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991.
Hasse U Palm GJ Hinrichs W Schäfer J Scholz F 《Physical chemistry chemical physics : PCCP》2011,13(26):12254-12260
Single crystal silver wires can be grown at the nitrobenzene|water interface when silver ions dissolved in the aqueous phase are reduced by decamethyl ferrocene dissolved in the nitrobenzene phase. The successful growth of these wires depends on a number of experimental conditions, most prominently on the concentration ratio of reactants, nucleation rates, shape of formed nuclei, and wettability of nuclei. The size-time dependence can be modeled on the basis of microelectrode behavior of the silver nuclei and wire. AFM, SEM, light microscopy and single crystal X-ray diffraction has been applied to study the morphology of the silver nuclei and wires. 相似文献
992.
Köberl M Cokoja M Herrmann WA Kühn FE 《Dalton transactions (Cambridge, England : 2003)》2011,40(26):6834-6859
Metal-organic frameworks (MOF) are becoming a more and more important class of functional materials. Yet, very often, the synthesis of MOFs is not easy to control and requires a profound knowledge and experience in solid state chemistry. One of the most frequently used metal connectors is the so-called 'paddle-wheel' (PW) unit, which is a well-known molecular compound type in inorganic coordination chemistry. Depending on the ligands, the geometry of PWs strictly directs the assembly of ordered networks. This review focuses on the question, to what extent ordered network structures can be accessed by typical molecular syntheses in solution, starting from molecular PW complexes to ordered macromolecules, finite cage compounds and finally, three-dimensional superstructures. 相似文献
993.
Weisser F Huebner R Schweinfurth D Sarkar B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(20):5727-5736
Reactions of [{Ru(tmpa)}2(μ‐Cl)2][ClO4]2, ( 2 [ClO4]2, tmpa=tris(2‐pyridylmethyl)amine) with 2,5‐dihydroxy‐1,4‐benzoquinone ( L1 ), 2,5‐di‐[2,6‐(dimethyl)‐anilino]‐1,4‐benzoquinone ( L2 ), or 2,5‐di‐[2,4,6‐(trimethyl)‐anilino)]‐1,4‐benzoquinone ( L3 ) in the presence of a base led to the formation of the dinuclear complexes [{Ru(tmpa)}2(μ‐ L1 ?2 H)][ClO4]2 ( 3 [ClO4]2), [{Ru(tmpa)}2(μ‐ L2 ?2 H)][ClO4]2 ( 4 [ClO4]2), and [{Ru(tmpa)}2(μ‐ L3 ?2 H)][ClO4]2 ( 5 [ClO4]2). Structural characterization of 5 [ClO4]2 showed the localization of the double bonds within the quinonoid ring and a twisting of the mesityl substituents with respect to the quinonoid plane. Cyclic voltammetry of the complexes show two reversible oxidation and quinonoid‐based reduction processes. Results obtained from UV/Vis/NIR and EPR spectroelectrochemistry are invoked to discuss ruthenium‐ versus quinonoid‐ligand‐centered redox activity. The complex 3 [ClO4]2 is compared to the reported complex [{Ru(bpy)}2(μ‐ L1 ?2 H)]2+ ( 12+ , bpy=2,2′‐bipyridine). The effects of substituting the bidentate and better π‐accepting bpy co‐ligands with tetradentate tmpa ligands [pure σ‐donating (amine) as well as σ‐donating and π‐accepting (pyridines)] on the redox and electronic properties of the complexes are discussed. Comparisons are also made between complexes containing the dianionic forms of the all‐oxygen‐donating L1 ligand with the L2 and L3 ligands containing an [O,N,O,N] donor set. The one‐electron oxidized forms of the complexes show absorption in the NIR region. The position as well as the intensity of this band can be tuned by the substituents on the quinonoid bridge. In addition, this band can be switched on and off by using tunable redox potentials, making such systems attractive candidates for NIR electrochromism. 相似文献
994.
Elementary processes like energy transfer, charge transport, and exciton diffusion in thin films occur on time scales of femtoseconds. Time-resolved photo-electron spectroscopy, a technique limited to ultra-high vacuum environment and the proper choice of a substrate, has been used to study ultrafast processes in sub-nanometer thin films so far. Herein we show that a transient (population) grating created by the interference of laser pulses can be used to study ultrafast processes in such films under ambient conditions. Our investigations of exciton dynamics in 1.4±0.2 nm and 0.4±0.2 nm thin films, formed by nanocrystals of 3,4,9,10-Perylenetetracarboxylic dianhydride (PTCDA) on glass and mica, show that the dynamics differ with the crystal size, possibly due to the confinement induced changes in the electronic structure. The technique is sensitive enough to investigate the dynamics in systems, where only 20 % of the surface is covered by nano-crystals. We expect such an optical technique that is sensitive enough to study dynamics in few to sub-nanometer thin layers under ambient conditions to become important in investigating ultrafast dynamics on surfaces, interfaces, functionalized materials, organic semiconductors, and quantum phenomena in ordered structures of reduced dimensions, such as quantum dots and graphene sheets. 相似文献
995.
Canella D Hock SJ Hiltner O Herdtweck E Herrmann WA Kühn FE 《Dalton transactions (Cambridge, England : 2003)》2012,41(7):2110-2121
Nine new complexes of the type fac-[(CO)(3)ReBr(L)], where L represents a chelating bis-NHC ligand consisting of two alkylene (propylene and butylene) bridged (R') N-substituted (R) imidazoline moieties (1,1'-di-R-3,3'-R'-diimidazolin-2,2'-diylidene), were synthesized. Spectroscopic methods, elemental analysis, mass spectrometry and X-ray crystallography were employed to characterize the complexes both in solution and in solid state. The complexes were compared to the analogous complexes with smaller bridge lengths in order to reveal differences and similarities. Depending on the bridge length and the ligand size in some cases dinuclear complexes were obtained as small scale side products. 相似文献
996.
The oxidation of white phosphorus has been studied with graphite rods of varying diameters, which were partially embedded in solid white phosphorus placed on the bottom of a cell filled with aqueous electrolyte solution. During the first scan in linear sweep voltammetry, the current measured at various potentials is directly proportional to the length of the three-phase junction (tpj) line phosphorus|graphite|electrolyte solution. The currents are orders-of-magnitude larger than predicted for a reaction that is strictly confined to a tpj line of atomic size and length of 4–16 mm as used in the experiments. A model is presented which explains the reaction layer as built up of vitreous low-valent phosphorus oxides possessing electron hopping capabilities and ionic conductivity. It is assumed that the reaction starts at the tpj line, however, quickly converts to a reaction where electrons are transferred across an expanding face graphite|phosphorus oxides and where ions are transferred across an expanding face phosphorus oxides|electrolyte solution. 相似文献
997.
998.
999.
Daranciang D Highland MJ Wen H Young SM Brandt NC Hwang HY Vattilana M Nicoul M Quirin F Goodfellow J Qi T Grinberg I Fritz DM Cammarata M Zhu D Lemke HT Walko DA Dufresne EM Li Y Larsson J Reis DA Sokolowski-Tinten K Nelson KA Rappe AM Fuoss PH Stephenson GB Lindenberg AM 《Physical review letters》2012,108(8):087601
We show that light drives large-amplitude structural changes in thin films of the prototypical ferroelectric PbTiO3 via direct coupling to its intrinsic photovoltaic response. Using time-resolved x-ray scattering to visualize atomic displacements on femtosecond time scales, photoinduced changes in the unit-cell tetragonality are observed. These are driven by the motion of photogenerated free charges within the ferroelectric and can be simply explained by a model including both shift and screening currents, associated with the displacement of electrons first antiparallel to and then parallel to the ferroelectric polarization direction. 相似文献
1000.
We investigate how a magnetic field induces one-dimensional edge channels when the two-dimensional surface states of three-dimensional topological insulators become gapped. The Hall effect, measured by contacting those channels, remains quantized even in situations where the θ term in the bulk and the associated surface Hall conductivities, σ(xy)(S), are not quantized due to the breaking of time-reversal symmetry. The quantization arises as the θ term changes by ±2πn along a loop around n edge channels. Model calculations show how an interplay of orbital and Zeeman effects leads to quantum Hall transitions, where channels get redistributed along the edges of the crystal. The network of edges opens new possibilities to investigate the coupling of edge channels. 相似文献