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11.
The Lyapunov vectors corresponding to the steps of Lyapunov spectra for many-particle systems show time-oscillating behavior in two types of Lyapunov modes, one associated with time-translational invariance and the other with spatial translational invariance. Our result is that, for each coordinate direction, the longest period of the Lyapunov modes is twice as long as the period of the momentum autocorrelation function. A simple explanation for this relation is proposed and we argue that this result is generally true for many-particle systems. This gives the first quantitative connection between the Lyapunov modes and an experimentally accessible quantity. 相似文献
12.
Tooru Kitagawa Kohji Tashiro Kazuyuki Yabuki 《Journal of Polymer Science.Polymer Physics》2002,40(13):1281-1287
Fourier transform Raman spectra were measured for poly‐p‐phenylenebenzobisoxazole (PBO) fiber subjected to a tensile stress, and the Raman shift factor (the frequency shift caused by 1 GPa tensile stress) depended strongly on the sample‐preparation condition. To clarify the reasons of this dependency, a mechanical series parallel model was adopted that could successfully and quantitatively explain the observed Raman shift factors and gave a concreate heterogeneous stress distribution in the PBO fibers. As a result, a mechanical series model was reasonable for PBO fiber. Broadening of Raman bands, which was observed when the PBO fiber was tensioned, could also be interpreted on the basis of an idea of heterogeneous stress distribution. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1281–1287, 2002 相似文献
13.
Summary Boric and germanic acids were detected by a conductivity detector after ion-exclusion Chromatographic separation on a cation-exchange resin. Neither acid could be directly measured by a conductivity detector because they were very weak. However, use of eluents of polyol compounds permitted their determination by a conductivity detector. With 0.1 M of fructose as eluent, it was possible to detect 0.5 ppb of boric acid (as B) and 1.5 ppb of germanic acid (as Ge).
HPLC-Bestimmung von Borsäure und Germaniumsäure mit konduktometrischer Detection
Zusammenfassung Beide Säuren wurden mit Hilfe eines Leitfähigkeitsdetektors nach Trennung durch Ionenausschluß-Chromatographie an einem Kationenaustauscher analysiert. Eine direkte Messung war wegen der Schwäche der Säuren nicht möglich; daher wurde eine Elution mit Polyolen durchgeführt. Mit 0,1 M Fructoselösung als Eluens konnten noch 0,5 ppb Borsäure (als B) und 1,5 ppb Germaniumsäure (als Ge) nachgewiesen werden.相似文献
14.
Otani M Taniguchi T Sakai A Seta J Kadoyama K Nakamura-Hirota T Matsuyama S Sano K Takano M 《Applied biochemistry and biotechnology》2011,164(6):804-818
We validated the novel PhosphoQUANTI SolidBlue Complex (PQSC) dye for the sensitive fluorescent detection of phosphorylated proteins in polyacrylamide- and two-dimensional gel electrophoresis (PAGE and 2DE, respectively). PQSC can detect as little as 15.6 ng of ß-casein, a pentaphosphorylated protein, and 61.3 ng of ovalbumin, a diphosphorylated protein. Fluorescence intensity correlates with the number of phosphorylated residues on the protein. To demonstrate the specificity of PQSC for phosphoproteins, enzymatically dephosphorylated lysates of Swiss 3T3 cells were separated in 2DE gels and stained by PQSC. The fluorescence signals in these gels were markedly reduced following dephosphorylation. When the phosphorylated proteins in Swiss 3T3 cell lysates were concentrated using a phosphoprotein enrichment column, the majority of phosphoproteins showed fluorescence signals in the pI 4–5 range. Finally, we performed phosphoproteome analysis to study differences in the protein phosphorylation profiles of proliferating and quiescent Swiss 3T3 cells. Over 135 discernible protein spots were detected, from which a selection of 15 spots were identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF-MS). The PQSC staining procedure for phosphoprotein detection is simple, reversible, and fully compatible with MALDI TOF-MS. 相似文献
15.
Arai M. Sakuma T. Atake T. Kawaji H. 《Journal of Thermal Analysis and Calorimetry》2002,69(3):905-908
The phase transition and the crystal structures of CuITe were investigated by differential thermal analysis and X-ray powder
diffraction measurements in the temperature range between 300 and 683 K. The new phase transition in CuITe was observed at
592 K. The enthalpy of transition is ΔH=0.125 kJ mol-1. The new phase above 592 K belongs to tetragonal system with the space group I41
/amd.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
16.
Preparation of Cu2ZnSnS4 thin films by hybrid sputtering 总被引:2,自引:0,他引:2
Tooru Tanaka Takeshi Nagatomo Mitsuhiro Nishio Akihiro Wakahara Hiroshi Ogawa 《Journal of Physics and Chemistry of Solids》2005,66(11):1978-1981
In order to fabricate Cu2ZnSnS4 thin films, hybrid sputtering system with two sputter sources and two effusion cells is used. The Cu2ZnSnS4 films are fabricated by the sequential deposition of metal elements and annealing in S flux, varying the substrate temperature. The Cu2ZnSnS4 films with stoichiometric composition are obtained at the substrate temperature up to 400 °C, whereas the film composition becomes quite Zn-pool at the substrate temperature above 450 °C. The Cu2ZnSnS4 film shows p-type conductivity, and the optical absorption coefficient and the band gap of the Cu2ZnSnS4 film prepared in this experiment are suitable for fabricating a thin film solar cell. 相似文献
17.
The addition of 1,10-phenanthroline improves both the extraction and the spectrophotometric sensitivity of the determination of cadmium with diphenylcarbazone. Slope analysis suggests the formation of a 1:2:2 extracted species. The molar absorptivity is 9.4 × 104 l cm-1 mol-1 at 536 nm and extraction is maximal at pH 8.2–9.8. Extraction is rapid and absorbances remain constant at room temperature for 48 h. Various divalent metal ions interfere. 相似文献
18.
Shimizu Y Ohte Y Yamamura Y Saito K Atake T 《The journal of physical chemistry. B》2006,110(28):13970-13975
Heat capacities of liquid, stable crystal, and liquid-quenched glass of a room-temperature ionic liquid (RTIL), 1-hexyl-3-methylimidazolium bis(trifluromethylsulfonyl)imide were measured between 5 and 310 K by adiabatic calorimetry. Heat capacity of the liquid at 298.15 K was determined for an IUPAC project as (631.6 +/- 0.5) J K(-1) mol(-1). Fusion was observed at T(fus) = 272.10 K for the stable crystalline phase, with enthalpy and entropy of fusion of 28.34 kJ mol(-1) and 104.2 J K(-1) mol(-1), respectively. The purity of the sample was estimated as 99.83 mol % by the fractional melting method. The liquid could be supercooled easily and the glass transition was observed around T(g) approximately 183 K, which was in agreement with the empirical relation, T(g) approximately ((2)/(3)) T(fus). The heat capacity of the liquid-quenched glass was larger than that of the crystal as a whole. In the lowest temperature region, however, the difference between the two showed a maximum around 6 K and a minimum around 15 K, at which the heat capacity of the glass was a little smaller than that of crystal. 相似文献
19.
A phosphorus-containing hybrid porphyrin was successfully prepared via the BF3-promoted dehydrative condensation between sigma4-phosphatripyrrane and 2,5-bis[hydroxy(phenyl)methyl]thiophene. The NMR and UV-vis absorption spectra, electrochemical measurements, and DFT calculations revealed that the sigma3-P,N2,S-hybrid porphyrin exhibits high aromaticity as an 18pi-electron system in terms of both geometric and magnetic criteria. [structure: see text] 相似文献
20.
Ooya T Inoue D Choi HS Kobayashi Y Loethen S Thompson DH Ko YH Kim K Yui N 《Organic letters》2006,8(15):3159-3162
[Structure: see text] A polypseudorotaxane consisting of cucurbit[7]uril (CB[7])/N,N'-(3-phenylenebis(methylene)dipropargylamine (PMPA), [2]pseudorotaxane, and 2,6-O-dimethyl beta-cyclodextrin (DM-beta-CD)/alpha,omega-bisazidopropylene glycol 400 [2]pseudorotaxane was synthesized using the "click" reaction. The polypseudorotaxane structure was maintained in aqueous solution over a wide range of pH values with the DM-beta-CD units contributing to increased solubilization of the polypseudorotaxane without dethreading. The pH-responsive movement of the CB[7] units in the polypseudorotaxane was also observed. 相似文献