) for further utilisation of the prehydrolysate in the production of fertilisers, animal feed and furfural. To validate the survey analysis approach, the prehydrolysate samples were quantitatively analysed by the standard additions method. For the prehydrolysate samples the relative difference between the results obtained by both techniques was generally ± 25% for the majority of the elements, a typical value for the survey approach. Analyte recoveries in the spiked prehydrolysate samples analysed by the survey approach ranged from 95 to 125%. Independent replicates of prehydrolysate samples were measured over a 15-day period showing relative standard deviations of ≤ 4% for all elements, except for Zn (10%) and S (16%). 相似文献
38.
39.
In this paper we give a systematized treatment to some coincidence situations for multiple summing multilinear mappings which extend, generalize and simplify the methods and results obtained thus far. The application of our general results to the pertinent particular cases gives several new coincidences as well as easier proofs of some known results (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
40.
Dr. Alessandra Alberti Dr. Ioannis Deretzis Dr. Giovanna Pellegrino Dr. Corrado Bongiorno Dr. Emanuele Smecca Dr. Giovanni Mannino Dr. Filippo Giannazzo Prof. Guglielmo Guido Condorelli Dr. Nobuya Sakai Prof. Tsutomu Miyasaka Dr. Corrado Spinella Dr. Antonino La Magna 《Chemphyschem》2015,16(14):3064-3071
We investigate the degradation path of MAPbI3 (MA=methylammonium) films over flat TiO2 substrates at room temperature by means of X‐ray diffraction, spectroscopic ellipsometry, X‐ray photoelectron spectroscopy, and high‐resolution transmission electron microscopy. The degradation dynamics is found to be similar in air and under vacuum conditions, which leads to the conclusion that the occurrence of intrinsic thermodynamic mechanisms is not necessarily linked to humidity. The process has an early stage, which drives the starting tetragonal lattice in the direction of a cubic atomic arrangement. This early stage is followed by a phase change towards PbI2. We describe how this degradation product is structurally coupled with the original MAPbI3 lattice through the orientation of its constituent PbI6 octahedra. Our results suggest a slight octahedral rearrangement after volatilization of HI+CH3NH2 or MAI, with a relatively low energy cost. Our experiments also clarify why reducing the interfaces and internal defects in the perovskite lattice enhances the stability of the material. 相似文献