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161.
Let F be a graph of order at most k. We prove that for any integer g there is a graph G of girth at least g and of maximum degree at most 5k13 such that G admits a surjective homomorphism c to F, and moreover, for any F-pointed graph H with at most k vertices, and for any homomorphism h from G to H there is a unique homomorphism f from F to H such that h=fc. As a consequence, we prove that if H is a projective graph of order k, then for any finite family of prescribed mappings from a set X to V(H) (with ||=t), there is a graph G of arbitrary large girth and of maximum degree at most 5k26mt (where m=|X|) such that and up to an automorphism of H, there are exactly t homomorphisms from G to H, each of which is an extension of an f.Supported in part by the National Science Council under grant NSC89-2115-M-110-012Final version received: June 9, 2003 相似文献
162.
Gholam‐Reza Nejabat Mehdi Nekoomanesh Hassan Arabi Hamid Salehi‐Mobarakeh Gholam‐Hossein Zohuri Mojtaba Omidvar Stephen A. Miller 《Journal of polymer science. Part A, Polymer chemistry》2013,51(3):724-731
Various elastomeric polypropylenes (PPs) are synthesized through homogeneous propylene polymerization with metallocene catalyst (2‐PhInd)2ZrCl2 in the presence of different cocatalyst mixtures: triethylaluminum (TEA)/methylaluminoxane (MAO) or triisobutylaluminum (TIBA)/MAO in the range of AlAlR3/AlMAO = 0.0–0.9. The cocatalyst formulation impacts the resultant polymer microstructure and the thermal and dynamic mechanical properties of the produced PPs. 13C NMR analysis of the polymers reveals essentially atactic PP, with mmmm = 7.9%, when AlAlR3/AlMAO = 0.0. The mmmm pentad content is maximized when AlAlR3/AlMAO = 0.8; for TIBA, mmmm = 23.5%; and for TEA, mmmm = 17.6%. Differential scanning calorimetry analysis and dynamic mechanical thermal analysis corroborate these findings. Specifically, Tm, ΔHm, and Tg are essentially maximized under these conditions, and the minimum damping is observed for AlAlR3/AlMAO = 0.6–0.8. 1H NMR analysis of the mixtures of catalyst and cocatalysts (without monomer) shows very minor differences for [Zr]:AlAlR3 in the range of 1:1–1:5. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
163.
Kazem Jeddi Nader Taheri Qazvini Seyed Hassan Jafari Hossein Ali Khonakdar Javad Seyfi Uta Reuter 《Journal of Polymer Science.Polymer Physics》2011,49(4):318-326
Polymer–silicate nanocomposites based on poly (ethylene oxide), PEO, poly(methyl methacrylate), PMMA, and sodium montmorillonite clay were fabricated and characterized to investigate the effect of nanolayered silicates on segmental dynamics of PEO/PMMA blends. X‐ray results indicate the formation of an exfoliated morphology in the nanocomposites. At low silicate contents, an enhancement in segmental dynamics of blend nanocomposites and also PEO, minor component in blend, is observed at temperature region below blend glass transition. This result can be attributed to the improvement of the confinement effect of rigid PMMA matrix on the PEO chains by introducing a low amount of layered silicates. On the other hand, at high silicate contents, an enhancement in segmental dynamics of blend nanocomposites and PEO is observed at temperature region above blend glass transition. This behavior could be interpreted based on the reduction of monomeric friction between two polymer components, which can facilitate segmental motions of blend components in nanocomposite systems. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2011 相似文献
164.
Abdolreza Rezaeifard Maasoumeh Jafarpour Hossein KavousiMahboubeh Alipour Helen Stoeckli-Evans 《Polyhedron》2011,30(13):2303-2309
Benzyltributylammonium periodate (BzBu3NIO4) was prepared easily in high yield in neat water. The compound crystallized with two cations and two anions per asymmetric unit and a space group of Pna21 was determined by single-crystal X-ray diffraction. It was used practically in the clean and selective epoxidation of olefins and oxygenation of saturated hydrocarbons catalyzed by manganese (III) porphyrins in water/ethanol as a green media. The catalyst could be reused without noticeable loss of activity, and the oxidant’s by-product (BzBu3NIO3) could also be reused. The efficiency of the oxidation system depends critically upon the steric hindrances and electronic structures of both the nitrogen donors and Mn-catalysts. Some evidences suggest the involvement of a high valent Mn-oxo species as well as a six-coordinate [(L)(Por)Mn-OIO3] complex in the oxidation reactions. 相似文献
165.
BAKHERAD Mohammad BAHRAMIAN Bahram NASR-ISFAHANI Hossein KEIVANLOO Ali SANG Golnaz 《中国化学》2009,27(2):353-358
The polymer-supported palladium(II) ethylenediamine complex was used as a catalyst for the heterocyclization during Sonogashira reaction between a substituted phenyl iodide and 2-amino-3-(2-propynyl)-1,3-benzothiazolium bromide, which could readily be recovered from the reaction medium by a simple filtration, and reused without a significant loss in its activity. 相似文献
166.
Hossein Heli S. Majdi A. Jabbari N. Sattarahmady A. A. Moosavi-Movahedi 《Journal of Solid State Electrochemistry》2010,14(8):1515-1523
The electrooxidation of dextromethorphan on a composite constructed with carbon nanotube–ionic liquid–carbon microparticles was investigated by cyclic voltammetry in a 100 mM phosphate buffer solution, pH 7.40. In the voltammograms, an irreversible diffusion-controlled anodic peak appeared. The diffusion coefficient of dextromethorphan, the electron-transfer coefficient, and the standard rate constant of the electrooxidation process were found to be 3.45?×?10?6 cm2 s?1, 0.65, and 1.67?×?10?3 cm s?1, respectively. A sensitive and timesaving determination procedure was developed for the analysis of dextromethorphan, and the corresponding analytical parameters were reported. Using this method, dextromethorphan was determined with an LOD and LOQ of 8.81 and 29.36 μM in a linear range of 2.5?×?10?4 to 3.3?×?10?3 M, respectively. The proposed amperometric method was successfully applied to the analysis of commercial pharmaceutical products (syrup and oral drop), and the results were in good agreement with the declared values. 相似文献
167.
168.
Dr. Guanzhao Wu Yangxue Liu Hossein Rouh Liulei Ma Yao Tang Sai Zhang Peng Zhou Jia-Ying Wang Shengzhou Jin Dr. Daniel Unruh Dr. Kazimierz Surowiec Prof. Dr. Yanzhang Ma Prof. Dr. Guigen Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(30):8013-8020
The first asymmetric catalytic approach to multilayer 3D chirality has been achieved by using Suzuki-Miyaura cross-couplings. New chiral catalysts were designed and screened under various catalytic systems that proved chiral amide-phosphines to be more efficient ligands than other candidates. The multilayer 3D framework was unambiguously determined by X-ray structural analysis showing a parallel pattern of three layers consisting of top, middle and bottom aromatic rings. The X-ray structure of a catalyst complex, dichloride complex of Pd-phosphine amide, was obtained revealing an interesting asymmetric environment nearby the Pd metal center. Three rings of multilayer 3D products can be readily changed by varying aromatic ring-anchored starting materials. The resulting multilayer products displayed strong luminescence under UV irradiation and strong aggregation-induced emission (AIE). In the future, this work would benefit not only the field of asymmetric synthesis but also materials science, in particular polarized organic electronics, optoelectronics and photovoltaics. 相似文献
169.
170.
<正>Certain phenols and naphthols were nitrated regioselectively with Zn(NO_3)_2·6H_2O/TCT in acetonitrile as solvent at room temperature and short reaction time in good yields.The reaction condition was mild.TCT is a cheap and commercially available reagent.It performed as an acid catalyst in this transformation. 相似文献