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241.
We present the development of a microfluidically cryo-cooled planar coil for magnetic resonance (MR) microscopy. Cryogenically cooling radiofrequency (RF) coils for magnetic resonance imaging (MRI) can improve the signal to noise ratio (SNR) of the experiment. Conventional cryostats typically use a vacuum gap to keep samples to be imaged, especially biological samples, at or near room temperature during cryo-cooling. This limits how close a cryo-cooled coil can be placed to the sample. At the same time, a small coil-to-sample distance significantly improves the MR imaging capability due to the limited imaging depth of planar MR microcoils. These two conflicting requirements pose challenges to the use of cryo-cooling in MR microcoils. The use of a microfluidic based cryostat for localized cryo-cooling of MR microcoils is a step towards eliminating these constraints. The system presented here consists of planar receive-only coils with integrated cryo-cooling microfluidic channels underneath, and an imaging surface on top of the planar coils separated by a thin nitrogen gas gap. Polymer microfluidic channel structures fabricated through soft lithography processes were used to flow liquid nitrogen under the coils in order to cryo-cool the planar coils to liquid nitrogen temperature (-196 °C). Two unique features of the cryo-cooling system minimize the distance between the coil and the sample: (1) the small dimension of the polymer microfluidic channel enables localized cooling of the planar coils, while minimizing thermal effects on the nearby imaging surface. (2) The imaging surface is separated from the cryo-cooled planar coil by a thin gap through which nitrogen gas flows to thermally insulate the imaging surface, keeping it above 0 °C and preventing potential damage to biological samples. The localized cooling effect was validated by simulations, bench testing, and MR imaging experiments. Using this cryo-cooled planar coil system inside a 4.7 Tesla MR system resulted in an average image SNR enhancement of 1.47 ± 0.11 times relative to similar room-temperature coils. 相似文献
242.
P(1),P(2)-Diimidazolyl derivatives of pyrophosphate and halomethylene-bis-phosphonates have been synthesized and characterized, and the mechanism of their formation was studied. These reagents enable synthesis of dinucleoside tetraphosphates and tetraphosphonates conveniently and in high yields. 相似文献
243.
Miller SA Hiatt LA Keil RG Wright DW Cliffel DE 《Analytical and bioanalytical chemistry》2011,399(3):1021-1029
Immunoassays are important tools for the rapid detection and identification of pathogens, both clinically and in the research
laboratory. An immunoassay with the potential for the detection of influenza was developed and tested using hemagglutinin
(HA), a commonly studied glycoprotein found on the surface of influenza virions. Gold nanoparticles were synthesized, which
present multiple peptide epitopes, including the HA epitope, in order to increase the gravimetric response achieved with the
use of a QCM immunosensor for influenza. Specifically, epitopes associated with HA and FLAG peptides were affixed to gold
nanoparticles by a six-mer PEG spacer between the epitope and the terminal cysteine. The PEG spacer was shown to enhance the
probability for interaction with antibodies by increasing the distance the epitope extends from the gold surface. These nanoparticles
were characterized using thermogravimetric analysis, transmission electron microscopy, matrix-assisted laser desorption/ionization-time
of flight, and 1H nuclear magnetic resonance analysis. Anti-FLAG and anti-HA antibodies were adhered to the surface of a QCM, and the response
of each antibody upon exposure to HA, FLAG, and dual functionalized nanoparticles was compared with binding of Au–tiopronin
nanoparticles and H5 HA proteins from influenza virus (H5N1). Results demonstrate that the immunoassay was capable of differentiating
between nanoparticles presenting orthogonal epitopes in real-time with minimal nonspecific binding. The detection of H5 HA
protein demonstrates the logical extension of using these nanoparticle mimics as a safe positive control in the detection
of influenza, making this a vital step in improving influenza detection methodology. 相似文献
244.
McCarron P Emteborg H Giddings SD Wright E Quilliam MA 《Analytical and bioanalytical chemistry》2011,400(3):847-858
A candidate certified reference material (CRM) for multiple shellfish toxins (domoic acid, okadaic acid and dinophysistoxins,
pectenotoxins, yessotoxin, azaspiracids and spirolides) has been prepared as a freeze-dried powder from mussel tissues (Mytilus edulis). Along with the certified values, the most important characteristics for a reference material to be fit-for-purpose are
homogeneity and stability. Acceptable between-bottle homogeneity was found for this CRM. Within-bottle homogeneity was assessed
using domoic acid, and it was shown that repeated subsampling of the CRM can be performed precisely down to 0.35 g. Both short-
and long-term stability studies carried out under isochronous conditions demonstrated excellent stability of the various toxins
present in the material. While degradation of some analytes was observed at +60°C in short-term studies, it was determined
that shipping at ambient temperature is adequate. No instability was detected in long-term stability studies, and it was shown
that the material can be held at +18°C safely for up to 1 year. To guarantee stability of the CRM over its lifetime the stock
will be maintained at −20°C. The results of the homogeneity and stability testing show that CRM–FDMT1 is appropriate for its
intended use in quality assurance and quality control of shellfish toxin analysis methods. 相似文献
245.
Strotman NA Baxter CA Brands KM Cleator E Krska SW Reamer RA Wallace DJ Wright TJ 《Journal of the American Chemical Society》2011,133(21):8362-8371
The first example of an intramolecular asymmetric reductive amination of a dialkyl ketone with an aliphatic amine has been developed for the synthesis of Suvorexant (MK-4305), a potent dual Orexin antagonist under development for the treatment of sleep disorders. This challenging transformation is mediated by a novel Ru-based transfer hydrogenation catalyst that provides the desired diazepane ring in 97% yield and 94.5% ee. Mechanistic studies have revealed that CO(2), produced as a necessary byproduct of this transfer hydrogenation reaction, has pronounced effects on the efficiency of the Ru catalyst, the form of the amine product, and the kinetics of the transformation. A simple kinetic model explains how product inhibition by CO(2) leads to overall first-order kinetics, but yields an apparent zero-order dependence on initial substrate concentration. The deleterious effects of CO(2) on reaction rates and product isolation can be overcome by purging CO(2) from the system. Moreover, the rate of ketone hydrogenation can be greatly accelerated by purging of CO(2) or trapping with nucleophilic secondary amines. 相似文献
246.
N-[1-Alkylpyridin-4(1H)-ylidene]amides (PYAs) are a new class of easily prepared, neutral N-donor ligands that share some features in common with N-heterocyclic carbenes. They are strongly electron-donating toward metal centers, and a palladium(II) complex of one of these ligands has been shown to successfully catalyze both the Heck-Mizoroki and Suzuki-Miyaura cross-coupling reactions. 相似文献
247.
Reinemann DN Wright AM Wolfe JD Tschumper GS Hammer NI 《The journal of physical chemistry. A》2011,115(24):6426-6431
N-methyliminodiacetic acid (MIDA)-protected boronate esters are a new class of reagents that offer great promise in iterative Suzuki-Miyaura cross-coupling reactions. Compared to earlier reagents, MIDA esters are easily handled and are benchtop stable under air indefinitely. The success of this new species is tied to its unique molecular architecture. Compared to the simpler B-N containing molecules ammonia borane and trimethylamine borane, MIDA esters are much larger, and the sp(3) hybridized boron atom is secured by two five membered rings, making this molecular class stable for spectroscopic study. Here, we present infrared, Raman, and surface enhanced Raman (SERS) spectra of methylboronic acid MIDA ester. Comparisons of the spectroscopic results to those from electronic structure calculations suggest that the B-N stretching mode in this molecule lies in the range 560-650 cm(-1), making it among the lowest energy vibrations observed to date that can be primarily attributed to B-N stretching. 相似文献
248.
Less RJ Wilson TC McPartlin M Wood PT Wright DS 《Chemical communications (Cambridge, England)》2011,47(36):10007-10009
The ready formation of a range of transition metal complexes of the pentacyanocyclopentadienide anion via ligand transfer reactions employing Na[C(5)(CN)(5)] indicates that the [C(5)(CN)(5)](-) anion has an extensive transition metal coordination chemistry and is not such a weakly coordinating anion. 相似文献
249.
García F Less RJ McPartlin M Michalski A Mulvey RE Naseri V Stead ML Morán de Vega A Wright DS 《Chemical communications (Cambridge, England)》2011,47(6):1821-1823
The structures of a series of spherical host-guest complexes [{MeE(PPh)(3)Li(4)·3thf}(4)(μ(4)-X)](-) (E = Al, [1X](-); E = Ga, [2X](-); E = In, [3X](-)) reveal that changing the halide ions (X = Cl, Br, or I) within their central tetrahedral Li(4) sites has negligible effect on the structural parameters. 相似文献
250.