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11.
The alkaline-earth group was isolated, after removal of silica, by precipitation as sulfates from an alcoholic solution. Those sulfates were reduced and dissolved by treatment with hydriodic acid. The alkaline earths were separated from each other by ion-exchange chromatography. The results are in good agreement with the values reported by the National Bureau of Standards. 相似文献
12.
The compounds 1,1,1-trichloro-2,4-pentanedione, Cu(II)tca2, Co(II)tca2, Mn(II)tca2, Al(III)tca3, Cr(III)tca3 and Fe(III)tca3 (tca?1,1,1-trichloro-2,4-pentanedionato, [CCl3COCHCOCH3]?) have been prepared and their mass spectra have been obtained. The mass spectral results have been compared with findings for comparable fluorinated and nonhalogenated compounds. Comparisons are made in terms of internal redox reactions and hard and soft acid base theory. Rearrangement of chloride from ligand to metal accompanied by the elimination of CO or other neutral even electron fragments emerges as an important reaction for the ions of these compounds. While the internal redox reactions characteristic of all previous β-diketonate complex mass spectra still occur, their importance appears reduced to some degree by the facility of the chlorine rearrangement. 相似文献
13.
Khuloud Takrouri Israel Goldberg Morris Srebnik 《Journal of organometallic chemistry》2005,690(18):4150-4158
The first examples of diborane (4) compounds derived from amine cyanoboranes are described. A series of monobromo derivatives of amine cyanoboranes (A:BHBrCN), and dibromo derivatives (A:BBr2CN), 1-7, were prepared. Lithiation of the monobromo derivative of trimethylamine cyanoborane, using n-BuLi, did not produce the C-lithiated intermediate Li+ [CH2NMe2BHBrCN]−, but instead the B-lithiated intermediate Li+ [Me3NBHCN]−, was obtained. This intermediate, when allowed to react for 16 h, coupled with the un-lithiated trimethylamine monobromocyanoborane (Me3NBHBrCN) and resulted in diborane (4) derivative formation as the 2LiBr complex. The same result was obtained when one equiv of the trimethylamine monobromocyanoborane was added to the reaction mixture 1 h after lithiation. Following the same procedure, novel diborane (4) derivatives of amine cyanoboranes were successfully obtained, 8-11, as their 2LiBr complexes from the monobromo derivatives of the corresponding amine cyanoboranes. Molecular structures of the trimethylamine dibromocyanoborane, 6, and the triethylamine dibromocyanoborane, 7, were determined using X-ray crystallography. 相似文献
14.
15.
16.
R. F. Kiefl J. Sonier D. A. Bonn J. H. Brewer J. F. Carolan K. H. Chow P. Dosanjh W. N. Hardy Ruixing Liang W. A. MacFarlane P. Mendels G. D. Morris T. M. Riseman J. W. Schneider 《Hyperfine Interactions》1994,86(1):537-542
We report precision transverse fieldSR measurements of the internal field distribution in the vortex state of crystalline YBa2Cu3O6.95. A novel low background apparatus was used to study a mosaic sample of three high quality single crystals (Tc=93.3K). The observed frequency spectra in magnetic fields of 5kG and 15 kG applied along the c-axis have the characteristic features expected for a regular vortex lattice with some additional broadening. From a preliminary analysis we find that [(0)/(T)]2 has a linear temperature coefficient forT<30 K. Such a term is inconsistent with simple s-wave pairing in the superconducting state. These results support recent microwave measurements of(T) on similar crystals in zero applied field but differ significantly from previousSR reports on sintered powders and crystals with lower Tc.This research was supported by the Natural Sciences and Engineering Research Council of Canada. 相似文献
17.
We present theS
1 Raman spectra of 1,4-DiPhenyl-1,3-Butadiene (DPB) in a series of linear alkanes (pentane, hexane, heptane, octane, decane, and dodecane). Bands assignable to both the 11
B
u
and 21
A
g
states are present, suggesting that the state we are observing in solution is a mixed state with both 11
B
u
and 21
A
g
character. The relative intensities of several bands associated with CoCo stretching motions in the 21
A
g
and 11
B
u
states change systematically through the solvent series. The relative intensity changes reflect a changing distribution ofs-trans conformers inS
1 DPB as the solvent is varied. We suggest that the distribution ofs-trans conformers inS
1 DPB controls the nature of the mixing between the 21
A
g
and 11
B
u
states and that the distribution of conformers is controlled by the solvent viscosity. Changes in the peak position and bandwidth of the phenyl C=C stretch with delay reflect vibrational relaxation processes inS
1 DPB. We observe anomolous behavior in pentane that we attribute to the effect of the solvent structure on the ability of DPB to exchange energy with pentane. 相似文献
18.
Espy MA Dehnhard D Edwards CM Palarczyk M Langenbrunner JL Davis B Burleson GR Blanchard S Gibbs WR Lail B Nelson B Park BK Zhao Q Cummings WJ Delheij PP Jennings BK Henderson R Häusser O Thiessen D Brash E Jones MK Larson B Brinkmöller B Maeda K Morris CL O'Donnell JM Penttilä S Swenson D Tupa D Bennhold C Kamalov SS 《Physical review letters》1996,76(20):3667-3670
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