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1.
Motivated by some functional models arising in fuzzy logic, when classical boolean relations between sets are generalized,
we study the functional equation S(S(x, y), T(x, y)) = S(x, y), where S is a continuous t-conorm and T is a continuous t-norm. Some interesting methods for solving this type of equations are introduced. 相似文献
2.
Stable cyclotriphosphazenes 4 and 5, incorporating one and two carbon radical centers, respectively, have been easily prepared and characterized. EPR spectroscopic studies in fluid solution at room temperature were carried out for both compounds and also for diradical 5 in frozen solvent matrixes. Spectral results are consistent with a triplet or degenerate singlet triplet ground state for 5. Reductive cyclic voltammetry shows a redox couple, being monoelectronic for 4 and bielectronic for 5. 相似文献
3.
Photocyclization of 2-chloroacetyl-1,2,3,4,5,6-hexahydro-1, 5-methanoazocino[4,3-b]indole () takes place at the indole 4-position to give a 1 ,2 ,3 ,4 , 5 ,6-hexahydro-2 ,11-ethano-1 ,5-methanoazocino [4 , 3-6] indole system. Consequently, the method appears to be unsuitable for constructing the pyrrolidine ring of pentacyclic Strychnos indole alkaloids. 相似文献
4.
The self-assembly mechanisms of polyoxometalates (POMs) are still a matter of discussion owing to the difficult task of identifying all the chemical species and reactions involved. We present a new computational methodology that identifies the reaction mechanism for the formation of metal-oxide clusters and provides a speciation model from first-principles and in an automated manner. As a first example, we apply our method to the formation of octamolybdate. In our model, we include variables such as pH, temperature and ionic force because they have a determining effect on driving the reaction to a specific product. Making use of graphs, we set up and solved 2.8 × 105 multi-species chemical equilibrium (MSCE) non-linear equations and found which set of reactions fitted best with the experimental data available. The agreement between computed and experimental speciation diagrams is excellent. Furthermore, we discovered a strong linear dependence between DFT and empirical formation constants, which opens the door for a systematic rescaling.The self-assembly mechanisms of polyoxometalates (POMs) are still a matter of discussion owing to the difficult task of identifying all the chemical species and reactions involved. The POMSimulator deals with that complexity in an automated manner. 相似文献
5.
Zorana Grabari Boidar S. Grabari Miquel Esteban Enric Casassas 《Journal of Electroanalytical Chemistry》1997,420(1-2)
Ratio differential pulse polarograms obtained by dividing the multianalyte and single analyte signals are proposed as a tool for resolution of global signals and quantification of the analytes from a qualitatively known mixture by differential pulse polarography (DPP) and related electroanalytical techniques. The influences of shape and position of the resolving function (DP polarograms of individual analyte) on the efficiency of resolution are discussed on simulated and experimental results. The method is applied for the determination of p-nitroaniline (NA) and p-nitrotoluene (NT) from their mixture in N,N′-dimethylformamide solutions with 0.1 M tetrabutylammonium iodide as supporting electrolyte, using an external calibration diagram and internal standard addition methods. NA and NT give one-electron DP polarographic peaks with 93 mV of peak separation and, therefore, show significant overlapping which depends on the concentration ratio of NA and NT in the mixture. The method is especially suitable for quantification of one analyte in the presence of a large excess of another analyte, because by division the component in excess is removed and the pseudo-ratio DPP of the minor component is clearly revealed in a way which is not possible by deconvolution using polynomial division or deconvolution by Fourier transforms. 相似文献
6.
Baudron SA Batail P Rovira C Canadell E Clérac R 《Chemical communications (Cambridge, England)》2003,(15):1820-1821
Neutral pi-conjugated molecules and their radical cations co-exist in [(EDT-TTF-CONHMe+*)4(EDT-TTF-CONHMe0)2] [Re6Se8(CN)6]4- (CH3CN)2(CH2Cl2)2 whose crystal structure reveals that, upon one-electron oxidation, an activation of the N-H and C-H hydrogen bond donor ability is coupled to a deactivation of the hydrogen bond acceptor character of the carbonyl oxygen atom: this is expressed in the supramolecular hydrogen bond pattern and, ultimately, into charge localisation and partition in the solid state. 相似文献
7.
Comas E Gimeno RA Ferré J Marcé RM Borrull F Rius FX 《Journal of chromatography. A》2003,988(2):277-284
We used the Generalized Rank Annihilation Method (GRAM), a second-order calibration method, to quantify aromatic sulfonates in water with high-performance liquid chromatography (HPLC) when interferences coeluted with the analytes of interest. With GRAM, we can quantify in only two chromatographic analyses, one for a calibration sample and one for the unknown sample. The calculated concentrations were not statistically different to those obtained when the chromatographic separation of the unknown sample was modified in order to completely separate the analyte from the interferences before univariate calibration. With GRAM, the concentrations are determined much more quickly because a complete resolution is not required. 相似文献
8.
Time shift correction in second-order liquid chromatographic data with iterative target transformation factor analysis 总被引:4,自引:0,他引:4
Enric Comas R. Ana Gimeno Joan Ferr Rosa M. Marc Francesc Borrull F. Xavier Rius 《Analytica chimica acta》2002,470(2):607-173
When the generalized rank annihilation method (GRAM) is applied to liquid chromatographic data with diode-array detection, an important problem is the time shift of the peak of the analyte in the test sample. This problem leads to erroneous predictions. This time shift can be corrected if a time window is selected so that the chromatographic profile of the analyte in the test sample is trilinear with the peak of the analyte in the calibration sample. In this paper we present a new method to determine when this condition is met. This method is based on the curve resolution with iterative target transformation factor analysis (ITTFA). The calibration and test matrices are independently decomposed into profiles and spectra, and aligned before GRAM is applied. Here we study two situations: first, when the calibration matrix has one analyte and second, when it has two analytes. When the calibration matrix has two analytes, we selectively determine the time window for the analyte to be quantified. There were considerably fewer prediction errors after correction. 相似文献
9.
J. Doménech E. Brillas J. A. Garrido R. M. Rodríguez 《Monatshefte für Chemie / Chemical Monthly》1987,118(2):197-202
Viscosities and densities of lithium perchlorate solutions in different ethylene glycol-water compositions have been measured at 25.0 and 35.0 °C. From these data, the correspondingB-coefficients of theJones-Dole equation have been determined. TheB-value depends on the solvent composition and it reaches a maximum in the water-rich region. This behaviour is analysed in terms of ionic solvation and solvent structure.
Viskositäts-B-Koeffizienten für Lösungen von Lithiumperchlorat in Ethylenglykol-Wasser-Mischungen
Zusammenfassung Es wurden die Dichten und Viskositäten für Lösungen von Lithiumperchlorat in verschieden zusammengesetzten Ethylenglykol-Wasser-Mischungen bei 25 °C und 35 °C gemessen. Auf Grund der erhaltenen Daten wurden dieB-Koeffizienten in den entsprechendenJones-Dole-Gleichungen für die relative Viskosität bestimmt. DieB-Werte hängen von der Zusammensetzung des Lösungsmittels ab und erreichen im wasserreichen Konzentrationsgebiet ein Maximum. Dieses Verhalten wird in Hinblick auf die Ionensolvatation und die Struktur des Lösungsmittels analysiert.相似文献
10.
The usefulness of qualitative and quantitative theoretical approaches in solid state chemistry is discussed by considering three different types of problems: (a) the distribution of boron and carbon atoms in MB2C2 (M=Ca, La, etc.) phases, (b) the band structure and Fermi surface of low-dimensional transition metal oxides and bronzes, and (c) the correlation between the crystal and electronic structure of the ternary nitride Ca2AuN. 相似文献