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101.
T-2 toxin and diacetoxyscirpenol (DAS), two trichothecene mycotoxins containing one hydroxy group, have been volatilized by induction heating, revolatilized, and analyzed by gas chromatography (GC) and/or GC mass spectroscopy. Seventy to eighty percent of DAS was recovered by this system; 60–70% T-2 toxin was recovered. When the hydroxy group is derivatized by acetate, 90–100% recovery is obtained. Other trichothecenes of the macrocyclic ester type (e.g., Roridan A) were also tried. Ten to twenty percent of the macrocyclic ester was obtained without derivatization. 相似文献
102.
Gordon K. Anderson Ronald J. Cross Ljubica Manojlovic-Muir Kenneth W. Muir Tihomir Solomun 《Journal of organometallic chemistry》1979,170(3):385-397
The known complex, -(η-C5H5)2Rh2(CO)2(CF3C2CF3) is formed in high yield from (η-C5H5)Rh(CO)2 and CF3FCCF3 at 100°. The less stable -isomer of the complex is obtained in low yield from the same reaction. The infrared, 1H, 19F and 13C NMR spectra of the two isomers are compared. The -isomer undergoes CO scrambling in solution at room temperature, and the variable temperature 13C NMR spectra are consistent with a pairwise bridge opening and closing mechanism. The mechanism is extended to account for the isomerization of to isomer, whihc has a half-life of 12 h at room temperature. The 13C spectrum indicates that the -isomer is static in solution at room temperature. The -isomer is reversibly protonated by protonic acids, and BF4? and PF6? salts of the protonated species can be isolated. The spectroscopic properties of these salts are consistent with protonation at one of the alkynyl-carbons, but it is not possible to distinguish between two alternative structures for the complex cation.Treatment of (η-C5H5)2Rh2(CO)2(CF3C2CF3) with (η-C5H5)Rh(CO)2 gives the trinuclear complex (η-C5H5)3Rh3(CO)(CF3C2CF3) in 80% yield. The analogoug but-2-yne complex is formed from (η-C5H5)3Rh3(CO)3 and MeCCMe. The infrared, 1H, 19F and 13C NMR spectra indicate that the hexafluorobut-2-yne complex exists in two different structural arrangements in solution. One has an edge bridging, and the other a face bridging carbonyl. The proportion of the isomers is affected by the solvent polarity. The spectra of the but-2-yne complex indicate it is fluxional at room temperature, and has a face bridging structure in solution regardless of the polarity of the solvent. Reversible protonation of the hexafluorobut-2-yne complex occurs in protonic acids, and the salt [(η-C5H5)3Rh3(CO)(CF3C2CF3)H]+[BF4]?,H2O can be isolated. The spectroscopic properties of this complex are consistent with a structure incorporating an edge-bridging carbonyl, and probably, an edge-bridging hydride ligand. 相似文献
103.
Anodic stripping voltammetry at a glassy carbon disc electrode covered by a thin mercury film was adapted for use in a flow-through cell. The resulting system is characterized by extreme simplicity of set-up and operation, high sensitivity and excellent precision and stability. Its performance was tested via the determination of hydrated or labile complex ions of heavy metal ions in sea water, using short (2–10 min) deposition periods. The dependence of the stripping peak charge on metal ion concentration, length of deposition period, solution flow rate and other variables was examined and the reliability of the results obtained were evaluated under conditions resembling continuous monitoring. 相似文献
104.
Eric G. Bryan Brian F.G. Johnson Jack Lewis 《Journal of organometallic chemistry》1976,122(2):249-252
Treatment of H2Os3(CO)10 with cyclonona-l,2-diene produced HOs3(CO)9C9H13 and Os2(CO)6(C9H4)2. Single crystal X ray analysis has shown that the latter is not isostructural with Fe2(CO)6(C9H14)2. 相似文献
105.
Solubilities and the solvolytic behaviour of various inorganic compounds, Lewis acids and bases in fused monobromoacetic acid at 60 ± 0.5°C are discussed. Ionic compounds are fairly soluble, iodides and thiocyanates being comparatively more soluble than chlorides and bromides. Tetraalkyl ammonium halides are highly soluble in this solvent. Conductometric and spectroscopic studies of various Lewis acids and bases in fused monobromoacetic acid indicate their solvolytic behaviour and their subsequent ionization. The solvolyses products BBr3·CH2BrCOOH and SbCl5·CH2BrCOOH have been observed to be the strongest Bronsted acids. Auto-ionization of this solvent has been supported by acid/base titrations. 相似文献
106.
Experimental evidence for the existence of a Ramsauer—Townsend minimum in the electron scattering cross section for liquid CH4 and liquid Ar (Kr and Xe) is provided from: (i) comparisons of thermal electron mobilities in gases with those in liquids, (ii) changes in the electron mobility with gas density, and (iii) the dependence of the electron mobility on temperature for liquids whose V0, the energy of the electron state in the liquid, is ? 0 eV. 相似文献
107.
Crystals of Li0.33 MoO3 (blue), Rb0.23MoO3 (blue) and Cs0.31MoO3 (red) were grown by electrolysis from MoO3M2MoO4 melts (M =alkali metal) with composition 70–77 mole% MoO3. Melts richer in M2MoO4 produced MoO2 only. Correlation is made between bronze formation and the coordination of Mo in the melt and in the equilibrium solid phase M2Mo4O13. Li0.33MoO3 and Cs0.31MoO3 are semiconductors with high-temperature-range activation energies 0.16 and 0.12 eV. Rb0.23MoO3 has an electrical behavior similar to that of blue KxMoO3 with a semiconductor-metal transition at (170 ± 5) K. ESR spectra observed in Li0.33MoO3 and Rb0.23MoO3 single crystals at 4.2 K show extensive delocalization of the 4d1 electron associated with Mo(V) centers. Attempts to grow molybdenum bronzes containing Ca or Y were unsuccessful. 相似文献
108.
[H3O][Ce(SO4)2] · H2O crystallizes in the monoclinic system with unit-cell dimensions (from single-crystal data) a = 9.359(4), b = 9.926(4), c = 8.444(3) Å, β = 96.53(9)° and space group P21/n, z = 4. The structure was solved by conventional heavy-atom methods using 1787 counter-measured reflections (MoKα radiation), and refined using full-matrix least-squares techniques to an R of 0.0465 (ωR = 0.0413). The structure consists of cerium(III) ions in irregular nine-coordination to oxygen atoms from two bidentate sulfate ions, four monodentate sulfate oxygen atoms, and one water molecule. The oxonium ions are present as isolated ions in the structure and take par in the hydrogen bonding network. The Ce-O bond lengths range from 2.454(7) to 2.626(6) Å. 相似文献
109.
The ionic conductivity of polycrystalline pellets of Li2MgSn3O8 with ramsdellite-type structure was measured by complex impedance technique. The conductivity is 1.2 × 10?8 (Ω cm)?1 at 300°C and 2.3 × 10?4 (Ω cm)?1 at 450°C. The results are discussed in relation to structural properties. 相似文献
110.
The open circuit dissolution of ionic metal oxides in mineral acids is modelled assuming that the rate is controlled by the transfer of metal ions in hydrolytic equilibrium with bulk metal ions, from the metal oxide surface to the Stern plane. The site-binding model of the double layer metal oxide/electrolyte solution is used to obtain the pH dependence of surface and Stern potentials. The nature of the active sites is discussed and their surface concentration is assumed to be proportional to suface charge σ0. Again, the site-binding model is used to detemine the pH dependence of σ0. It is thus shown that the rate order in cH+ is essentially defined by the potential dependence of the charge transfer process, for oxides with points of zero charge near neutrality that dissolve in mildly or strongly acidic solutions. The role of surface complexation is also discussed in terms of the site-binding model and the difficulties in interpreting dissolution experiments under constant external applied potential are discussed in terms of the complexity of the semiconductor oxide/electrolyte solution interfacial region in magnetite.An experimental study of the open circuit dissolution of magnetite in sulfuric acid is presented and interpreted according to the proposed model.The reductive dissolution of magnetite is modelled by extension of the Valverde-Wagner model of oxide dissolution. Experimental results are presented to demonstrate that the reductive dissolution rate of magnetite in ferrous containing solutions is controlled by the rate of electron transfer from adsorbed Fe(II) to Fe(III) surface states of magnetite. 相似文献