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31.
Manifestation of Ricci scalar like a matter field as well as a geometrical field, at high energy, has been noted earlier [9].
Here, its interaction with another scalar field is considered in four-dimensional curved space-time. This interaction leads
to the production of a large number of pairs of spinless particle-antiparticle due to expansion of the early universe in the
vacuum state (provided by temperature dependent Coleman-Weinberg like potential for Ricci field), where spontaneous symmetry
breaking takes place. 相似文献
32.
研究一维半导体在外电磁场中的光吸收、涉及电子带间的直接跃迁与间接跃迁,考虑了电子-空穴相互作用的激子光吸收,导出一维半导体的光吸收系数公式。 相似文献
33.
类比方法与光的本性的探索 总被引:2,自引:0,他引:2
简要回顾了人类对光的本性的探索历程,介绍了物理学家在研究过程中对类比方法的运用。 相似文献
34.
Interactive vortex shedding in the multiply connected domain formed by a pair of circular cylinders is analysed by the FEM–FDM blending technique. The vorticity–streamfunction formulation is used to solve the incompressible Navier–Stokes equations at Re = 100, with the time-dependent wall streamfunctions determined from the pressure constraint condition and the far-field streamfunctions from the integral series formula developed earlier by the authors. The standard Galerkin finite element method is used in the relatively small FEM subdomain and the finite difference method based on the general co-ordinate system in the rest of the flow domain. Symmetric, antisymmetric and asymmetric wake patterns are obtained confirming the earlier experimental findings. The bistable nature of the asymmetric vortex shedding as well as the intermittent drifting from one status to the other between symmetric and antisymmetric wake patterns are reported. 相似文献
35.
Hyoung Wook Moon 《Tetrahedron letters》2010,51(21):2906-380
The catalytic enantioselective conjugate addition reaction of α-nitroacetate to α,β-unsaturated ketones promoted by chiral bifunctional organocatalysts is described. The treatment of α-nitroacetate to α,β-unsaturated ketones under aqueous-phase reaction conditions afforded the corresponding Michael adducts with high enantioselectivity. The conjugate addition adducts are easily converted to chiral δ-keto nitroalkanes and δ-keto esters. 相似文献
36.
《Journal of Coordination Chemistry》2012,65(14):2376-2392
AbstractThioureas are important building blocks in medicinal chemistry; ferrocenes as highly hydrophobic moieties induce very interesting qualities in medicinal compounds. In this article, we have synthesized four ferrocene incorporated N,N′-disubstituted benzoyl thioureas (3a–3d) with general formula C5H5-Fe-C5H4C6H4Cl-NH-CS-NH-CO-C6H4(H/CH3). Molecular structures of these compounds were characterized in solid and solution phases. In solution molecular structures were established by 1H and 13C NMR and cyclic voltammetry. In the solid state their structures were characterized by elemental analyses and FTIR spectroscopy. Two of the compounds (3a and 3d) had also been structurally determined by single crystal X-ray diffraction analysis. The electrochemical characterization showed a reversible process with one electron transfer from Fe(II) to Fe(III). The single crystal analysis showed strong intermolecular non-covalent interactions in these compounds. Molecular structures of these compounds were also studied by density functional theory (DFT) calculation . DFT studies showed good correlation between calculated parameters and experimental results of solution phase and solid state characterizations. Compounds 3a–3d were evaluated for DNA interaction and antioxidant activity. These compounds interact with DNA via electrostatic forces and liberate significant binding constants and energies. Antioxidant potential –CSNH and –CONH groups induce same level of free radical scavenging ability in these compounds. 相似文献
37.
岩体具有复杂的内部结构,内部结构对于岩土的力学性质具有决定性的影响.文章从岩体结构层次的角度研究了岩体的动力变形与破坏过程,在松弛模型的框架内研究了变形破坏的空间尺度与应变率之间的关系.讨论了裂纹传播速度与荷载强度之间的关系,研究了岩体变形破坏的层次特性.最后从岩体结构层次角度研究了岩体的破坏准则.研究表明:岩体的动力变形与破坏具有层次特性,这一层次特性依赖于外载的空间与时间特性、岩体的结构层次和岩体变形与破坏过程速度的有限性.时间准则与极限变形准则可以较好地描述岩体的动力破坏. 相似文献
38.
Yongjie Chen;Yanwei Wang;Jun Nong;Dan Yuan;Yingming Yao; 《中国化学》2024,42(14):1571-1581
Eight zwitterionic rare earth metal complexes stabilized by amino-bridged tris(phenolato) ligands bearing quaternary ammonium side-arms were synthesized and characterized. These complexes were used as single-component catalysts for the cycloaddition of CO2 and epoxides, and their catalytic activities are obviously higher than those of their binary analogues. Further studies revealed that the halide anions (Cl–, Br–, I–) and the metal complexes influenced the catalytic activity, and the lanthanum complex bearing iodide anion showed the highest catalytic activity for this addition reaction. A variety of mono-substituted epoxides were converted to cyclic carbonates in good to excellent yields (55%—99%) with high selectivity (> 99%) at 30 °C and 1 bar CO2, whereas internal epoxides required higher both reaction temperatures (60—120 °C) and catalyst loading (2 mol%) for high yields. The catalyst was recyclable for four times without noticeable loss of catalytic activity. Based on the results of kinetic studies and in situ IR reactions, a plausible reaction mechanism was proposed. 相似文献
39.
Dr. Heng Xu Dr. Guanxing Xu Dr. Bingji Huang Dr. Jiabiao Yan Dr. Min Wang Prof. Lisong Chen Prof. Jianlin Shi 《Angewandte Chemie (International ed. in English)》2023,62(20):e202218603
Electricity generation and chemical productions are both critically important for the sustainable development of modern civilization. Here, a novel bifunctional Zn-organic battery has been established for the concurrent enhanced electricity output and semi-hydrogenations of a series of biomass aldehyderivatives, for the high value-added chemical syntheses. Among them, the typical Zn-furfural (FF) battery equipped with Cu foil-supported edge-enriched Cu nanosheets as cathodic electrocatalyst (Cu NS/Cu foil), provides a maximum current density and power density of 14.6 mA cm−2 and 2.00 mW cm−2, respectively, and in the meantime, produces high value product, furfural alcohol (FAL). The Cu NS/Cu foil catalyst exhibits excellent electrocatalytic performance of ≈93.5 % conversion ratio and ≈93.1 % selectivity for FF semi-hydrogenation at a low potential of -1.1 V vs. Ag/AgCl by using H2O as H source, and shows impressive performance for various biomass aldehyderivatives semi-hydrogenation. 相似文献
40.
Dr. Kuo Zhou Bixian Chen Xiaoting Zhou Dr. Shimin Kang Prof. Yongjun Xu Prof. Jinjia Wei 《ChemCatChem》2019,11(22):5562-5569
Effect of metal nature on reductive amination was investigated with biomass-based furfural as a typical substrate. Among the tested heterogeneous metal catalysts, cobalt proved to be the most effective metal for the synthesis of the corresponding primary amine. Under a relatively mild reaction condition, 98.9 % yield of furfurylamine was obtained over Raney Co and it can be reused more than eight times without a significant decrease in the catalytic performance. By extensively studying the catalytic pathways and reaction mechanism, it is found that the selectivity to primary amine and secondary amine was governed by the relative rate of hydrogenolysis and hydrogenation of the Schiff base intermediate. The superiority of Raney Co in furfurylamine synthesis can be ascribed to its high efficiency on hydrogenolysis of the Schiff base intermediate and its low performance in the hydrogenation of the Schiff base, carbonyl group and furan ring. Furthermore, ammonia greatly promoted the catalytic hydrogenolysis of the Schiff base intermediate over Raney Co without clear deactivation of the metal active sites. 相似文献