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991.
Jeon SM Jung SJ Kim HD Lim do K Lee H Kim S 《The journal of physical chemistry. B》2006,110(43):21728-21734
We have studied the adsorption and decomposition of thiophene (C4H4S) on Ge(100) using scanning tunneling microscopy (STM), high-resolution core-level photoemission spectroscopy (HRPES), and density functional theory (DFT) calculation. Analysis of S 2p core-level spectra reveals three adsorption geometries, which we assign to a Ge-S dative bonding state, a [4 + 2] cycloaddition bonding state, and a decomposed bonding state (desulfurization reaction product). Furthermore, we found that the number ratio of the three adsorption geometries depended on the molecular coverage and the annealing temperature. At low coverages, the kinetically favorable dative bonding state is initially formed at room temperature. As the molecular coverage increases, thermodynamically stable [4 + 2] cycloaddition reaction products are additionally produced. In addition, we found that as the surface temperature increased, the [4 + 2] cycloaddition reaction product either possibly desorbed as molecular thiophene or decomposed to form a metallocycle-like species (C4H4Ge2) and a sulfide (Ge2S). We systematically elucidate the changes in the bonding states of adsorbed thiophene on Ge(100) according to the thiophene coverage and annealing temperature. 相似文献
992.
Grand canonical Monte Carlo simulation is used to study the adsorption of nitrogen at 77 K and ammonia at 240 K to represent weakly polar and polar molecules, respectively, on infinite and finite graphite surfaces. These graphite surfaces were modeled with different percentages of carbons removed (defects) from the top graphite layer. Increasing the number of defects increases the adsorption and the isosteric heat of nitrogen at low pressure. At moderate pressures the amount adsorbed is less due to the disruption in the packing of the nitrogen in the first layer. In contrast, the adsorption of ammonia at all pressures is reduced as the percentage of defects is increased. This is due to the disruption in ammonia bonding caused by the defects. The condensation-like step change in the ammonia isotherm on the perfect graphite surface is not observed for any of these surfaces with defects even for the case of only 10% defects. At high percentage of defects the adsorption isotherm is close to Henry law behavior for much of the pressure range. The adsorption on finite surfaces shows that the amount adsorbed for both molecules decreases compared with that of the infinite surfaces, resulting from interaction potentials with the surface and other fluid molecules at the edge. The decrease is much greater for the ammonia adsorption because the bonding between ammonia molecules is disrupted, meaning that the adsorption cannot follow the mechanism of condensation seen for the infinite surface. 相似文献
993.
Tomislav Došlić 《Journal of mathematical chemistry》1998,24(4):359-364
Couting perfect matchings in graphs is a very difficult problem. Some recently developed decomposition techniques allowed us to estimate the lower bound of the number of perfect matchings in certain classes of graphs. By applying these techniques, it will be shown that every fullerene graph with p vertices contains at least p/2+1 perfect matchings. It is a significant improvement over a previously published estimate, which claimed at least three perfect matchings in every fullerene graph. As an interesting chemical consequence, it is noted that every bisubstituted derivative of a fullerene still permits a Kekulé structure. 相似文献
994.
微量元素硒及有机硒药物研究进展 总被引:11,自引:1,他引:11
从硒的营养学、硒的免疫学、硒的肿瘤学三个方面概括了微量元素硒的研究进展。研究表明,一些含硒有机化合物具有抗氧化性、抗炎、防癌、抗癌等药用前景。 相似文献
995.
Ján Kova Jaromír Mike Rastislav Jendelovský Martin Kello Peter Solár Peter Fedoroko 《Photochemistry and photobiology》2010,86(1):200-205
Current treatment of breast cancer is often affected by resistance to therapeutics, for which the human epidermal growth factor receptor 2 (HER2) may be responsible. Here, we report for the first time the use of hypericin-mediated photodynamic therapy (HY-PDT) in combination with a selective HER2 inhibitor (AG 825) on SKBR-3, a HER2 overexpressing human breast adenocarcinoma cell line. The results demonstrate that HY-PDT is able to degrade HER2 with an impact on its signaling cascade. Combination with AG 825 resulted in increased apoptosis induction, total degradation of HER2 and inhibition of colony formation. Downregulation of HSP90, Mcl-1, Bcl-xL and upregulation of Bax was also observed. This knowledge provides the basis for the possible application of HY-PDT in preclinical and clinical models of breast cancer treatment. 相似文献
996.
E. M. Ben’ko V. V. Lunin 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2010,84(2):215-220
Rate constants of reactions of ozone with glyoxal, glyoxylic and formic acid in aqueous solutions at pH 1.5 were determined. It was shown that iron(III) in the form of ions accelerates oxidation of glyoxal and glyoxylic acid, but does not influence reaction between ozone and formic acid. It was established that the catalyst acts effectively if its concentration is comparable to the concentration of the oxidized substrate, the optimal stoichiometric ratio (Fe3+/substrate) being close to 1/3. The catalytic reaction mechanism was studied using a competitive chelate ligand, oxalic acid. We concluded that the catalytic activity of iron(III) in the investigated reaction was due to its ability to form chelate complexes in which the substrate was more easily oxidized by molecular ozone. 相似文献
997.
Ömer Kesmez Nadir Kiraz Esin Burunkaya H. Erdem Çamurlu Meltem Asiltürk Ertuğrul Arpaç 《Journal of Sol-Gel Science and Technology》2010,56(2):167-176
SiO2 sols were prepared by hydrolysis and condensation reactions of tetraethyl orthosilicate through a one step acid or a two step acid + base catalysis process, in the presence of nitric acid and four different base catalyzers, namely trimethylamine, triethylamine, tripropylamine and tributylamine. Hydrolysis of TEOS was followed by FT-IR analyses. Particle size distributions of the sols were evaluated after predetermined durations in 1–22 days. Particle growth was seen to be faster in amine catalyzed systems than in one step acid catalyzed system. The highest rate of growth was in triethylamine catalyzed system. Glass substrates were dip coated with the prepared SiO2 sols. Effect of sol aging duration on film thickness and on light transmittance properties of the films was investigated with respect to type of base catalyst. Thicknesses of the films which were measured to be in the range of 100–400 nm, were seen to increase with aging duration of the sols. Triethylamine catalyzed system presented the highest film thickness. Films obtained from one step acid catalyzed system presented an increase of 4.8%; whereas acid + base catalyzed films provided an increase in the light transmittance of 5.7% in the first 4 days of aging. Surfaces of films were examined by FESEM and AFM. The antireflective character of the films was verified by diffuse reflectance analyses. 相似文献
998.
Waldemar Tomaszewski Vladimir M. Gun’ko Roman Leboda Jadwiga Skubiszewska-Zięba 《Central European Journal of Chemistry》2010,8(4):750-757
Solid phase extraction (SPE) of methoxy- and methylenedioxyamphetamines from diluted aqueous solutions was investigated on
carbon and polymeric adsorbents of different textures and chemical compositions. Those adsorbents were applied cartridges
packed with three chemically modified carbons prepared from plum stones (initial A2PS, oxidized A2PS-O, and reduced A2PS-H)
and commercially available adsorbents (polymeric LiChrolut EN, graphitized Hypercarb and Carboprep). Several factors influence
the recovery rates of amphetamine derivatives such as the polarity of adsorbates (free energy of salvation), the specific
surface area and surface composition of adsorbents, and the solvent characteristics. Different combinations of these factors
affect the recovery rate (R1) for high- and low-surface area adsorbents. The minimal R1 values are observed for an amphetamine
derivative at a maximal solvation effect and for a set of amphetamines adsorbed on graphitized carbons.
相似文献
999.
Erhan Temur İsmail Hakkı Boyacı Uğur Tamer Hande Unsal Nihal Aydogan 《Analytical and bioanalytical chemistry》2010,397(4):1595-1604
A very sensitive and highly specific heterogeneous immunoassay system, based on surface-enhanced Raman scattering (SERS) and
gold nanoparticles, was developed for the detection of bacteria and other pathogens. Two different types of gold nanoparticles
(citrate-stabilized gold nanosphere and hexadecyltrimethylammonium bromide (CTAB)-stabilized gold nanorod particles) were
examined and this immunoassay was applied for the detection of Escherichia coli. Raman labels were constructed by using these spherical and rod-shaped gold nanoparticles which were first coated with 5,5′-dithiobis(2-nitrobenzoic
acid) (DTNB) and subsequently with a molecular recognizer. The working curve was obtained by plotting the intensity of the
SERS signal of the symmetric NO2 stretching of DTNB at 1,333 cm−1 versus the concentration of the E. coli. The analytical performance of gold particles was evaluated via a sandwich immunoassay, and linear calibration graphs were
obtained in the E. coli concentration range of 101–105 cfu/mL with a 60-s accumulation time. The sensitivity of the Raman label fabricated with gold nanorods was more than three
times higher than spherical gold nanoparticles. The selectivity of the developed sensor was examined with Enterobacter aerogenes and Enterobacter dissolvens, which did not produce any significant response. The usefulness of the developed immunoassay to detect E. coli in real water samples was also demonstrated. 相似文献
1000.
Electropolymerization of a new phenothiazine derivative (bis-phenothiazin-3-yl methane, BPhM) on glassy carbon electrodes
leads to electroactive and conducting layers of poly-BPhM. Based on the Laviron method, the kinetic parameters (the heterogeneous
electron transfer rate constants k
s and transfer coefficients α) were calculated out of the experimental and theoretical data. The theoretical data have been
obtained by using the analogical modelling and numerical simulating method. The modified electrodes present high values of
k
s(~50s−1) in phosphate buffer solutions of different pH values. A good correlation of mathematical and numerical simulated kinetic
parameters has been obtained, with the experimental values and the norm of residuals being very close to zero. 相似文献