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121.
Kim HJ Kim H Alhakimi G Jeong EJ Thavarajah N Studnicki L Koprianiuk A Lough AJ Suh J Chin J 《Journal of the American Chemical Society》2005,127(47):16370-16371
Crystal structure and activation entropy data indicate that H-bond directed diaza-Cope rearrangement of chiral diimines takes place with a high degree of preorganization. CD spectroscopy and HPLC data show that there is inversion of stereochemistry for the reaction with excellent enantioselectivity. 相似文献
122.
Sec13p has been known as an endoplasmic reticulum-Golgi transport protein. Recently, it has also been shown to be required for the formation of septation in the fission yeast Schizosaccharomyces pombe. In the present study, we focused on the role of a human homolog of Saccharomyces cerevisiae SEC13, Sec13 protein during mitosis in U2OS cells. We found that the expression of Sec13 was constant throughout the cell cycle, and localized to the kinetochores at metaphase during mitosis. By using green fluorescent protein technology, we observed that Sec13 is required for evasion of mitotic arrest in response to spindle damage, leading to G1-like phase and apoptotic cell death. In addition, cells expressing exogenous Sec13 showed giant nuclei compared to endogenous ones in the absence of nocodazole. These results demonstrate that Sec13 is involved in the regulation of the metaphase/anaphase transition and may be functionally associated with mitotic machinery to maintain genomic stability during mitosis. 相似文献
123.
124.
Marten Van Dijk Dwaine Clarke Blaise Gassend G. Edward Suh Srinivas Devadas 《Designs, Codes and Cryptography》2006,39(2):253-273
We present protocols for speeding up fixed-base variable-exponent exponentiation and variable-base fixed-exponent exponentiation
using an untrusted computational resource. In the fixed-base protocols, the exponent may be blinded. In the variable-base
protocols, the base may be blinded. The protocols are described for exponentiation in a cyclic group. We describe how to extend
them to exponentiation modulo an integer where the modulus is the product of primes with single multiplicity. The protocols
provide a speedup of
over the square-and-multiply algorithm, where k is the bitlength of the exponent.
One application of the protocols is to speed up exponentiation-based verification in discrete log-based signature and credential
schemes. The protocols also allow signature verifiers to dynamically choose, for each message, the amount of work it would
like to perform to verify the signature. This results in a work-security tradeoff. We introduce a fifth protocol to perform
variable-base variable- exponent exponentiation, which also has this feature.
Our model allows the trusted resource to perform computations in its idle time. The protocols facilitate the offloading of
work to the offline stage, such that the work the trusted resource performs when it has to do an exponentiation is smaller.
Our protocols are unconditionally secure. 相似文献
125.
126.
T.S. Kim J.Y. Park T.V. Cuong H.J. Lee E.-K. Suh C.-H. Hong 《Journal of Crystal Growth》2004,270(3-4):340-345
The tri-methyl-Sb flow and the surfactant time dependence of photocurrent (PC) spectra was studied on InGaAsN/GaAs-strained multiple quantum wells (MQWs) structures grown by using metalorganic chemical vapor deposition (MOCVD). The structural properties of InGaAsN/GaAs-strained MQWs were investigated by using high-resolution X-ray diffraction (HRXRD). In the case of InGaAsN/GaAs-strained MQWs, an increase in compressive strain from an analysis of the satellite peaks in HRXRD was observed on increasing the tri-methyl-Sb flow and the surfactant time. For InGaAsN/GaAs-strained MQWs, the peaks observed in the photocurrent spectra were preliminarily assigned to electron–heavy hole (e1–hh) and electron–light hole (e1–lh) fundamental excitonic transitions. Their peaks are red-shifted with increasing tri-methyl-Sb flow and surfactant time. But the photocurrent peak is blue-shifted at the surfactant time of . It seems to be due to the improvement of structure properties at interface owing to a surfactant-suppressing surface diffusion phenomenon during growth. We compared this with the result of the experimental energies for InGaAsN/GaAs-strained MQWs. 相似文献
127.
The complex, [Zn(L)(NCO)]Cl · 3H2O (1) (L = 3,14-dimethyl-2,6,13,17-tetraazatricyclo[14,4,01.18,07.12]docosane), has been synthesized and structurally characterized. 1 crystallizes in the monoclinic system, space group P21/n with a = 10.530(3), b = 9.315(2), c = 27.188(3) Å, = 92.58(1)°, V = 2664.1(9)Å3, and Z = 4. The zinc atom is in a distorted squarepyramidal environment with the four nitrogen atoms of the macrocycle and one nitrogen atom of the isocyanate ligand. 相似文献
128.
We present a facile and straightforward method to synthesize uniform poly(vinyl amine) hydrogel shells with excellent loading capability for active materials and controllable responsiveness to applied stimuli, providing tunable releasing properties. 相似文献
129.
130.
Novel blue emitters, oligo-MCPPs (tri-MCPP, tetra-MCPP, and penta-MCPP), have been synthesized and characterized. The introduction of cyclopenta[def]phenanthrene (CPP) units into the structure of oligo-MCPPs gave LEDs with high efficiency and pure blue emission. UV-visible absorption spectra of the thin films of these compounds appear at 333-354 nm, and their maximum PL emission at 416-447 nm. Multilayer organic EL devices with oligo-MCPPs as an emitting layer showed the turn-on voltage of about 4.8 V, the maximum brightness of 1076 cd/m2 (at 8.2 V), the maximum luminescence efficiency of 0.81 cd/A, and the CIE coordinates of (0.17, 0.14) with blue color. 相似文献