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71.
B.R. Lewis J.H. Carver T.I. Hobbs D.G. McCoy H.P.F. Gies 《Journal of Quantitative Spectroscopy & Radiative Transfer》1978,20(2):191-203
Experimental oscillator strengths and predissociated linewidths have been measured at room temperature for the (6-0)–(14-0) Schumann-Runge bands of molecular oxygen using the Adelaide 6 m vacuum u.v. monochromator operated at a resolution of about 0.06 Å. Photoelectric detectors were used to measure the u.v. absorption at two different gas pressures for 138 groups of rotational lines distributed throughout the (6-0)–(14-0) bands and the resulting data were interpreted using an equivalent width type of analysis. Experimental measurements of the variation with N″ of the oscillator strengths within each band have been obtained for the first time. Measured oscillator strengths are found to be somwhat higher in general than previously reported values with a slightly faster decrease as N″ increases than is predicted theoretically. The mean predissociated linewidths obtained for each band show a smooth variation with v′, agreeing well with other results for v′=12?14 and lying between previously reported experimental and theoretical values for v′=6?9. The present work provides results which can be used to construct highly accurate synthetic absorption profiles for studies of the atmospheric absorption of u.v. radiation by the Schumann-Runge bands. 相似文献
72.
The Kanai model of a quantum mechanical Brownian particle is used to examine the effect of interactions between particles and their environment. Random forces cause the thermalization of the particle. Reflection of a particle from a step barrier is analyzed. The problem of tunneling of the Brownian particle through a rectangular barrier is solved. Finally, a solution for a Brownian particle in a box is presented. 相似文献
73.
We construct the one-parameter family of solutions to d2w/dzsu2 = zw + 2w3 that tend to zero for z → +∞ by specializing an equation previously solved in connection with the two-dimensional Ising model. These solutions are intimately related to the KdV equation. 相似文献
74.
The identification of general principles relating structure to dynamics has been a major goal in the study of complex networks. We propose that the special case of linear network dynamics provides a natural framework within which a number of interesting yet tractable problems can be defined. We report the emergence of modularity and hierarchical organization in evolved networks supporting asymptotically stable linear dynamics. Numerical experiments demonstrate that linear stability benefits from the presence of a hierarchy of modules and that this architecture improves the robustness of network stability to random perturbations in network structure. This work illustrates an approach to network science which is simultaneously structural and dynamical in nature. 相似文献
75.
We demonstrate for the six vertex and XXZ model parameterized by = –(q+q-1)/2±1 that when q2N=1 for integer N2 the Bethe's ansatz equations determine only the eigenvectors which are the highest weights of the infinite dimensional sl2 loop algebra symmetry group of the model. Therefore in this case the Bethe's ansatz equations are incomplete and further conditions need to be imposed in order to completely specify the wave function. We discuss how the evaluation parameters of the finite dimensional representations of the sl2 loop algebra can be used to complete this specification. 相似文献
76.
In a recent paper published in Philosophical Magazine [Z.-D. Zhang, Phil. Mag. 87 (2007) p.5309], the author advances a conjectured solution for various properties of the three-dimensional Ising model. Here, we disprove the conjecture and point out the flaws in the arguments leading to the conjectured expressions. 相似文献
77.
Sheps L Miller EM Horvath S Thompson MA Parson R McCoy AB Lineberger WC 《The Journal of chemical physics》2011,134(18):184311
A combined experimental and theoretical investigation of photodissociation dynamics of IBr(-) and IBr(-)(CO(2)) on the B ((2)Σ(1/2)(+)) excited electronic state is presented. Time-resolved photoelectron spectroscopy reveals that in bare IBr(-) prompt dissociation forms exclusively I? + Br(-). Compared to earlier dissociation studies of IBr(-) excited to the A' ((2)Π(1∕2)) state, the signal rise is delayed by 200 ± 20 fs. In the case of IBr(-)(CO(2)), the product distribution shows the existence of a second major (~40%) dissociation pathway, Br? + I(-). In contrast to the primary product channel, the signal rise associated with this pathway shows only a 50 ± 20 fs delay. The altered product branching ratio indicates that the presence of one solvent-like CO(2) molecule dramatically affects the electronic structure of the dissociating IBr(-). We explore the origins of this phenomenon with classical trajectories, quantum wave packet studies, and MR-SO-CISD calculations of the six lowest-energy electronic states of IBr(-) and 36 lowest-energy states of IBr. We find that the CO(2) molecule provides sufficient solvation energy to bring the initially excited state close in energy to a lower-lying state. The splitting between these states and the time at which the crossing takes place depend on the location of the solvating CO(2) molecule. 相似文献
78.
Vogelhuber KM Wren SW Shaffer CJ McMahon RJ McCoy AB Lineberger WC 《The Journal of chemical physics》2011,135(20):204307
We report the 364-nm photoelectron spectrum of HC(4)N(-). We observe electron photodetachment from the bent X(2)A" state of HC(4)N(-) to both the near-linear X(3)A" and the bent ? (1)A' states of neutral HC(4)N. We observe an extended, unresolved vibrational progression corresponding to X(3)A" ← X(2)A" photodetachment, and we measure the electron affinity (EA) of the X(3)A" state of HC(4)N to be 2.05(8) eV. Photodetachment to the bent ? (1)A' state results in a single intense origin peak at a binding energy of 2.809(4) eV, from which we determine the singlet-triplet splitting (ΔE(ST)) of HC(4)N: 0.76(8) eV. For comparison and to aid in the interpretation of the HC(4)N(-) spectrum, we also report the 364-nm photoelectron spectra of HCCN(-) and DCCN(-). Improved signal-to-noise over the previous HCCN(-) and DCCN(-) photoelectron spectra allows for a more precise determination of the EAs and ΔE(ST)s of HCCN and DCCN. The EAs of HCCN and DCCN are measured to be 2.001(15) eV and 1.998(15) eV, respectively; ΔE(ST)(HCCN) is 0.510(15) eV and ΔE(ST)(DCCN) is 0.508(15) eV. These results are discussed in the context of other organic carbene chains. 相似文献
79.
H.P.F. Gies S.T. Gibson D.G. McCoy A.J. Blake B.R. Lewis 《Journal of Quantitative Spectroscopy & Radiative Transfer》1981,26(6):469-481
Experimental oscillator strengths and predissociation linewidths have been derived from equivalent width measurements at room temperature for the (11-0) to (15-0) Schumann-Runge bands of molecular oxygen, and at low temperature for the (15-0) to (19-0) bands, using the Adelaide 6 m vacuum ultraviolet monochromator operated at a resolution of 0.006 nm. Photometric methods were used to measure the ultraviolet absorption for 40 groups of ratational lines, and the resulting data were interpreted using a curve of growth type of analysis to give oscillator strengths and pre-dissociation linewidths. The variation of the oscillator strengths with N? within each band was found to agree well with the theoretical predictions of Allison, while the mean band oscillator strengths derived from the results are in good agreement with previous measurements. The results demonstrate the need for accurate data about multiplet line splittings. A revised analysis of previous data for the (7-0) to (14-0) bands is also presented. 相似文献
80.