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991.
Hong Yu ZHANG* You Min SUN De Zhan CHEN Laboratory for Computational Biology Shandong Provincial Research Center for Bioinformatic Engineering Technique Shandong University of Technology Zibo Institute of Theoretical Chemistry Shand 《中国化学快报》2002,13(6)
In recent years, there has been growing interest in selecting efficient antioxidants with low toxicity to reduce the damage of free radicals. Among these antioxidants, flavonoids have been paid much attention, owing to their excellent antioxidative and pharmacological activities1. Up to now, many efforts have been given to summarize the structure-activity relationships (SAR) for flavonoids. It has been widely accepted that two structural factors are critical for flavonoids to enhance the… 相似文献
992.
Yan XingYunling Liu Zhan ShiPing Zhang Yunlong FuChang Cheng Wenqin Pang 《Journal of solid state chemistry》2002,163(2):364-368
A novel two-dimensional zinc phosphate Zn4P3O11(OH)·3CN2H4 in which the structure-directing organic amine acts as a ligand has been synthesized hydrothermally. The structure was solved by single-crystal X-ray diffraction analysis. Crystal data: triclinic, space group P1? (No. 2) with lattice parameters a=9.5663(15) Å, b=9.8530(16) Å, c=12.3658(19) Å, α= 77.495(4)°, β=77.893(4)°, γ=68.175(3)°, V=1045.6(3) Å3, Z=2, R1[I>2σ(I)]=0.0309, and wR2[I>2σ(I)]=0.0809. Interestingly the structure involves a network of ZnO4, PO4, PO3(OH), and the unusual ZnO3N and ZnO2N2 tetrahedra with shared vertices. There are 10-membered rings in the layers, in which the structure-directing imidazole molecules reside. The other amine molecules protrude from the Zn centers and occupy spaces between the layers. 相似文献
993.
Donzello MP Dini D D'Arcangelo G Ercolani C Zhan R Ou Z Stuzhin PA Kadish KM 《Journal of the American Chemical Society》2003,125(46):14190-14204
Following a previous report on the synthesis and physicochemical characterization of a novel class of porphyrazines carrying peripherally annulated seven-membered rings, i.e., tetrakis-2,3-(5,7-diphenyl-1,4-diazepino)porphyrazine [Ph(8)DzPzH(2)].4H(2)O and its metal derivatives [Ph(8)DzPzM].xH(2)O (x = 2-7, M = Mg(II)(H(2)O), Cu(II), and Zn(II)), a new more convenient procedure is reported here, allowing the preparation in high yields of the Li(I) and Na(I) derivatives of formulas [Ph(8)DzPzLi(2)].5H(2)O and [Ph(8)DzPzNa(2)].6H(2)O, which can be directly converted into other metal derivatives under mild conditions (room temperature) and in good yields. The series studied has been extended to include the Mn(II) and Co(II) complexes also reported here for the first time. Physicochemical characterization of the new "diazepinoporphyrazines" was based on fast atom bombardment (FAB) mass spectrometry and X-ray powder patterns, infrared (IR), electron paramagnetic resonance (EPR), and room-temperature magnetic susceptibility measurements. A detailed discussion of the UV-vis spectra emphasizes the role played by the external diazepine rings in electron delocalization through their tautomeric or protonated forms present in neutral, basic, and acidic media. The nonlinear optical effect of optical limiting for the different species [M = 2H, Mg(II)(H(2)O), Mn(II), Co(II), Cu(II), and Zn(II)] has also been measured. It has been observed that the extent of the optical limiting depends on the specific M center. The observed nonlinear optical features are analyzed and discussed in terms of the electronic and magnetic properties exhibited by some of the metal ions and taking into account the model of the excited-state absorption in which the nature of M determines the kinetics of formation of the highly absorbing state of the specific complex examined. As evidenced by the detailed electrochemical and spectroelectrochemical study carried out on this new class of macrocycles, one of the most important aspects is the facilitated electron delocalization for the oxidized and reduced species allowed by a 1H-6Htautomerism taking place on the peripheral diazepine rings. 相似文献
994.
Mei-Qin Zhan 《Mathematical Methods in the Applied Sciences》1997,20(8):679-688
This paper addresses the question: when the frequency of collisions vanishes, will the solutions of the Landau system converge to the solutions of the Vlasov system? We give a positive answer to the question for solutions satisfying certain regularity conditions. © 1997 by B. G. Teubner Stuttgart–John Wiley & Sons Ltd. Math. Meth. Appl. Sci., Vol. 20, 679–688 (1997). 相似文献
995.
本文研究了聚乙烯醇存在下,钛(Ⅳ)—氯磺酚S的显色反应,提出了用于硅酸盐矿中测微量钛的分光光度法。 相似文献
996.
合成了两种新聚合物冠醚,研究了它们对钠、钾离子络合容量和催化性能. 相似文献
997.
998.
Dongliang Zhan Joan Rose John B. Fenn 《Journal of the American Society for Mass Spectrometry》1998,9(12):1241-1247
Experiments are described in which bare (completely desolvated) ions are separated from their source gas and mixed with a bath gas of any desired temperature and precisely controlled composition. The resulting mixture of ions and bath gas is transported by free jet expansion into a vacuum system for mass analysis to reveal the extent to which the ions have formed adducts with other species in the bath gas. Because the ions are separated from their source gas or vapor before they are mixed with the bath gas, the compositions of the bath gas and source gas are completely independent. Thus, one can examine solvation or adduction by any desired species contained in the bath gas without any interference from other species that might be present in the source gas. Reported here are results obtained on the solvation of electrospray ions of a small peptide, leucine-enkephalin, by water and several alkanols. One provocative finding is that a substantial fraction of ions thought to be singly charged monomers turned out to be doubly charged dimers. 相似文献
999.
The reaction of heteroaroyl‐substituted heterocyclic ketene aminals with 2,3,4,6‐tetra‐O‐acetyl‐β‐D ‐glucopyranosyl azide was investigated and a series of potential bioactive compounds, 1‐glucopyranosyl‐4‐heterocyclic‐5‐heteroaryl‐1,2,3‐triazoles, were obtained in good yields. Both the reaction rate and the yield were strongly affected by the heteroaryl and heterocyclic groups. In order to improve their water solubility, the deprotection of 1‐glucopyranosyl‐4‐heterocyclic‐5‐heteroaryl‐1,2,3‐triazole was carried out. © 2002 Wiley Periodicals, Inc. Heteroatom Chem 13:242–247, 2002; Published online in Wiley Interscience (www.interscience.wiley.com). DOI 10.1002/hc.10023 相似文献
1000.