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991.
Dr. Jens Voskuhl Dr. Christian Wendeln M. Sc. Frank Versluis M. Sc. Eva‐Corinna Fritz M. Sc. Oliver Roling M. Sc. Harshal Zope Dr. Christian Schulz Dipl.‐Phys. Stefan Rinnen Prof. Dr. Heinrich F. Arlinghaus Prof. Dr. Bart Jan Ravoo Dr. Alexander Kros 《Angewandte Chemie (International ed. in English)》2012,51(50):12616-12620
992.
Dr. Florian F. Mulks Leonie J. Bole Dr. Laia Davin Dr. Alberto Hernán-Gómez Alan Kennedy Dr. Joaquín García-Álvarez Prof. Dr. Eva Hevia 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(43):19183-19188
A straightforward alkali-metal-mediated hydroamination of styrenes using biorenewable 2-methyltetrahydrofuran as a solvent is reported. Refuting the conventional wisdom of the incompatibility of organolithium reagents with air and moisture, shown here is that the presence of moisture is key in favoring formation of the target phenethylamines over competing olefin polymerization products. The method is also compatible with sodium amides, with the latter showing excellent promise as highly efficient catalysts under inert atmosphere conditions. 相似文献
993.
Azucena Lara-Gonzalo Eva Segovia-García Alfredo Sanz-Medel 《International journal of environmental analytical chemistry》2013,93(7):856-867
The use of two modes for mass spectrometry (MS) detection with an ion trap instrument, selected ion storage (SIS) and tandem mass spectrometry (MS/MS), are compared for the solid-phase microextraction (SPME)–gas chromatography (GC) coupled to mass spectrometry (GC-MS) determination of 16 priority organochlorine pesticides (OCPs) in drinking water samples at the ultratrace levels (ng?L?1) required by official guidelines in the European legislation. Experimental parameters investigated for the SPME sample preparation were: the type of coating (100?µm polydimethylsiloxane, PDMS, and 65?µm poly(dimethylsiloxane)–divinylbenzene, PDMS/DVB), SPME modality, extraction and desorption times and desorption temperature and the methanol percentage in the SPME working solution. Under the calculated optimal conditions two methodologies were developed, one for SIS and the other for MS/MS modes. The detection limits, precision and accuracy were evaluated for both alternatives and were appropriate to the official guidelines requirements. The SPME–GC-MS(SIS) methodology offered LODs from 0.2–6.6?ng?L?1, precision below 13% and recoveries between 83 and 110%. The SPME–GC–MS/MS methodology provided limits of detection (LODs) ranging from 0.3 to 7.6 ng?L?1, % RSD were ≤14% and recoveries of 79–108% were achieved. After the results observed within an Interlaboratory Exercise, the latest MS methodology was selected for the pursued analysis in real drinking water samples. Also, the good results in this round-robin exercise validate the proposed SPME–GC–MS/MS methodology. 相似文献
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Two classical results characterizing regularity of a convergence space in terms of continuous extensions of maps on one hand, and in terms of continuity of limits for the continuous convergence on the other, are extended to convergence-approach spaces. Characterizations are obtained for two alternative extensions of regularity to convergence-approach spaces: regularity and strong regularity. The results improve upon what is known even in the convergence case. On the way, a new notion of strictness for convergence-approach spaces is introduced. 相似文献
999.
Álvarez EV Carballido-Landeira J Guiu-Souto J Taboada P Muñuzuri AP 《The Journal of chemical physics》2011,134(9):094512
The effects of volume fraction modulations on a Belousov-Zhabotinsky reaction catalyzed by the photosensitive Ru(bpy)(3)(+2) confined in an AOT microemulsion system are analyzed. Kinetic observables such as the induction time or the initial oscillation period demonstrate two different types of correlation with the volume fraction depending on whether the system is below or above the microemulsion percolation threshold. Temporal evolution also demonstrates an exponential growth of the period with the number of oscillations independent of the volume fraction of the system. 相似文献
1000.
Martinez AV DeSensi SC Dominguez L Rivera E Straub JE 《The Journal of chemical physics》2011,134(5):055107
Characterization of the molecular interactions that stabilize the folded state of proteins including hydrogen bond formation, solvation, molecular crowding, and interaction with membrane environments is a fundamental goal of theoretical biophysics. Inspired by recent experimental studies by Gai and co-workers, we have used molecular dynamics simulations to explore the structure and dynamics of the alanine-rich AKA(2) peptide in bulk solution and in a reverse micelle environment. The simulated structure of the reverse micelle shows substantial deviations from a spherical geometry. The AKA(2) peptide is observed to (1) remain in a helical conformation within a spherically constrained reverse micelle and (2) partially unfold when simulated in an unconstrained reverse micelle environment, in agreement with experiment. While aqueous solvation is found to stabilize the N- and C-termini random coil portions of the peptide, the helical core region is stabilized by significant interaction between the nonpolar surface of the helix and the aliphatic chains of the AOT surfactant. The results suggest an important role for nonpolar peptide-surfactant and peptide-lipid interactions in stabilizing helical geometries of peptides in reverse micelle environments. 相似文献