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排序方式: 共有115条查询结果,搜索用时 125 毫秒
21.
Piercarlo Mustarelli Corrado Tomasi Marco Villa Gian Battista Appetecchi Fausto Croce 《Ionics》1995,1(2):147-152
Two composite gel electrolytes prepared from mixtures of poly(acrylonitrile) (PAN), propylene carbonate (PC), ethylene carbonate
(EC) and LiClO4 have been studied with differential scanning calorimetry (DSC) and7Li-6Li NMR. The data allow estimation of ionic conductivities, local (short range) diffusivities, and lattice dynamics. Furthermore,
they point to an unexpected behavior of the Li-rich sample that hints to a complex LiClO4-PAN phase diagram.
Paper presented at the 1st Euroconference on Solid State Ionics, Zakynthos, Greece, September 11–18,1994 相似文献
22.
Giuseppe Cremonesi Piero Dalla Croce Alessandra Forni Maddalena Gallanti Raffaella Gandolfi Concetta La Rosa 《Tetrahedron: Asymmetry》2009,20(16):1940-1947
Enantiomerically pure (5R)-(?)-5-phenyl-4,5-dihydroisoxazole-3-carboxylic acid ethyl ester was obtained via enzymatic resolution of the corresponding racemic mixture using a lipase from hog pancreas (PPL). The following reduction of the ester group to the corresponding alcohol and the oxidation of the latter led to (5R)-(?)-5-phenyl-4,5-dihydroisoxazole-3-carbaldehyde, and the reaction between this and Schöllkopf’s reagent, (2R)-(+)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine, gave mixtures of adducts with a good syn/anti ratio. The steric configurations of the major diastereoisomer were assigned on the basis of spectroscopic data and X-ray analysis. The subsequent controlled hydrolysis of the pyrazine ring led to β-(5-phenyl-4,5-dihydroisoxazol-3-yl)-serine methyl esters and the corresponding dipeptides with (R)-valine. Finally, reductive cleavage of the 4,5-dihydroisoxazole ring under hydrolytic conditions made it possible to obtain the corresponding polyfunctionalised dipeptides. 相似文献
23.
In the range of low enough spatial frequencies the roughness power spectrum of mechanically polished glass surfaces appears to follow an inverse law of the scattered wave vector. This decrease is likely to agree with a crossed line configuration resulting from the polishing process. Comparison is made with an imperfect polish and a fine polish. 相似文献
24.
Caterina Rinaudo Mario Allegrina Elisa Fornero Maya Musa Alessandro Croce Donata Bellis 《Journal of Raman spectroscopy : JRS》2010,41(1):27-32
Histological sections of a patient affected by an important respiratory disease were analysed firstly by optical microscope(OM)—crossed polarisers—to identify the presence of incorporated inorganic particles, with particular attention to the fibrous ones. Then, the particles/fibres that were found were studied both with micro‐Raman spectroscopy and variable‐pressure scanning electron microscopy with energy‐dispersive spectroscopy (VP‐SEM/EDS). The two techniques allowed the in situ characterisation of the inorganic phases without disintegration of the organic matter. Micro‐Raman spectroscopy was able to identify the vibrating chemical groups of the mineral phase associated with the inorganic grain while the crystalline structure was preserved by the biological system. The VP‐SEM/EDS characterisation, defining the elemental chemical composition of the analysed particle/fibre, allowed confirmation of the mineral phase deducible from spectroscopic data or its identification with certainty when the spectroscopic data were not exhaustive. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
25.
V. Rossi Albertini G. B. Appetecchi R. Caminiti F. Croce F. Cilloco C. Sadun 《Journal of Macromolecular Science: Physics》2013,52(5):629-641
The crystallization kinetics of poly(ethylene oxide) doped with various alkaline perchlorate salts were measured at room temperature by means of the new energy dispersive x-ray diffraction method for the phase transition. The experimental points of the transformation coordinate were fitted using the phenomenological Liquori-Tripiciano law, the parameters of which were evaluated for each case. The influence of the concentration and of the cation dimensions on the crystallization rate is discussed. Further details about the application of this nonconventional diffractometric technique to polymers are also reported, as is an intuitive model for describing the method. 相似文献
26.
Maroni Fabio Bruni Pantaleone Suzuki Naoki Aihara Yuichi Croce Fausto 《Journal of Solid State Electrochemistry》2019,23(6):1697-1703
Journal of Solid State Electrochemistry - All-solid-state batteries represent the next generation of electrochemical energy storage systems. A tin-carbon nanocomposite material is prepared by the... 相似文献
27.
Lucia Giorgetti Gianluca Giorgi Edoardo Cherubini Pier Giovanni Gervasi Clara Maria Della Croce Vincenzo Longo 《Natural product research》2018,32(14):1617-1626
We report the spectrophotometric determination of total polyphenols, flavonoids, glucosinolates and antioxidant activity in seeds, seedlings and leaves of Tuscan black kale. The highest content of phytochemicals was observed in 10 days sprouts and antioxidant activity was maximum in 2, 4 days seedlings. Identification and characterisation of phytochemicals were performed by mass spectrometry (MS), high resolution and tandem MS with electrospray ionisation mode. Low-molecular-weight metabolites were evidenced in seeds while metabolites at high m/z range were detected in cotyledons and leaves. MS spectra evidenced different phenolic compounds (flavonoid caffeoyl glucose, hydroxycinnamic acid sinapine) and glucosinolates (glucoerucin, glucobrassicin and glucoraphanin) in function of developmental stage; galactolipids ω3 and ω6 were observed in leaves. Identification of stages with the highest phytochemicals content encourages the consumption of black kale sprouts and young leaves. Our research can support food and pharmaceutical industries for production of health promoting products from black kale. 相似文献
28.
Milanesio M Croce G Viterbo D Pastore HO Mascarenhas AJ Munsignatti EC Meda L 《The journal of physical chemistry. A》2008,112(36):8403-8410
29.
G. B. Appetecchi F. Croce F. Ronci B. Scrosati F. Alessandrini M. Carewska P. P. Prosini 《Ionics》1999,5(1-2):59-63
In the development of rechargeable lithium polymer batteries it is of paramount importance to control the passivation phenomena
occurring at the lithium electrode interface. It is well estabilished that the type and the growth of the lithium passivation
layer is unpredictably influenced by the presence of liquid components and/or impurities in the electrolyte. Therefore, one
approach to improve the stability of the lithium interface is the use of liquid-free, highly pure electrolytes.
The electrochemical properties of a composite polymer electrolyte obtained by hot pressing a mixture of polyethylene oxide
(PEO), a lithium salt (lithium tetrafluoroborate, LiBF4) and a powdered ceramic additive (γ-LiAlO2), will be presented and discussed.
The electrochemical characterization included the determination of the ionic conductivity, the anodic break-down voltage and,
most importantly, the stability of the lithium metal electrode interface and the lithium stripping-plating process efficiency.
The main feature of this dry, true solid-state electrolyte is a very good compatibility with the lithium metal electrode,
demonstrated by a very high lithium cycling efficiency, which approaches a value of 99%.
Paper presented at the 5th Euroconference on Solid State Ionics, Benalmádena, Spain, Sept. 13–20, 1998. 相似文献
30.
Aubriet F Muller JF Poleunis C Bertrand P Di Croce PG Grange P 《Journal of the American Society for Mass Spectrometry》2006,17(3):406-414
Since the discovery of the Phillips catalysts, there still is much uncertainty concerning their activation, their molecular structure, the nature of the active chromium sites, and the polymerization mechanisms. Surface techniques are not easy to be used for such study according to the nonconductive behavior of the support. Therefore, model Phillips catalyst is elaborated by spin coating a trivalent chromium precursor on a silicon wafer. The surface characterization of this model catalyst is conducted by laser ablation mass spectrometry (LA-MS), laser desorption/ionization mass spectrometry (LDI-MS), and static secondary ion mass spectrometry (s-SIMS), at different steps of its preparation. To validate our approach, a comparison is also made between the model and the real Philips catalyst. Moreover, the model catalyst efficiency for polyethylene synthesis is evaluated and allows us to discuss the validity of the mechanisms previously proposed to explain the catalytic process. The characterization of Phillips model catalyst by mass spectrometry allows us to better understand the activation processes of such catalyst. Depending on the activation temperature, chromium oxide species are formed and anchored at the support surface. They consist mainly in mono-chromium sites at high temperature. The chromium valence is hexavalent. This model catalyst is active for the polymerization of ethylene. A pseudo-oligomer molecular weight distribution is observed by LA-MS, whereas s-SIMS allows us to elucidate the anchorage of the polymer at activate chromium surface sites. 相似文献