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71.
JPC – Journal of Planar Chromatography – Modern TLC - Direct bioautography performed with luminescence gene-tagged bacteria enables almost real-time detection of antimicrobial compounds... 相似文献
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73.
Algorithms for separable nonlinear least squares with application to modelling time-resolved spectra
Katharine M. Mullen Mikas Vengris Ivo H. M. van Stokkum 《Journal of Global Optimization》2007,38(2):201-213
The multiexponential analysis problem of fitting kinetic models to time-resolved spectra is often solved using gradient-based
algorithms that treat the spectral parameters as conditionally linear. We make a comparison of the two most-applied such algorithms,
alternating least squares and variable projection. A numerical study examines computational efficiency and linear approximation
standard error estimates. A new derivation of the Fisher information matrix under the full Golub-Pereyra gradient allows a
numerical comparison of parameter precision under variable projection variants. Under the criteria of efficiency, quality
of standard error estimates and parameter precision, we conclude that the Kaufman variable projection technique performs well,
while techniques based on alternating least squares have significant disadvantages for application in the problem domain. 相似文献
74.
Separable routing is the first of a number of routing schemes for circuit switched telephone traffic invented at Bellcore. These routing schemes are state dependent, in the sense that, for each call attempt, a routing decision is made on the basis of the state of the network (defined in terms of the numbers of busy and idle trunks in the various trunk groups at the moment of the call attempt). In this paper, we describe separable routing and its mathematical background. Simulation results we have presented elsewhere show that the family of state-dependent routing schemes, of which separable routing is a member, is very attractive in terms of blocking rate, built-in network management features, and behavior in the presence of traffic forecast error. 相似文献
75.
The Green function for the mixed problem for the linear Stokes system in domains in the plane
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We construct the Green function for the mixed boundary value problem for the linear Stokes system in a two‐dimensional Lipschitz domain. 相似文献
76.
77.
Lehenmeier MW Bruckmeier C Klaus S Dengler JE Deglmann P Ott AK Rieger B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(32):8858-8869
The homogeneous dinuclear zinc catalyst going back to the work of Williams et al. is to date the most active catalyst for the copolymerisation of cyclohexene oxide and CO2 at one atmosphere of carbon dioxide. However, this catalyst shows no copolymer formation in the copolymerisation reaction of propylene oxide and carbon dioxide, instead only cyclic carbonate is found. This behaviour is known for many zinc‐based catalysts, although the reasons are still unidentified. Within our studies, we focus on the parameters that are responsible for this typical behaviour. A deactivation of the catalyst due to a reaction with propylene oxide turns out to be negligible. Furthermore, the catalyst still shows poly(cyclohexene carbonate) formation in the presence of cyclic propylene carbonate, but the catalyst activity is dramatically reduced. In terpolymerisation reactions of CO2 with different ratios of cyclohexene oxide to propylene oxide, no incorporation of propylene oxide can be detected, which can only be explained by a very fast back‐biting reaction. Kinetic investigations indicate a complex reaction network, which can be manifested by theoretical investigations. DFT calculations show that the ring strains of both epoxides are comparable and the kinetic barriers for the chain propagation even favour the poly(propylene carbonate) over the poly(cyclohexene carbonate) formation. Therefore, the crucial step in the copolymerisation of propylene oxide and carbon dioxide is the back‐biting reaction in the case of the studied zinc catalyst. The depolymerisation is several orders of magnitude faster for poly(propylene carbonate) than for poly(cyclohexene carbonate). 相似文献
78.
A series of mono-, bis- and trisnaphthalimides with different substituents on the naphthalimide ring system was prepared. For compounds containing a thiophenyl substituent fluorescence spectroscopic measurements were performed and unexpectedly showed an increase in fluorescence emission for the bis- and trisnaphthalimide derivatives in phosphate buffered saline. Additional fluorescence microscopic experiments indicated an efficient cellular uptake of the thiophenyl substituted compound 1c into cultured tumor cells. Experiments on the inhibition of tumor cell proliferation were performed in MCF-7 breast adenocarcinoma and HT-29 colon carcinoma cells and confirmed derivatives containing a nitro substituent as the most active compounds. Compound 1c demonstrated potential as photoinducable antitumor agent. 相似文献
79.
Picosecond time-resolved photoelectron spectroscopy is used to investigate intramolecular vibrational redistribution (IVR) following excitation of S(1) 18a(1) in p-fluorotoluene (pFT) at an internal energy of 845 cm(-1), where ν(18a) is a ring bending vibrational mode. Characteristic oscillations with periods of 8 ps and 5 ps are observed in the photoelectron signal and attributed to coupling between the initially excited zero-order bright state and two doorway states. Values for the coupling coefficients connecting these three vibrational states have been determined. In addition, an exponential change in photoelectron signal with a lifetime of 17 ps is attributed to weaker couplings with a bath of dark states that play a more significant role during the latter stages of IVR. A tier model has been used to assign the most strongly coupled doorway state to S(1) 17a(1) 6a(2)('), where ν(17a) is a CH out-of-plane vibrational mode and 6a(2)(') is a methyl torsional level. This assignment signifies that a torsion-vibration coupling mechanism mediates the observed dynamics, thus demonstrating the important role played by the methyl torsional mode in accelerating IVR. 相似文献
80.
Vanadyl ion substituted LiFePO(4) cathodes of the form LiFe(1-x)(VO)(x)PO(4) for 0 ≤ x ≤ 0.25 have been synthesized by a rapid microwave-solvothermal process at <300 °C within 10 min. Clear evidence of vanadyl ion substitution is demonstrated, despite a large size difference between Fe(2+) and (VO)(2+), by characterizing the products structurally, spectroscopically, and electrochemically. The vanadyl ion substitution is accompanied by the formation of iron vacancies in the lattice and Fe(3)O(4) impurity phase, which increases with increasing (VO)(2+) substitution for Fe(2+) and could be removed with a magnetic stir bar. The formation of iron vacancies, along with the oxidation of some Fe(2+) to Fe(3+) to maintain charge neutrality, results in a decrease in the unit cell volume with increasing x despite the substitution of larger (VO)(2+) for Fe(2+). Charge-discharge data of the vanadyl ion substituted samples suggest suppression of the two-phase plateau behavior that is characteristic of LiFePO(4). Electrochemical data collected without any carbon coating reveal that the capacity and rate capability decreases, but the capacity retention improves with (VO)(2+) substitution. 相似文献