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The problem of the calculation and interpretation of the net retention volume with a real gas as carrier is revisited. The properties of the carrier are described by a first order virial equation of state. The net retention volume of a solute is related to the mean flow rate of the carrier, therefore determination of the mean flow rate of a real gas carrier is reviewed. It is shown that the mean flow rate cannot be calculated from the mean column pressure. With a real gas carrier the local capacity factor depends on the local pressure of the real gas. The basic relationship between the net retention volume and the function describing this pressure dependence is also reviewed. Precise formulae as well as practical approximations are presented for the calculation of the mean flow rate, of the mean column pressure, and of a representative pressure related to the mean capacity factor. 相似文献
33.
Fluorescence and photodissociation of rhodamine 575 cations in a quadrupole ion trap 总被引:1,自引:1,他引:0
Sassin NA Everhart SC Dangi BB Ervin KM Cline JI 《Journal of the American Society for Mass Spectrometry》2009,20(1):96-104
The fluorescence and photodissociation of rhodamine 575 cations confined to a quadrupole ion trap are observed during laser irradiation at 488 nm. The kinetics of photodissociation is measured by time-dependent mass spectra and time-dependent fluorescence. The rhodamine ion signal and fluorescence decay are studied as functions of buffer gas pressure, laser fluence, and irradiation time. The decay rates of the ions in the mass spectra agree with decay rates of the fluorescence. Some of the fragment ions also fluoresce and further dissociate. The photodissociation rate is found to depend on the incident laser fluence and buffer gas pressure. The implications of rapid absorption/fluorescence cycling for photodissociation of dye-labeled biomolecular ions under continuous irradiation are discussed. 相似文献
34.
We study the minimum number of weights assigned to the edges of a graph G with no component K2 so that any two adjacent vertices have distinct sets of weights on their incident edges. The best possible upper bound on this parameter is proved. 相似文献
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Vincent J. Ervin Hyesuk Lee 《Numerical Methods for Partial Differential Equations》2006,22(1):145-164
We study a defect correction method for the approximation of viscoelastic fluid flow. In the defect step, the constitutive equation is computed with an artificially reduced Weissenberg parameter for stability, and the resulting residual is corrected in the correction step. We prove the convergence of the defect correction method and derive an error estimate for the Oseen‐viscoelastic model problem. The derived theoretical results are supported by numerical tests for both the Oseen‐viscoelastic problem and the Johnson‐Segalman model problem. © 2005 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq, 2006 相似文献
38.
The energetics and dynamics of collision-induced dissociation of O2- with Ar and Xe targets are studied experimentally using guided ion-beam tandem mass spectrometry. The cross sections and the collision dynamics are modeled theoretically by classical trajectory calculations. Experimental apparent threshold energies are 2.1 and 1.1 eV in excess of the thermochemical O2- bond dissociation energy for argon and xenon, respectively. Classical trajectory calculations confirm the observed threshold behavior and the dependence of cross sections on the relative kinetic energy. Representative trajectories reveal that the bond dissociation takes place on a short time scale of about 50 fs in strong direct collisions. Collision-induced dissociation is found to be remarkably restricted to the perpendicular approach of ArXe to the molecular axis of O2-, while collinear collisions do not result in dissociation. The higher collisional energy-transfer efficiency of xenon compared with argon is attributed to both mass and polarizability effects. 相似文献
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Summary A colorimetric method for the miorodetermination ofp-aminophenol based on indophenol dye formation is described. The conditions for its determination in the presence of theo- andm-isomers are given.
Zusammenfassung Eine kolorimetrische Methode für die Mikrobestimmung von p-Aminophenol, die auf der Bildung eines Indophenolfarbstoffs beruht, wurde beschrieben. Die Bedingungen für die Bestimmung in Anwesenheit der Ortho- und Meta-Isomeren wurden angegeben.
Résumé On décrit une méthode colorimétrique pour le microdosage dep-amino-phénole, basée sur la formation d'un colorant indophénolique. On donne les conditions du dosage en présence des isomères ortho et méta.相似文献
40.
Burke TJ Loniello KR Beebe JA Ervin KM 《Combinatorial chemistry & high throughput screening》2003,6(3):183-194
Fluorescence polarization technology has been used in basic research and commercial diagnostic assays for many decades, but has begun to be widely used in drug discovery only in the past six years. Originally, FP assays for drug discovery were developed for single-tube analytical instruments, but the technology was rapidly converted to high-throughput screening assays when commercial plate readers with equivalent sensitivity became available. This review will discuss fluorescence polarization assays in current use in drug discovery research as well as those in development that will likely be used in the near future. These assays include targets such as kinases, phosphatases, proteases, G-protein coupled receptors, and nuclear receptors. 相似文献