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961.
Opilik L Bauer T Schmid T Stadler J Zenobi R 《Physical chemistry chemical physics : PCCP》2011,13(21):9978-9981
Lipid domains in supported lipid layers serve as a popular model to gain insight into the processes associated with the compartmentalization of biological membranes into so-called lipid rafts. In this paper, we present reproducible tip-enhanced Raman spectra originating from a very small number of molecules in a lipid monolayer on a gold surface, probed by the apex of a nanometer-sized silver tip. For the first time, we show large (128 × 128 pixels), high-resolution (< 50 nm) tip-enhanced Raman images of binary lipid mixtures with full spectral information at each pixel. 相似文献
962.
The purpose of the present paper is to discuss the role of second order elliptic operators of the type on the existence of a positive solution for the problem involving critical exponent where Ω is a smooth bounded domain in , , and λ is a real parameter. In particular, we show that if the function has an interior global minimum point x0 such that is comparable to , where and is the identity matrix of order n, then the range of values of λ for which the problem above has a positive solution can change drastically from to . 相似文献
963.
The surface tension of a low molar mass liquid crystal (LMMLC), 4-cyano-4'-n-heptyloxybiphenyl (70CB), was measured as a function of temperature using the pendant drop method, forming drops of different volumes ranging from 5 to 11 mm3. Contact angles formed by drops of 70CB in the nematic and isotropic phases on plates of polystyrene (PS) and of a liquid crystal polymer (LCP), VECTRA A910, were also measured. Only large drops could be used for surface tension analysis. It was shown that in the nematic phase the surface tension of 70CB decreases with increasing temperature, and that in the isotropic phase the surface tension increases with increasing temperature. Using the values of contact angle and of surface tension of 7OCB it was possible to evaluate the interfacial energy between 7OCB and PS and between 7OCB and VECTRA. The interfacial energy between 7OCB and PS, and between 7OCB and VECTRA, decreased with increasing temperature for ranges of temperatures corresponding to both phases of 70CB. 相似文献
964.
Renato Sousa Lima Paulo Augusto Gomes Carneiro Leão Alessandra Maffei Monteiro Maria Helena de Oliveira Piazzetta Angelo Luiz Gobbi Luiz Henrique Mazo Emanuel Carrilho 《Electrophoresis》2013,34(20-21):2996-3002
In this communication, we describe the fabrication and electric characterization of a hybrid glass/SU‐8 microchannels for high‐performance electrokinetic applications. The bonding process employed SU‐8 film as intermediate layer with reduced baking times; all the procedure took less than 50 min (only about 10 min disregarding the cleaning and dehydration steps). Additionally, further steps to improve the adhesion of the substrate to the SU‐8 were not needed. The developed configuration aggregates the advantages of both substrates, including (i) simple fabrication techniques; (ii) high compatibility for integration of microelectromechanical, optical, and electrochemical components (SU‐8); (iii) high and stable electroosmotic mobility (μEO); and (iv) satisfactory heat dissipation capacity (glass). Electroosmotic mobilities were measured as a function of the pH using the current monitoring method, whereas the heat dissipation capacity was investigated through Ohm's law plots for both glass and glass/SU‐8 microchips. The measured μEO values were similar for both microdevices, with mobilities of the order of 4.0–4.5 × 10?4 cm2 V?1 cm?1 at 4–12 pH range using phosphate buffer (10 and 20 mmol/L). The heat dissipation assays were carried out in microchannels filled with 20 mmol/L phosphate buffer. A considerable Joule heating was observed only at electric field strengths greater than 580 V cm?1 in hybrid glass/SU‐8 microdevices, representing a substantial increase of 48% when compared to all SU‐8 microdevices. 相似文献
965.
Christian Berchtold Vivian Müller Lukas Meier Stefan Schmid Renato Zenobi 《Journal of mass spectrometry : JMS》2013,48(5):587-593
Most pesticides, herbicides and other plant treatment agents are applied to the crop surface. Direct mass spectrometric methods, such as desorption electrospray ionization (DESI), offer new ways to analyze plant samples directly and rapidly. A strategy for the development and optimization of a DESI method for the direct determination of chemicals on complex surfaces is described. Chlorpropham (CP) was applied to potato surfaces as an example for a crop protection agent and analyzed using a self‐made DESI source. Aspects such as instrument selectivity, sensitivity and reproducibility were investigated. The MS4 fragmentation pattern of CP was analyzed to achieve the necessary detection selectivity, and is discussed in detail. Similar fragmentation was found in the ESI and DESI mass spectra, indicating that the mechanisms of ESI and DESI are closely related. A DESI method for semi‐quantification of CP on potatoes was developed. Detection limits of 6.5 µg/kg were found using MS/MS. The reproducibility, in the range of 12% (signal variation), appears to be sufficient for semi‐quantitative measurements. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
966.
967.
This work forms part of an investigation which seeks to determine metal complexes in a solid phase by photoacoustic spectrometry (PAS). Results of spectral determination of Co(II) complexes are introduced. The method is based on Co(II) colorimetric reaction with 3-(2-pyridyl)-5,6-bis(4-sulfophenyl)-1,2,4-triazine (FST, ferrozine) retained on an anion-exchange resin, DEAE Sephadex A-25. The immobilization of Co(II) on the solid phase is combined with PAS measurement. A numerical approach is applied to reduce noise in the spectral data. At λ = 477 nm, the calibration for Co(II) is linear over the range 14–300 μgL− 1. The Co(II) concentration in water samples was determined by conventional photoacoustic measurement. The relative standard deviation (R.S.D.) of the method for the calibration is < 5%. Under optimized conditions, the obtained analytical features were LOD 14 μgL− 1 and LOQ 45 μgL− 1. 相似文献
968.
Felipe A. Santos Paula M. Lima Renato C. F. Neves Paula M. Moraes Carlos A. P��rez Marcelo O. A. Silva Marco A. Z. Arruda Gustavo R. Castro Pedro de Magalh?es Padilha 《Mikrochimica acta》2011,173(1-2):43-49
An investigation was made on plasma samples obtained after protein separation. The proteome of the plasma of Nile tilapia (Oreochromis niloticus) was separated by 2D PAGE, and manganese and zinc in protein spots was qualitatively and quantitatively determined by synchrotron radiation X-ray fluorescence (SR-XRF) and graphite furnace atomic absorption spectrometry (GFAAS). Manganese and zinc are present in four and six plasma protein spots, respectively. These ions are bound to proteins with molecular weights ranging from 19 to 70?kDa and with isoelectric point (pI) ranging from 4.7 to 6.3. The concentrations of manganese and zinc bound to these proteins as determined by GFAAS following acid digestion of the spots range from 0.8 to 2.6?mg of manganese, and from 1.0 to 6.3?mg of zinc, respectively, per g of protein. Figure
2D-Page Plasma 相似文献
969.
Tôrres AR Lyra Wda S de Andrade SI Andrade RA da Silva EC Araújo MC Gaião Eda N 《Talanta》2011,84(3):601-606
This work proposes the use of digital image-based method for determination of total acidity in red wines by means of acid-base titration without using an external indicator or any pre-treatment of the sample. Digital images present the colour of the emergent radiation which is complementary to the radiation absorbed by anthocyanines present in wines. Anthocyanines change colour depending on the pH of the medium, and from the variation of colour in the images obtained during titration, the end point can be localized with accuracy and precision. RGB-based values were employed to build titration curves, and end points were localized by second derivative curves. The official method recommends potentiometric titration with a NaOH standard solution, and sample dilution until the pH reaches 8.2-8.4. In order to illustrate the feasibility of the proposed method, titrations of ten red wines were carried out. Results were compared with the reference method, and no statistically significant difference was observed between the results by applying the paired t-test at the 95% confidence level. The proposed method yielded more precise results than the official method. This is due to the trivariate nature of the measurements (RGB), associated with digital images. 相似文献
970.
Zaupa G Mora C Bonomi R Prins LJ Scrimin P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(17):4879-4889
The catalytic activity of a series of Au monolayer protected colloids (Au MPCs) containing different ratios of the catalytic unit triazacyclononane?ZnII (TACN?ZnII) and an inert triethyleneglycol (TEG) unit was measured. The catalytic self‐assembled monolayers (SAMs) are highly efficient in the transphosphorylation of 2‐hydroxy propyl 4‐nitrophenyl phosphate (HPNPP), an RNA model substrate, exhibiting maximum values for the Michaelis–Menten parameters kcat and KM of 6.7×10?3 s?1 and 3.1×10?4 M , respectively, normalized per catalytic unit. Despite the structural simplicity of the catalytic units, this renders these nanoparticles among the most active catalysts known for this substrate. Both kcat and KM parameters were determined as a function of the mole fraction of catalytic unit (x 1 ) in the SAM. Within this nanoparticle (NP) series, kcat increases up till x 1 ≈0.4, after which it remains constant and KM decreases exponentially over the range studied. A theoretical analysis demonstrated that these trends are an intrinsic property of catalytic SAMs, in which catalysis originates from the cooperative effect between two neighboring catalytic units. The multivalency of the system causes an increase of the number of potential dimeric catalytic sites composed of two catalytic units as a function of the x 1 , which causes an apparent increase in binding affinity (decrease in KM). Simultaneously, the kcat value is determined by the number of substrate molecules bound at saturation. For values of x 1 > 0.4, isolated catalytic units are no longer present and all catalytic units are involved in catalysis at saturation. Importantly, the observed trends are indicative of a random distribution of the thiols in the SAM. As indicated by the theoretical analysis, and confirmed by a control experiment, in case of clustering both kcat and KM values remain constant over the entire range of x 1 . 相似文献