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41.
It is shown that the following conjecture of Kallaher and Ostrom [2] is correct: Hering's translation plane of order 27 is the only translation plane of odd dimension over its kernel which has a collineation group isomorphic to SL(2, w) with w prime to 5 and to the characteristic, and having no affine perspectivity. 相似文献
42.
Baldomero Esquivel Jorge Cardenas Alfredo Toscano Manuel Soriano-Garcia Lydia Rodriguez-Hahn 《Tetrahedron》1985,41(16):3213-3217
From the aerial parts of Salvia fulgens Cav. (Labiatae) a new diterpenoid with a rearranged neo-clerodane skeleton was isolated. This novel compound named salvigenolide, showed a six-seven A/B ring system with a trans fussion. A probable biogenetic route is proposed. Its structure and relative stereochemistry as in , were established by spectroscopic means and X-ray diffraction analysis. 相似文献
43.
McLoughlin D Dias R Lindman B Cardenas M Nylander T Dawson K Miguel M Langevin D 《Langmuir : the ACS journal of surfaces and colloids》2005,21(5):1900-1907
DNA interacts with insoluble monolayers made of cationic amphiphiles as well as with monolayers of zwitterionic lipids in the presence of divalent ions. Binding to dioctadecyldimethylammonium bromide (DODAB) or distearoyl-sn-glycero-3-phosphocholine (DSPC) monolayers in the presence of calcium is accompanied by monolayer expansion. For the positively charged DODAB monolayer, this causes a decrease of surface potential, while an increase is observed for the DSPC monolayers. Binding to dipalmitoyl-sn-glycero-3-phosphocholine preserves most of the liquid expanded-liquid condensed coexistence region. The liquid condensed domains adopt an elongated morphology in the presence of DNA, especially in the presence of calcium. The interaction of DNA with phospholipid monolayers is ion specific: the presence of calcium leads to a stronger interaction than magnesium and barium. These results were confirmed by bulk complexation studies. 相似文献
44.
Alexander Grigor’yan Rolando Jimenez Yuri Muranov 《Czechoslovak Mathematical Journal》2018,68(1):35-65
We introduce the notion of fundamental groupoid of a digraph and prove its basic properties. In particular, we obtain a product theorem and an analogue of the Van Kampen theorem. Considering the category of (undirected) graphs as the full subcategory of digraphs, we transfer the results to the category of graphs. As a corollary we obtain the corresponding results for the fundamental groups of digraphs and graphs. We give an application to graph coloring. 相似文献
45.
Simone Cecchini Rolando Magnanini 《Calculus of Variations and Partial Differential Equations》2010,39(1-2):121-138
We study the minimizer u of a convex functional in the plane which is not Gâteaux-differentiable. Namely, we show that the set of critical points of any C 1-smooth minimizer can not have isolated points. Also, by means of some appropriate approximating scheme and viscosity solutions, we determine an Euler–Lagrange equation that u must satisfy. By applying the same approximating scheme, we can pair u with a function v which may be regarded as the stream function of u in a suitable generalized sense. 相似文献
46.
Colón L Crespo-Hernández CE Oyola R García C Arce R 《The journal of physical chemistry. B》2006,110(31):15589-15596
The role of base sequence and conformation on the photochemistry and photophysics of thymidylyl (3'-5')-2'-deoxyadenosine sodium salt (TpdA) and 2-deoxyadenylyl (3'-5')-thymidine ammonium salt (dApT) was studied. To this end, nanosecond transient absorption at 266 nm, steady-state irradiation at 254 nm, and quantum chemical calculations were used. The transient absorption spectra show the solvated electron broad band in the visible region for each dinucleotide. In addition, low-intensity absorption bands are observed in the UV region, which are attributed to the deprotonated and protonated neutral radicals of adenine and thymine bases. Photoionization (PI) occurs by one- and two-photon pathways; the latter accounting for approximately 70% of the net PI yield. A diffusion-limited rate constant of 2.0 x 10(10) M(-1) s(-1) was obtained for the reaction of the neutral molecule with the photoejected electron in both sequences. The photodestruction yield, measured from the chromophore loss at 260 nm, decreases in the presence of well-known electron scavengers. This suggests the participation of base radical anions as one of the photodegradation pathways, which is higher in TpdA than in dApT. The intermediacy of a radical ion pair (charge separated state) between the adjacent adenine and thymine bases is proposed in the formation of the [2 + 2] cycloadduct intermediate. The [2 + 2] cycloadduct intermediate is known to be the precursor of the thymine-adenine eight-member ring photoproduct (TA*). Conformational constrains in the radical ion pair are suggested to explain the absence of the TA* photoproduct in dApT. This hypothesis is supported by semiempirical calculations performed on all relevant reactive intermediates proposed to participate in the mechanism of formation of TA*. Altogether, the results show that sequence and conformation profoundly influence the photochemistry and the photophysics of these DNA model systems. 相似文献
47.
The cycloaddition reactions of 9-substituted anthracenes and levoglucosenone were investigated under microwave irradiation and conventional heating conditions. Considering time, yields, and regioselectivity, microwave technology has proven to be an ideal tool to achieve this chemical transformation. [reaction: see text]. 相似文献
48.
Rolando Roque-Malherbe F. Diaz-Castro 《Journal of molecular catalysis. A, Chemical》2008,280(1-2):194-202
49.
Anna Szabó Rolando Pasquariello Pedro F. Costa Radmila Pavlovic Indi Geurs Koen Dewettinck Chris Vervaet Tiziana A. L. Brevini Fulvio Gandolfi Sandra Van Vlierberghe 《Macromolecular bioscience》2023,23(10):2300016
To provide prominent accessibility of fishmeal to the European population, the currently available, time- and cost-extensive feeding trials, which evaluate fish feed, should be replaced. The current paper reports on the development of a novel 3D culture platform, mimicking the microenvironment of the intestinal mucosa in vitro. The key requirements of the model include sufficient permeability for nutrients and medium-size marker molecules (equilibrium within 24 h), suitable mechanical properties (G' < 10 kPa), and close morphological similarity to the intestinal architecture. To enable processability with light-based 3D printing, a gelatin-methacryloyl-aminoethyl-methacrylate-based biomaterial ink is developed and combined with Tween 20 as porogen to ensure sufficient permeability. To assess the permeability properties of the hydrogels, a static diffusion setup is utilized, indicating that the hydrogel constructs are permeable for a medium size marker molecule (FITC-dextran 4 kg mol−1). Moreover, the mechanical evaluation through rheology evidence a physiologically relevant scaffold stiffness (G' = 4.83 ± 0.78 kPa). Digital light processing-based 3D printing of porogen-containing hydrogels results in the creation of constructs exhibiting a physiologically relevant microarchitecture as evidenced through cryo-scanning electron microscopy. Finally, the combination of the scaffolds with a novel rainbow trout (Oncorhynchus mykiss) intestinal epithelial cell line (RTdi-MI) evidence scaffold biocompatibility. 相似文献
50.
Dr. Alison C. McQuilken Quang Minh Dao Dr. Allan Jay P. Cardenas Dr. Jeffery A. Bertke Prof. Dr. Stefan Grimme Prof. Dr. Timothy H. Warren 《Angewandte Chemie (International ed. in English)》2016,55(46):14335-14339
We report a new class of frustrated Lewis pairs (FLPs) by the hydroboration of bulky isocyanates iPr2ArNCO (iPr2Ar=2,6‐iPr2C6H3) and Ph2tBuArNCO (Ph2tBuAr=2,6‐Ph2‐4‐tBuC6H2) with Piers’ borane (HB(C6F5)2). While hydroboration of smaller isocyanates such as iPr2ArNCO leads to isocyanate—N/B FLP adducts, hydroboration of the bulkier Ph2tBuArNCO allows isolation of the substrate‐free aminoborane with a short, covalent N?B bond. This confused FLP reversibly binds unsaturated substrates such as isocyanates and isocyanides, suggesting the intermediacy of a “normal” FLP along the reaction pathway, supported by high‐level DFT studies and variable‐temperature NMR spectroscopy. These results underscore the possibility of FLP behavior in systems that possess no obvious frustrated Lewis acid–base interaction. 相似文献