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71.
The utility of triple-quantum (TQ)-filtered (23)Na NMR spectroscopy for discriminating between intra- and extracellular Na(+)(Na(i)(+) and Na(e)(+), respectively) in a solid tumor in vivo was evaluated using TmDOTP(5-) as a (23)Na shift reagent. Infusion of 80 mM TmDOTP(5-) without added Ca(2+) produced baseline-resolved Na(i)(+) and Na(e)(+) peaks in both single-quantum (SQ) and TQ-filtered (23)Na spectra. The Na(i)(+) signal represented 22+/-4% of the SQ spectrum, but 59+/-10% of the TQ-filtered spectrum. Therefore, the Na(i)(+) contribution in TQ-filtered spectra is much higher than in SQ spectra. Both SQ and TQ-filtered Na(i)(+) signals increased by about 75% 1 h after sacrificing the animal. The TQ-filtered relaxation times did not change during this time, indicating that changes observed in TQ-filtered spectra collected with a preparation time of 3 ms represent changes in the concentration of sodium ions contributing to the TQ-filtered signal. Similar experiments were conducted without TmDOTP(5-) to determine changes in the Na(e)(+) signal in the absence of the shift reagent. The changes in total SQ and TQ-filtered signals 1 h after sacrificing the animal showed that the SQ Na(e)(+) signal decreased by approximately 35%, while the TQ-filtered Na(e)(+) signal did not change significantly. This demonstrates that the TQ-filtered (23)Na signal is relatively insensitive to changes in Na(e)(+) content. To our knowledge, this work represents the first evaluation of multiple-quantum-filtered (23)Na spectroscopy to discriminate between intra- and extracellular Na(+) in a solid tumor in vivo. 相似文献
72.
The quantum group GL
p,q(2) is known to be related to the Jordanian GLh,h(2) via a contraction procedure. It can also be realised using the generators of the Hopf algebra G
r,s. We contract the G
r,s quantum group to obtain its Jordanian analogue G
m,k, which provides a realisation of GLh,h(2) in a manner similar to the q-deformed case. 相似文献
73.
Shapiro EM Borthakur A Bansal N Leigh JS Reddy R 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2000,143(1):213-216
We describe the characterization of a (23)Na temperature-dependent chemical shift and relaxation rates in the complex, Na(4)HTm[DOTP]. This is the first characterization of a (23)Na temperature-dependent chemical shift in a nonmetallic sample. The (23)Na temperature-dependent chemical shift coefficient is approximately -0. 5 PPM/ degrees C for both an aqueous solution and a 6% agarose gel of this compound. This is 50 times the magnitude of the temperature-dependent chemical shift coefficient of water protons. The relaxation times, T(1), T(2f), and T(2s) increased by 0.1, 0.01, and 0.05 ms/ degrees C, respectively. Applications of these unique properties for designing an MRI technique for monitoring heat deposition in tissue and tissue phantoms are discussed. 相似文献
74.
Deepak S. Langhe Jong K. Keum Eric Baer 《Journal of Polymer Science.Polymer Physics》2011,49(2):159-171
A layer multiplying coextrusion process was used to produce multilayered polypropylene/polystyrene (PP/PS) films with various nucleating agents. When heated into the melt, the thin PP layers broke up into submicron PP droplets that exhibited fractionated crystallization. If the initial PP layers were 20 nm or less, the resulting droplets exhibited exclusively homogeneous nucleation. If a nucleating agent was added, the systematic departure from homogeneous nucleation provided insight into the nature of the heterogeneous nucleation. In this study, we used thermal analysis, atomic force microscopy (AFM), and wide angle X‐Ray scattering (WAXS) to examine the effect of two nucleating agents. We confirmed with WAXS and AFM that a soluble sorbitol nucleating agent for the PP α‐form operates in three concentration regimes as proposed in a previous study. Morphologically, homogeneous nucleation of the submicron droplets produced a granular texture. The correlation length from small‐angle X‐Ray scattering (SAXS) suggested that the grains contained 1–3 mesophase domains. Drawing on classical nucleation theory, the critical size nucleus of an individual mesophase domain was estimated to be about 2 nm3, which was considerably smaller than the mesophase domain. This pointed to mesophase crystallization that included the processes of nucleation and growth. Additional experiments were performed with nucleating agents for the PP β‐form. However, they were not effective in nucleating crystallization of the droplets, presumably because they were essentially insoluble in PP and the nucleating particles were too large to be accommodated in the PP droplets. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2011 相似文献
75.
A new palladium catalyzed protocol for an atom-efficient cross-coupling reaction of triarylbismuths with aryl halides and triflates has been described. The palladium catalytic system with Cs2CO3 base was found to be very efficient in DMA solvent to furnish excellent yields of cross-coupled functionalized biaryls in short reaction times. 相似文献
76.
We use lookback time versus redshift data from galaxy clusters (Capozziello et al., 2004 [9]) and passively evolving galaxies (Simon et al., 2005 [62]), and apply a Bayesian prior on the total age of the Universe based on WMAP measurements, to constrain dark energy cosmological model parameters. Current lookback time data provide interesting and moderately restrictive constraints on cosmological parameters. When used jointly with current baryon acoustic peak and Type Ia supernovae apparent magnitude versus redshift data, lookback time data tighten the constraints on parameters and favor slightly smaller values of the nonrelativistic matter energy density. 相似文献
77.
A Raman scattering study of the v3 vibration—rotation band in methyl iodide as a function of temperature and dilution (in cyclohexane) has been performed. All the data satisfy the second moment criterion. Detailed information about rotational correlation function, angular velocity correlation function, various correlation times and mean-square torque has been obtained. The correlation function, in the pure liquid, decays slowly with decrease in temperature whereas it decays faster with decreasing concentration in cyclohexane. It has been shown, from a consideration of the second moment as a function of concentration, that the contribution of collision-induced scattering to the v3 band of methyl iodide is negligible. Applicability of a simple “damped librator model”, with a view to understanding certain aspects of the rotational motion in methyl iodide, is discussed. 相似文献
78.
A monomer design having a bulky terminal tricyclodecane (TCD) unit linked via hydrogen bondable urethane to an ethyleneoxy methacrylate unit, and capable of generating three‐dimensional honeycomb patterns upon solvent casting has been investigated. Random copolymers as well as a diblock copolymer Poly(Sty42‐b‐TCD18) of this monomer with styrene were prepared by free‐radical polymerization route and atom transfer radical polymerization (ATRP) route. Morphology characterization was carried out using scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis. Particle size was measured by dynamic light scattering measurements (DLS). Irrespective of the wide differences in molecular weight and polydispersity index values, the random copolymers having TCD content >30 mol % were found to form microporous films upon solvent casting from a THF/water 9:1 solvent combination. The amount of TCD in the copolymer was found to have an influence on the pore size formed. The diblock copolymer formed microspheres ~200 nm in diameter. The thermal properties of all the polymers were studied using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), and the copolymers were found to have good thermal stability. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1278–1288, 2008 相似文献
79.
Neetu Bansal 《Transition Metal Chemistry》2009,34(6):695-702
The kinetics and mechanism of the mercury(II)-catalysed ligand substitution reaction between potassium hexacyanoferrate(II)
and 2-methylpyrazine (2-Mepz), in potassium hydrogen phthalate buffer of pH 3.50 ± 0.02 at 25.0 ± 0.1 °C and constant ionic
strength of 0.1 M, were studied spectrophotometrically by measuring the absorbance of the yellow-coloured product at 447 nm
(λmax). The reaction was studied under pseudo-first-order conditions using excess of 2-Mepz. The reaction was found to obey first-order
dependence in concentration of both [Fe(CN)6]4− and 2-Mepz. At higher concentrations of 2-Mepz, the effect of [2-Mepz] levels off. A complex behaviour is observed on varying
[Hg2+]. The effect of pH on the reaction rate was also analysed. The effects of dielectric constant and water content of the reaction
medium have been interpreted in terms of the formation of a polar activated complex and suggest an Id mechanism. The inhibitory effect of 2,3-dimercaptopropanol on the reaction was also studied and explained in terms of binding
of this species to the catalyst. 相似文献
80.
Vivekanandan Kannan Pradeep Narayanaswamy Deepak Gadamsetty Partha Hazra Anand Khedkar Harish Iyer 《Rapid communications in mass spectrometry : RCM》2009,23(7):1035-1042
Glycoforms of glargine expressed in Pichia pastoris were isolated by high‐performance liquid chromatography and analyzed by a series of chemical and mass spectrometric methods for the identification of various glycoforms, glycosylation position, nature and structure of glycans. Reduction and alkylation, peptide mapping techniques were used to decipher the amino acid site at which glycosylation had taken place. Chemical methods were coupled with mass spectrometry techniques such as electrospray ionization and matrix‐assisted laser desorption/ionization for identification of the glycosylation site. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献