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111.
112.
Extracellular biosynthesis of monodispersed gold nanoparticles by a SAM capping route 总被引:1,自引:0,他引:1
Li Wen Zhonghua Lin Pingying Gu Jianzhang Zhou Bingxing Yao Guoliang Chen Jinkun Fu 《Journal of nanoparticle research》2009,11(2):279-288
Monodispersed gold nanoparticles capped with a self-assembled monolayer of dodecanethiol were biosynthesized extracellularly
by an efficient, simple, and environmental friendly procedure, which involved the use of Bacillus megatherium D01 as the reducing agent and the use of dodecanethiol as the capping ligand at 26 °C. The kinetics of gold nanoparticle
formation was followed by transmission electron microscope (TEM) and UV-vis spectroscopy. It was shown that reaction time
was an important parameter in controlling the morphology of gold nanoparticles. The effect of thiol on the shape, size, and
dispersity of gold nanoparticles was also studied. The results showed that the presence of thiol during the biosynthesis could
induce the formation of small size gold nanoparticles (<2.5 nm), hold the shape of spherical nanoparticles, and promote the
monodispersity of nanoparticles. Through the modulation of reaction time and the use of thiol, monodispersed spherical gold
nanoparticles capped with thiol of 1.9 ± 0.8 nm size were formed by using Bacillus megatherium D01. 相似文献
113.
Zhang Zhonghua Wu Jianhua Suo Yaohong Zhang Juan 《Nonlinear Analysis: Real World Applications》2010,11(4):2422-2435
Considering the mechanism of quorum sensing, we formulate a bacteria-immunity model to describe the competition between bacteria and immune cells on the basis of Zhang’s model (see [9] for more details). A time delay is introduced to characterize the time in which bacteria receive signal molecules and then combat with immune cells. In the sequel, the length of delay which preserves the stability of the positive equilibrium is estimated, and the existence of Hopf bifurcation when the delay crosses through a critical value is investigated. Further, by using the normal form theory and center manifold theory, the explicit formulae are calculated which determine the stability, the direction and the period of bifurcating periodical solutions. Finally, numerical simulations are employed to verify the mathematical conclusions. 相似文献
114.
115.
Crown ethers and terpyridine ligands have been successfully attached to the focal point of light harvesting phenylacetylene monodendrons through Pd-catalyzed coupling reactions. The structures of these functional monodendrons were characterized by 1H and 13C NMR spectroscopy, mass spectrometry and elemental analysis. Such binding-ligand anchored dendrons exhibit broad absorption, large molar extenction coefficients and high fluoresence quantum yields. Coordination of crown ethers with alkali ions results in a significant increase in absorption strength in the UV range, but little alteration in either intensity or position of fluorescence emission. Coordination of terpyridine ligands with Ru2+, however, does efficiently quench the fluorescence from the dendrons,albeit only the smallest dendron exhibits efficient binding. 相似文献
116.
Discovery of a potent,selective protein tyrosine phosphatase 1B inhibitor using a linked-fragment strategy 总被引:3,自引:0,他引:3
Szczepankiewicz BG Liu G Hajduk PJ Abad-Zapatero C Pei Z Xin Z Lubben TH Trevillyan JM Stashko MA Ballaron SJ Liang H Huang F Hutchins CW Fesik SW Jirousek MR 《Journal of the American Chemical Society》2003,125(14):4087-4096
Protein tyrosine phosphatase 1B (PTP1B) is an enzyme that downregulates the insulin receptor. Inhibition of PTP1B is expected to improve insulin action, and the design of small molecule PTP1B inhibitors to treat type II diabetes has received considerable attention. In this work, NMR-based screening identified a nonselective competitive inhibitor of PTP1B. A second site ligand was also identified by NMR-based screening and then linked to the catalytic site ligand by rational design. X-ray data confirmed that the inhibitor bound with the catalytic site in the native, "open" conformation. The final compound displayed excellent potency and good selectivity over many other phosphatases. The modular approach to drug design described in this work should be applicable for the design of potent and selective inhibitors of other therapeutically relevant protein tyrosine phosphatases. 相似文献
117.
介绍了EAST托卡马克逆磁线圈加补偿线圈的逆磁测量。该方法的优点是补偿线圈有效地消除了纵场线圈产生的磁通变化,而调节机构能降低来自极向场的误差信号。详细地叙述了逆磁线圈工程设计中考虑的材料选择和结构设计对逆磁线圈的影响。最后给出了次测量系统的误差分析。 相似文献
118.
XI Shang-Zhong 《结构化学》2001,20(4)
1 INTRODUCTIONAtrope alkaloids, which exist in eggplant plants, such as atrope and scopolamine, are used as a series of important drugs in medical science [1,2]. The typical character of atrope alkaloid is that these compounds contain the main skeleton of 8-azabicycle[3,2,1]octane , which results in the very complicated synthetic routine[3]. During our research for the reaction of 1,3,5,7-tetraphenyl-4- nitro-1,7-heptadione with low-valent titanium reagent, we easily synthesized the title … 相似文献
119.
基于最小加速度原理的刚塑性动力问题 总被引:2,自引:0,他引:2
应用有限变形的最小加速度原理,推导出了小变形或有限变形构件受到刚性飞射物撞击时的刚塑性运动方程,指出该方法具有直接、简捷和可靠的特点。 相似文献
120.
掺铝的Ni(OH)2 通过共沉淀法制备,X射线粉末衍射法测定其晶体结构为α型层状结构. 用循环伏安法和恒流充放电法研究其电化学性能,实验结果表明掺铝镍电极具有比普通镍电极高得多的充放电容量,放电电位高80 m V. 相似文献