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961.
Quantum key distribution (QKD) is often, more correctly, called key growing. Given a short key as a seed, QKD enables two parties, connected by an insecure quantum channel, to generate a secret key of arbitrary length. Conversely, no key agreement is possible without access to an initial key. Here, we consider another fundamental cryptographic task, commitments. While, similar to key agreement, commitments cannot be realized from scratch, we ask whether they may be grown. That is, given the ability to commit to a fixed number of bits, is there a way to augment this to commitments to strings of arbitrary length? Using recently developed information-theoretic techniques, we answer this question in the negative. 相似文献
962.
Eichler C Bozyigit D Lang C Steffen L Fink J Wallraff A 《Physical review letters》2011,106(22):220503
A wide range of experiments studying microwave photons localized in superconducting cavities have made important contributions to our understanding of the quantum properties of radiation. Propagating microwave photons, however, have so far been studied much less intensely. Here we present measurements in which we reconstruct the quantum state of itinerant single photon Fock states and their superposition with the vacuum by analyzing moments of the measured amplitude distribution up to fourth order. Using linear amplifiers and quadrature amplitude detectors, we have developed efficient methods to separate the detected single photon signal from the noise added by the amplifier. From our measurement data we have also reconstructed the corresponding Wigner function. 相似文献
963.
For systems with a mixed phase space we demonstrate that dynamical tunneling universally leads to a fractional power law of the level-spacing distribution P(s) over a wide range of small spacings s. Going beyond Berry-Robnik statistics, we take into account that dynamical tunneling rates between the regular and the chaotic region vary over many orders of magnitude. This results in a prediction of P(s) which excellently describes the spectral data of the standard map. Moreover, we show that the power-law exponent is proportional to the effective Planck constant h(eff). 相似文献
964.
We discuss quantum fluctuations of the interface between a superfluid and a Mott-insulating state of ultracold atoms in a trap. The fluctuations of the boundary are due to a new type of surface modes, whose spectrum is similar--but not identical--to classical capillary waves. The corresponding quantum capillary length sets the scale for the penetration of the superfluid into the Mott-insulating regime by the proximity effect and may be on the order of several lattice spacings. It determines the typical magnitude of the interface width due to quantum fluctuations, which may be inferred from single-site imaging of ultracold atoms in an optical lattice. 相似文献
965.
Thomas Bose Steffen Trimper 《Physics letters. A》2011,375(24):2452-2455
A Lagrangian is introduced which includes the coupling between magnetic moments m and the degrees of freedom σ of a reservoir. In case the system-reservoir coupling breaks the time reversal symmetry the magnetic moments perform a damped precession around an effective field which is self-organized by the mutual interaction of the moments. The resulting evolution equation has the form of the Landau-Lifshitz-Gilbert equation. In case the bath variables are constant vector fields the moments m fulfill the reversible Landau-Lifshitz equation. Applying Noether?s theorem we find conserved quantities under rotation in space and within the configuration space of the moments. 相似文献
966.
Christensen H Schjøth-Eskesen C Jensen M Sinning S Jensen HH 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(38):10618-10627
We describe a novel approach for the synthesis of a series of 3,7-difunctionalised symmetric and unsymmetrical analogues of the tricyclic antidepressant (TCA) imipramine, which uses a key palladium-catalysed amination/cyclisation of an ester-functionalised dibromide. Of the ester, methyl, hydroxymethyl and methoxymethyl disubstituted compounds prepared, 3,7-dimethyl-imipramine was found to be the most potent against the human serotonin transporter (hSERT). The inhibitory potency of 3,7-dimethyl imipramine was found to be at least as high as the parent imipramine. This novel TCA also exhibits an increased selectivity (relative to imipramine) in binding to hSERT versus the human norepinephrine transporter (hNET). Even higher selectivity could be obtained with 3,7-dihydroxymethyl imipramine, which was found to be 167-fold more selective for hSERT over hNET, representative of a 120-fold gain in selectivity relative to the parent imipramine. These results further validate our previous model for the binding of imipramine and high-affinity analogues of imipramine to the central binding site of hSERT. 相似文献
967.
This study reports on a new method characterizing cellulose acetates and determining the contents of acetyl groups within
cellulose acetates based on FT Raman spectroscopy. Cellulose acetates exhibiting diverse degrees of substitution ascribed
to acetyl groups (DSAc) were obtained after the deacetylation of highly acetylated cellulose, i.e. cellulose diacetate and cellulose triacetate
(CTA), with aqueous sodium hydroxide solution or 1,6-hexamethylenediamine (HMDA). After plotting the Raman intensity ratios
between the bands at 1,740 and 1,380 cm−1 against the DSAc, a calibration curve with high correlation coefficient of more than 0.99 was obtained. During the deacetylation of highly
acetylated cellulose, a by-product—sodium acetate (NaOAc)—forms as the most possible salt among others. In order to determine
the content of NaOAc, the mixtures of cellulose acetates and NaOAc were measured with FT Raman spectroscopy. Based on the
relationship between the Raman intensity ratios as I929/I1380 and the contents of NaOAc in the mixtures, a calibration curve exhibiting high correlation coefficient of more than 0.99
was generated. 相似文献
968.
Repeatability standard deviation, laboratory standard deviation, and reproducibility standard deviation for quantitative methods
according to ISO 5725 series were recently proposed to estimate the precision of qualitative measurements, giving a presence/absence
response. In this paper, it is shown that for qualitative methods, the reproducibility standard deviation across laboratories
does not reflect the performance of the method as suggested. It is demonstrated that the benefit of the respective laboratory
standard deviation is very limited. Alternative performance measures are introduced which are based on another approach also
directly linked to ISO 5725. Thereby, meaningful information about the precision of qualitative test methods can be achieved. 相似文献
969.
Isomerization of trans-stilbenes is known to be induced by light. The two isomers have distinct absorption, fluorescence excitation and emission spectra. Resveratrol, 3,4',5-trihydroxystilbene, is a member of the stilbene family. The interest of the scientific community in resveratrol has increased over the last years due to its biomedical properties. Whereas there is a growing confidence that trans-resveratrol is non-toxic, very little is known about the pharmacology of cis-resveratrol. Of this very reason there is considerable interest in knowing the energetics of the trans-cis conversion. Cis-resveratrol is characterized by a large fluorescence quantum yield when compared to trans-resveratrol. In the present paper we report a detailed analysis of the spectral changes induced in trans-resveratrol upon 260?nm excitation for different time periods. Spectral changes have been monitored with UV-visible absorption and steady-state fluorescence spectroscopy at pH?4 at 20, 25, 30, 35, 40, 45 and 50?°C. Continuous 260?nm excitation induces a blue shift in the absorption and fluorescence excitation spectra of resveratrol and a 14?nm blue shift in its fluorescence emission. The photoisomerization yield is reported as a function of 260?nm excitation time. 330?min continuous excitation led to ~60% isomerization yield. The kinetics of trans-cis isomerization has been monitored following the increase in fluorescence quantum yield upon continuous 260?nm excitation of trans-resveratrol. The study was carried out at the above mentioned temperatures in order to obtain the Arrhenius activation energy of photoisomerization. Activation energy and pre-exponential factor were 3.7?±?0.3?kcal.mol(-1) and 10.6?±?1.6 s(-1), respectively. The activation energy is comparable with previously reported values for the photoisomerization of other stilbenes. 相似文献
970.