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991.
James W. Favell Kerry L. Wilkinson Ieva Zigg Sarah M. Lyons Renata Ristic Carolyn J. Puglisi Eric Wilkes Randell Taylor Duane Kelly Greg Howell Marianne McKay Lucky Mokwena Tim Plozza Pei Zhang AnhDuyen Bui Ian Porter Orrin Frederick Jasha Karasek Colleen Szeto Bruce S. Pan Steve Tallman Beth Anne McClure Hui Feng Eric Herv Anita Oberholster Wesley F. Zandberg Matthew Noestheden 《Molecules (Basel, Switzerland)》2022,27(15)
Vineyard exposure to wildfire smoke can taint grapes and wine. To understand the impact of this taint, it is imperative that the analytical methods used are accurate and precise. This study compared the variance across nine commercial and research laboratories following quantitative analysis of the same set of smoke-tainted wines. In parallel, correlations between the interlaboratory consensus values for smoke-taint markers and sensory analyses of the same smoke-tainted wines were evaluated. For free guaiacol, the mean accuracy was 94 ± 11% in model wine, while the free cresols and 4-methylguaiacol showed a negative bias and/or decreased precision relative to guaiacol. Similar trends were observed in smoke-tainted wines, with the cresols and glycosidically bound markers demonstrating high variance. Collectively, the interlaboratory results show that data from a single laboratory can be used quantitatively to understand smoke-taint. Results from different laboratories, however, should not be directly compared due to the high variance between study participants. Correlations between consensus compositional data and sensory evaluations suggest the risk of perceivable smoke-taint can be predicted from free cresol concentrations, overcoming limitations associated with the occurrence of some volatile phenols, guaiacol in particular, as natural constituents of some grape cultivars and of the oak used for barrel maturation. 相似文献
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Georgina E. Lang Sarah L. Waters Dominic Vella Alain Goriely 《Journal of Elasticity》2017,129(1-2):239-256
Diffuse brain injury is caused by rapid rotation of the head, and causes strain injury to tissue throughout the brain. Following strain injury, axons exhibit delayed recovery, showing regional buckling behavior immediately after stretch and returning to their original appearance over an extended period of time. This axonal buckling is hypothesized to occur as a result of localized stretching within the axon: Rapid strain causes mechanical damage to microtubules, increasing the effective length of axons. This damage is repaired gradually returning the axon to its initial length.Here, we test the hypothesis that localized stretching is a possible explanation for the regional buckling behavior. An elongated region of axon is modeled as an Euler beam on an elastic foundation, where the foundation represents the surrounding brain tissue, which consists of glial cells and extracellular matrix. After stretch the elastic foundation returns immediately to its pre-stretch length, while the axon is initially elongated and returns to its original length over a longer period of time. The model exhibits solutions similar to those observed experimentally in post-stretch axons, with undulations that have a similar wavelength and amplitude. 相似文献
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Larisa Karpenko-Jereb Edyta Rynkowska Wojciech Kujawski Sarah Lunghammer Joanna Kujawa Stéphane Marais Kateryna Fatyeyeva Corinne Chappey Anne-Marie Kelterer 《Ionics》2016,22(3):357-367
The work is devoted to a computational study of three types of cationic polymeric membranes in Li+-ionic form, in water and methanol environments, at various solvation levels. The studied membranes Nafion, IonClad, and M3 possess the perfluorinated backbone; however, various side chains were terminated with the functional groups of distinctly different ionic strength. The paper discusses the structural features of the membrane-solvent clusters as well as an influence of the side chain nature on the dissociation of the functional groups and the binding energy of the solvent molecules. Additionally, the paper compares the obtained results for Li+-Nafion membrane in water with the results published earlier for H+ and Na+ forms. 相似文献
996.
A novel preparation path for the synthesis of MnO2-based wire-shaped catalyst material for lithium-air electrodes is presented. The electrode was prepared with direct laser-transfer, which is solvent free and considered environmental benign. High specific charge, 869 and 2978 A h kg?1, was achieved for the total mass of one electrode and carbon content, respectively. The electrode faded about 11% of the initial specific charge after 60 cycles. 相似文献
997.
Palladium‐Catalyzed Chemoselective and Biocompatible Functionalization of Cysteine‐Containing Molecules at Room Temperature
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Riyadh Ahmed Atto Al‐Shuaeeb Dr. Sergii Kolodych Dr. Oleksandr Koniev Dr. Sébastien Delacroix Stéphane Erb Stéphanie Nicolaÿ Dr. Jean‐Christophe Cintrat Prof. Jean‐Daniel Brion Dr. Sarah Cianférani Dr. Mouâd Alami Dr. Alain Wagner Dr. Samir Messaoudi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(32):11365-11370
The third generation of aminobiphenyl palladacycle pre‐catalyst “G3‐Xantphos” enables functionalization of peptides containing cysteine in high yields. The conjugation (bioconjugation) occurs chemoselectively at room temperature under biocompatible conditions. Extension of the method to protein functionalization allows selective bioconjugation of the trastuzumab antibody. 相似文献
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A dispersive liquid–liquid micellar microextraction for the determination of pharmaceutical compounds in wastewaters using ultra‐high‐performace liquid chromatography with DAD detection
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Sarah Montesdeoca‐Esponda Cristina Mahugo‐Santana Zoraida Sosa‐Ferrera José Juan Santana‐Rodríguez 《Biomedical chromatography : BMC》2015,29(3):353-356
A dispersive liquid–liquid micellar microextraction (DLLMME) method coupled with ultra‐high‐performance liquid chromatography (UHPLC) using Diode Array Detector (DAD) detector was developed for the analysis of five pharmaceutical compounds of different nature in wastewaters. A micellar solution of a surfactant, polidocanol, as extraction solvent (100 μL) and chloroform as dispersive solvent (200 μL) were used to extract and preconcentrate the target analytes. Samples were heated above critical temperature and the cloudy solution was centrifuged. After removing the chloroform, the reduced volume of surfactant was then injected in the UHPLC system. In order to obtain high extraction efficiency, the parameters affecting the liquid‐phase microextraction, such as time and temperature extraction, ionic strength and surfactant and organic solvent volume, were optimized using an experimental design. Under the optimized conditions, this procedure allows enrichment factors of up to 47‐fold. The detection limit of the method ranged from 0.1 to 2.0 µg/L for the different pharmaceuticals. Relative standard deviations were <26% for all compounds. The procedure was applied to samples from final effluent collected from wastewater treatment plants in Las Palmas de Gran Canaria (Spain), and two compounds were measured at 67 and 113 µg/L in one of them. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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