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991.
Hornung Philipp Leopold-Wildburger Ulrike Mestel Roland Palan Stefan 《Central European Journal of Operations Research》2015,23(2):357-373
Central European Journal of Operations Research - We conduct laboratory experiments incorporating different market structures and insiders who compete with imperfectly informed traders. The... 相似文献
992.
993.
Four targeted octasubstituted zinc azaphthalocyanines (ZnAzaPc), substituted with thiophen-2-yl groups and ortho-substituted phenoxy groups, were obtained by cyclotetramerization of 5-aryloxy-6-(thiophen-2-yl)pyrazine-2,3-dicarbonitriles. Thiophen-2-yl substituents are known to extend the macrocyclic conjugation, and thereby cause red-shifted UV–Vis Q-bands. Peripheral phenoxy groups with bulky ortho substituents are expected to suppress aggregation and thereby improve solubility of these compounds. The reagent Zn(quinoline)2Cl2 was used for one-step syntheses of these ZnAzaPc. Four tetrasubstituted ZnAzaPc, with phenoxy, (2-isopropyloxy)phenoxy, (2-isopropyl)phenoxy or (2-tert-butyl)phenoxy substituents, were obtained as controls from 5-aryloxypyrazine-2,3-dicarbonitriles. The tetra- and octa-substituted ZnAzaPc, 5 and 6, were obtained in 30–50% yields after purification by chromatography on silica. UV–Vis Q-bands with high molar extinction coefficients (100 000–160 000), were observed at 635 nm for compounds 5, and at 660–665 nm for 6. Grass-green solutions were obtained of compounds 6 in most organic solvents, whereas the less soluble compounds 5 gave blue-green solutions. 2D NMR methods were applied in analyses of DMSO-d6 solutions of ZnAzaPc 5 and 6. Broad and partly overlapping 1H NMR signals for some of the compounds indicate some aggregation as well as presence of two or more structural isomers. Molecular ions of ZnAzaPc 5 and 6 were determined by mass spectrometry (MALDI-TOF). 相似文献
994.
Fuji T Suzuki Y Horio T Suzuki T Mitrić R Werner U Bonačić-Koutecký V 《The Journal of chemical physics》2010,133(23):234303
Ultrafast photodynamics of furan has been studied by time-resolved photoelectron imaging (TRPEI) spectroscopy with an unprecedented time resolution of 22 fs. The simulation of the time-dependent photoelectron kinetic energy distribution (PKED) has been performed with ab initio nonadiabatic dynamics "on the fly" in the frame of time-dependent density functional theory. Based on the agreement between experimental and theoretical time-dependent photoelectron signal intensity as well as on PKED, precise time scales of ultrafast internal conversion from S(2) over S(1) to the ground state S(0) of furan have been revealed for the first time. Upon initial excitation of the S(2) state which has π-π* character, a nonadiabatic transition to the S(1) state occurs within 10 fs. Subsequent dynamics invokes the excitation of the C-O stretching and C-O-C out of plane vibrations which lead to the internal conversion to the ground state after 60 fs. Thus, we demonstrate that the TRPEI combined with high level nonadiabatic dynamics calculations provide fundamental insight into ultrafast photodynamics of chemically and biologically relevant chromophores. 相似文献
995.
996.
997.
Falk Liebner Emmerich Haimer Martin Wendland Marie‐Alexandra Neouze Kerstin Schlufter Peter Miethe Thomas Heinze Antje Potthast Thomas Rosenau 《Macromolecular bioscience》2010,10(4):349-352
Bacterial cellulose produced by the gram‐negative bacterium Gluconacetobacter xylinum was found to be an excellent native starting material for preparing shaped ultra‐lightweight cellulose aerogels. The procedure comprises thorough washing and sterilization of the aquogel, quantitative solvent exchange and subsequent drying with supercritical carbon dioxide at 40 °C and 100 bar. The average density of the obtained dry cellulose aerogels is only about 8 mg · cm?3 which is comparable to the most lightweight silica aerogels and distinctly lower than all values for cellulosic aerogels obtained from plant cellulose so far. SEM, ESEM and nitrogen adsorption experiments at 77 K reveal an open‐porous network structure that consists of a comparatively high percentage of large mesopores and smaller macropores.
998.
Roland J. W. Meesters Jeroen J. A. van Kampen Mariska L. Reedijk Rachel D. Scheuer Lennard J. M. Dekker David M. Burger Nico G. Hartwig Albert D. M. E. Osterhaus Theo M. Luider Rob A. Gruters 《Analytical and bioanalytical chemistry》2010,398(1):319-328
Kaletra® (Abott Laboratories) is a co-formulated medication used in the treatment of HIV-1-infected children, and it contains the two antiretroviral protease inhibitor drugs lopinavir and ritonavir. We validated two new ultrafast and high-throughput mass spectrometric assays to be used for therapeutic drug monitoring of lopinavir and ritonavir concentrations in whole blood and in plasma from HIV-1-infected children. Whole blood was blotted onto dried blood spot (DBS) collecting cards, and plasma was collected simultaneously. DBS collecting cards were extracted by an acetonitrile/water mixture while plasma samples were deproteinized with acetone. Drug concentrations were determined by matrix-assisted laser desorption/ionization-triple quadrupole tandem mass spectrometry (MALDI-QqQ-MS/MS). The application of DBS made it possible to measure lopinavir and ritonavir in whole blood in therapeutically relevant concentrations. The MALDI-QqQ-MS/MS plasma assay was successfully cross-validated with a commonly used high-performance liquid chromatography (HPLC)–ultraviolet (UV) assay for the therapeutic drug monitoring (TDM) of HIV-1-infected patients, and it showed comparable performance characteristics. Observed DBS concentrations showed as well, a good correlation between plasma concentrations obtained by MALDI-QqQ-MS/MS and those obtained by the HPLC-UV assay. Application of DBS for TDM proved to be a good alternative to the normally used plasma screening. Moreover, collection of DBS requires small amounts of whole blood which can be easily performed especially in (very) young children where collection of large whole blood amounts is often not possible. DBS is perfectly suited for TDM of HIV-1-infected children; but nevertheless, DBS can also easily be applied for TDM of patients in areas with limited or no laboratory facilities. 相似文献
999.
Zhiyue J. Wang Roland Fischer Zili Chu Donald H. Mahoney Jr. Brigitta U. Mueller Raja Muthupillai Ellen B. James Rajesh Krishnamurthy Taylor Chung Eric Padua Elliott Vichinsky Paul Harmatz 《Magnetic resonance imaging》2010
A magnetic resonance imaging cardiac magnetic susceptometry (MRI-CS) technique for assessing cardiac tissue iron concentration based on phase mapping was developed. Normal control subjects (n=9) and thalassemia patients (n=13) receiving long-term blood transfusion therapy underwent MRI-CS and MRI measurements of the cardiac relaxation rate R2*. Using MRI-CS, subepicardium and subendocardium iron concentrations were quantified exploiting the hemosiderin/ferritin iron specific magnetic susceptibility. The average of subepicardium and subendocardium iron concentrations and R2* of the septum were found to be strongly correlated (r=0.96, P<.0001), and linear regression analysis yielded CIC (μg Fe/gwet tissue)=(6.4±0.4)·R2* septum (s−1) − (120±40). The results demonstrated that septal R2* indeed measures cardiac iron level. 相似文献
1000.
Rexford D. Newbould Stefan T. Skare Marcus T. Alley Garry E. Gold Roland Bammer 《Magnetic resonance imaging》2010
By combining a balanced steady-state free precession (bSSFP) readout with an initial inversion pulse, all three contrast parameters, T1, T2 and proton density (M0), may be rapidly calculated from the signal progression in time. However, here it is shown that this technique is quite sensitive to variation in the applied transmit RF (B1) field, leading to pronounced errors in calculated values. Two-dimensional (2D) acquisitions are taxed to accurately quantify the relaxation, as the short RF pulses required by SSFP's rapid TR contain a broad spectrum of excitation angles. A 3D excitation using a large diameter excitation coil was able to correctly quantify the parameters. While the extreme B1 sensitivity was previously problematic and has precluded use of IR-bSSFP for relaxometry, in this work these obstacles were significantly reduced, allowing the rapid quantification of T1, T2 and M0. The results may further be used to simulate image contrast from common sequences, such as a T1-weighted or fluid-attenuated inversion recovery (FLAIR) examination. 相似文献