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91.
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93.
G. Bruun Y. Castin R. Dum K. Burnett 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》1999,7(3):433-439
We develop an extension of the well-known BCS-theory to systems with trapped fermionic atoms. The theory fully includes the
quantized energy levels in the trap. The key ingredient is to model the attractive interaction between two atoms by a pseudo-potential
which leads to a well defined scattering problem and consequently to a BCS-theory free of divergences. We present numerical
results for the BCS critical temperature and the temperature dependence of the gap. They are used as a test of existing semi-classical
approximations.
Received 18 December 1998 相似文献
94.
OK Yoon WG Hwang JC Choe MS Kim 《Rapid communications in mass spectrometry : RCM》1999,13(14):1515-1521
A technique to investigate photodissociation kinetics on a nanosecond time scale has been devised for molecular ions generated by multiphoton ionization (MPI) using mass-analyzed ion kinetic energy spectrometry. The branching ratio or rate constant has been determined for the photodissociation of the n-butylbenzene, bromobenzene, iodobenzene, and aniline molecular ions generated by MPI at 266 nm. The ion internal energies have been estimated by comparing the measured kinetic data with the previous energy dependence data. The analysis has shown that only those molecular ions generated by two-photon ionization contribute to the photodissociation signals. Around half of the available energy has been found to remain as molecular ion internal energy in the two-photon ionization process. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
95.
Keith R. Burnett M.D. Edward J. Goldstein Ph.D. M.D. Gerald L. Wolf Ph.D. M.D. Swapan Sen B.S. R.T. R.D.M.S. Alex C. Mamourian M.D. 《Magnetic resonance imaging》1984,2(4):307-314
Mn+2 (as MnCl2) was administered to rabbits intravenously and orally (a route of administration which based upon our previous experiments in rats7 promises to give selective hepatobiliary enhancement with less systemic toxicity). Nuclear magnetic relaxation dispersion or T1 (NMRD) was performed on selected tissues (heart, liver, kidney, serum, and bile) in both animal groups to examine possible qualitative and semiquantitative differences in T1 relaxation at equivalent sacrifice times. One animal was given an oral dose of MnCl2 (620 micromoles/kg) and imaged sequentially (T1 weighted sequence, .12T) for 30 minutes. The NMRD curves for organ tissues show an increase in relaxation efficacy in the 10–20MHz range characteristic of Mn-macromolecular complexes and are similar irrespective of the route of administration. The lack of increased relaxation enhancement for bile in this frequency range reflects cleavage of this complex upon excretion. Decreased overall relaxation in the liver is observed when oral Mn+2 is compared to IV Mn+2 due to the small fraction of administered dose that is absorbed. However, the images document a significant increase in the intensity of liver signal after the oral dose. We suspect this dose may ultimately be adjusted downward to give selective hepatobiliary effects. 相似文献
96.
We present numerical results from a second-order quantum field theory of Bose-Einstein condensates applied to the 1997 JILA experiment [Phys. Rev. Lett. 78, 764 (1997)]]. Good agreement is found for the energies and decay rates for both the lowest-energy m=2 and m=0 modes. The anomalous behavior of the m=0 mode is due to experimental perturbation of the noncondensate. The theory is gapless and includes the coupled dynamics of the condensate and thermal cloud, the anomalous pair average, and all relevant finite size effects. 相似文献
97.
Non-exponential proton spin—lattice relaxation has been observed in solid CH3CH3 and CH3CD3. Comparison with recent theoretical predi 相似文献
98.
99.
L. J. Burnett C. L. Rottler D. H. Laughon 《Journal of Polymer Science.Polymer Physics》1978,16(2):341-347
Proton spin–lattice relaxation times T1 were measured for two samples of polydimethylsiloxane (PDMS), one with weight-average molecular weight Mw = 77,400 and the other with Mw = 609,000. Two T1 minima and a T1 discontinuity were observed for each compound. The high-temperature T1 minima were attributed to a stretching and flexing motion of the PDMS chain. Quantitative comparison of the relaxation data with a theoretical model developed for this motion allowed the activation energy, 2.3 kcal/mole, and the maximum angular displacement of the methyl group symmetry axis to be determined. The latter was found to be 31°, independent of sample molecular weight. The low-temperature minima were ascribed to methyl reorientation with an activation energy of 1.6 kcal/mole. The T1 discontinuities were attributed to melting and allowed the degree of crystallinity to be estimated. 相似文献
100.