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161.
Stefan G Ebbinghaus 《Journal of solid state chemistry》2004,177(3):817-823
Single crystals of the new compound La1.2Sr2.4RuO7, an oxide related to the hexagonal perovskites, were grown from a BaCl2 flux. The structure was solved by single crystal X-ray diffraction. La1.2Sr2.4RuO7 crystallizes in the space group with a=5.760(1) Å and c=18.273(3) Å. It is one of the rare examples of oxides with isolated RuO6-octahedra. The structure consists of alternating layers of RuO6-octahedra and trigonal (La,Sr)O6-prisms. These prisms are capped by one additional oxygen ion, which occupies a distorted position within the (La,Sr)O6-layers. La1.2Sr2.4RuO7 is the second member of the general [A2O][AnBn−1O3n] family of hexagonal perovskites with n=2 and the first ruthenate possessing this structure. XANES investigations, bond valence sum calculations and magnetic measurements show that ruthenium takes the oxidation state +5. Although the ruthenium ions have quite long distances, a medium strong antiferromagnetic interaction between these paramagnetic centers was observed. 相似文献
162.
163.
Synthesis and characterization of monodisperse magnetic composite particles for magnetorheological fluid materials 总被引:2,自引:0,他引:2
Jung-Bae Jun Seong-Yong Uhm Jee-Hyun Ryu Kyung-Do Suh 《Colloids and surfaces. A, Physicochemical and engineering aspects》2005,260(1-3):157-164
Monodisperse magnetic composite particles (MCP) were prepared and characterized for a study of magnetic field-responsive fluids. Magnetic composite particles used are iron oxide-coated polymer composite particles, which were synthesized through in situ coating of iron oxide onto pre-existing polymer particles by the reduction of ferrous fluids. For a uniform and bulk coating of iron oxide, the porous structure was introduced into the substrate polymer particles through a two-step seeded polymerization method. Moreover, surface cyano-functionality was born from acrylonitrile unit of substrate polymer and it played an important role in obtaining successful uniform coating. The structure of the composite particle was analyzed by using a thermo gravimetric analysis (TGA) and a X-ray diffraction (XRD) analysis. The magnetization property of the particle was also observed. Then, the rheological properties of monodisperse magnetorheological (MR) suspensions of magnetic composite particles were examined under a magnetic field using a parallel-plate type commercial rheometer. From the rheological measurements, it was found that MR properties of the magnetic composite suspensions are dependent on the iron oxide content and the fluid composition. 相似文献
164.
Properties of Sr2Cu(PO4)2 and Ba2Cu(PO4)2 having [Cu(PO4)2]∞ linear chains in their structures with Cu-O-P-O-Cu linkages were studied by magnetic susceptibility (T=2-400 K, H=100 Oe) and specific heat measurements (T=0.45-21 K). Magnetic susceptibility versus temperature curves, χ(T), showed broad maxima at TM=92 K for Sr2Cu(PO4)2 and TM=82 K for Ba2Cu(PO4)2 characteristic of quasi-one-dimensional systems. The χ(T) data were excellently fitted by the spin susceptibility curve for the uniform S=1/2 chain (plus temperature-independent and Curie-Weiss terms) with g=2.153(4) and J/kB=143.6(2) K for Sr2Cu(PO4)2 and g=2.073(4) and J/kB=132.16(9) K for Ba2Cu(PO4)2 (Hamiltonian H=JΣSiSi+1). The similar J/kB values were obtained from the specific heat data. No anomaly was observed on the specific heat from 0.45 to 21 K for both compounds indicating that the temperatures of long-range magnetic ordering, TN, were below 0.45 K. Sr2Cu(PO4)2 and Ba2Cu(PO4)2 are an excellent physical realization of the S=1/2 linear chain Heisenberg antiferromagnet with kBTN/J<0.34% together with Sr2CuO3 (kBTN/J≈0.25%) and γ-LiV2O5 (kBTN/J<0.16%). Sr2Cu(PO4)2 and Ba2Cu(PO4)2 were stable in air up to 1280 and 1150 K, respectively. 相似文献
165.
化合物库的组合技巧和组合合成 总被引:2,自引:0,他引:2
从化合物库的组合技巧和组合合成方法两个方面探讨了组合化学及其在药物开发中的应用。 相似文献
166.
Circular high-performance thin-layer chromatography (HPTLC) has been used to differentiate a series of twelve tricyclic neuroleptics, using both normal phase and reverse phase procedures. The use of normal phase systems also allows the resolution of geometric isomers of chlorprothixene, clopenthixol and flupenthixol. Thirteen sulphonamides and Trirnethoprim may also be distinguished using HPTLC. 相似文献
167.
研究了Zn2+、Cd2+、和Hg2+离子在碱式纤维素基磁性聚偕胺肟树脂(BMAO)上的吸附动力学。结果表明,吸附速度受粒内扩散所控制。测得粒内扩散系数分别是1.22×10-4、2.42×10-4和3.90×10-4cm2·s-1;Hg2+离子在树脂上的吸附行为符合Freundlich和Langmuir等温吸附方程;浓集因数随Hg2+离子浓度降低而上升,有利于从稀溶液中除去Hg2+离子。将树脂加至Zn2+、Cd2+或Hg2+离子浓度为50ppm的溶液中,离子去除率分别是96.1、99.9和99.3%。 相似文献
168.
169.
Fundueanu G Constantin M Bortolotti F Ascenzi P Cortesi R Menegatti E 《Macromolecular bioscience》2005,5(10):955-964
Despite the large number of publications and patents concerning pH/thermoresponsive polymers, few data are available concerning the preparation of thermoresponsive cross-linked microspheres from preformed polymers. Therefore, N-isopropylacrylamide-co-acrylamide-co-(2-hydroxyethyl acrylate) copolymers were obtained as a new thermoresponsive material with a lower critical solution temperature (LCST) around 36 degrees C, in phosphate buffer at pH 7.4, and with a cross-linkable OH group in their structure. The LCST value was determined both by UV spectroscopy and microcalorimetric analysis. These copolymers were solubilised in acidified aqueous solution below their LCST, dispersed in mineral oil, and transformed into stable microspheres by cross-linking with glutaraldehyde. The thermoresponsive microspheres were characterised by optical and scanning electron microscopy, degree of swelling, and water retention. The pore dimensions of the microspheres and the retention volumes of some drugs and typical compounds were evaluated at different temperatures by liquid chromatography. Indomethacin, as a model drug, was included in the microspheres by the solvent evaporation method. Finally, the influence of temperature and of temperature cycling on drug release was investigated. 相似文献
170.
The use of open-access mass spectrometry to monitor synthetic chemistry reactions, and also the integrity and purity of new chemical entities, has been a part of the medicinal chemist's tool-box for more than 5 years. Originally in our group at Wyeth Research there were two open-access methods available to the chemists, flow injection analysis (FIA) and liquid chromatography/mass spectrometry (LC/MS). The FIA method was approximately 3 min long, while the LC/MS method was approximately 20 min long (including an 8 min gradient). Within the first 2 years, the total number of open-access analyses increased by approximately 125%. It is interesting, however, that the number of LC/MS analyses increased by more than 285%. This is attributed to the fact that the chemists began using the LC/MS data to monitor reactions and also to check final product integrity and purity. In addition, the number of chemists performing parallel synthesis reactions has increased; thus, individual chemists can produce sample sets of up to 100 vials. This paper describes the implementation of new methodology, which accommodates the need for much faster run times and also the ability to acquire alternating positive and negative ion spectra within the same run. In addition, the instrument has been configured to e-mail the resulting processed data report to the submitting chemist. Several methods have been developed, including structure elucidation using in-source collision-induced dissociation (CID) and night-time analysis. The LC/MS methods for this system are described herein and are applicable to both industrial and academic synthetic chemistry optimization efforts. 相似文献