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101.
Becker-Szendy R Bratton CB Breault J Casper D Dye ST Ganezer K Gajewski W Goldhaber M Haines TJ Halverson PG Kielczewska D Kropp WR Learned JG LoSecco J Matsuno S McGrath G McGrew C Miller RS Price L Reines F Schultz J Sobel HW Stone JL Sulak LR Svoboda R 《Physical review D: Particles and fields》1994,49(5):2169-2173
102.
Determination of low-molecular-mass carboxylic acids in atmospheric aerosol and vehicle emission samples by capillary electrophoresis 总被引:1,自引:0,他引:1
Dabek-Zlotorzynska E Piechowski M McGrath M Lai EP 《Journal of chromatography. A》2001,910(2):331-345
A method is developed for the determination of a large number of airborne and vehicle-emitted low-molecular-mass mono- and dicarboxylic acids using capillary electrophoresis with indirect UV detection. A background electrolyte (BGE) consisting of 2,6-naphthalenedicarboxylic acid and tetradecylmethylammonium bromide, adjusted to pH 6.2 with 2,2-bis(hydroxymethyl)-2,2′,2″-nitrilotriethanol, is employed. Separations are robust using the buffered BGE, proper rinse steps, and constant current mode with migration time variations less than 3% RSD on a day-to-day basis, using different capillaries and performed by different analysts. Detection limits are at the tens of μg/l level using pressure injection. A comparison of the CE method with ion chromatography is also made. 相似文献
103.
Navamal M McGrath C Stewart J Blans P Villamena F Zweier J Fishbein JC 《The Journal of organic chemistry》2002,67(26):9406-9413
The compounds 7-methyl-6,8-bis(methyldisulfanyl)pyrrolo[1,2-a]pyrazine (5; "bis disulfide") and methanethiosulfonic acid S-((6-(methanesulfonylsulfanyl)-7-methyl)pyrrolo[1,2-a]pyrazin-8-yl) ester (6; "bis methanesulfonic acid thioester") have been synthesized to serve as alternative precursors to the major metabolite, 4, of the cancer chemopreventive oltipraz, 1, to test whether they possess similar biological activities. In the present work the mechanisms by which these compounds react with glutathione have been investigated in order to validate the assumption that they would be chemically competent in the presence of the biological thiols to give the oltipraz metabolite. A kinetic and product study was carried out in mainly aqueous media, =15% ethanol by volume, at 37 degrees C. The kinetic analysis and identification of intermediates by electrospray HPLC/MS indicate that compound 5 decomposes in two sequential reactions via thiol-disulfide interchange involving removal of the two thiomethyl groups. In contrast, 6 decomposes in three sequential steps, the first entailing formation of the diglutathionyl adduct, followed by two subsequent thiol disulfide interchange reactions involving loss of the glutathionyl moieties. Both 5 and 6, as well as oltipraz itself, give nearly quantitative yields of the metabolite 4 in reactions with glutathione. Analysis of the decay of 6 by EPR spin trapping methods indicates that less than 0.2% of the reaction flux proceeds through radicals more stable than the hydroxyl radical. 相似文献
104.
Four dendrimers (1b-4b) containing chiral vicinal diol-based subunits were prepared from their acetonide-protected precursors (1a-4a). The optical activity of these chiral dendritic structures was successfully modeled using structurally similar, low molecular weight model compounds. Using the [Phi](d) values of the low molecular weight model compounds 5b-7b, we calculated [Phi](d) values for dendrimers 1b-4b that agree to within 4.5% of the observed values. Agreement between the optical activity of the model compounds and that of the dendrimers leads to the conclusion that the conformational equilibria of the dendrimer subunits are not perturbed relative to those of the model compounds. 相似文献
105.
T. M. Moy M. Konas J. E. McGrath E. K. Fields 《Journal of polymer science. Part A, Polymer chemistry》1994,32(12):2377-2385
The dianhydride monomer 1,4-phenylenebis(phenylmaleic anhydride) was polymerized with various aromatic diamines in a one-step solution polymerization to afford high molecular weight, soluble polyimides containing backbone phenylmaleimide structures. The polymides were soluble in amide solvents, chlorinated hydrocarbons, and tetrahydrofuran at 25°C at a concentration of 15% (w/v), displayed molecular weight distributions (Mw/Mn) of 2.0–2.2 as determined by absolute GPC and showed Tg values of 240°C and above as measured by differential scanning calorimetry. In addition, polyimide thermosets were prepared from these materials by thermal cure at 350–360°C. The crosslinked polyimides displayed Tgs 20–25°C higher than their soluble precursors, and chloroform extraction indicated gel fractions ranging from 74–100% after cure. © 1994 John Wiley & Sons, Inc. 相似文献
106.
Two analogous classes of dendrimers with a single azobenzene moiety at the core have been prepared. Flexible benzyl aryl ether dendrimers 1a-e were obtained in good yields by direct alkylation of diphenolic azobenzene 3 with benzyl aryl ether dendrons [G-n]-Br (n = 0-4). In rigid dendrimers 2a-e, the azobenzene configurational switch was linked to phenylacetylene dendrons through acetylenic linkages to maintain the shape-persistent nature of these dendrimers. A comparison of these two different classes of dendrimers with azobenzene cores reveals a difference in the properties of the photochromic moiety upon dendritic incorporation as well as a significant difference in the photomodulation of dendrimer properties. The E --> Z photoisomerization quantum yield decreased markedly with increasing generation for dendrimers 1a-e but only slightly for dendrimers 2a-e. However, increasing generation did not significantly alter thermal isomerization kinetics or activation barriers. The hydrodynamic volumes of azobenzene-containing dendrimers 2b-e were significantly modulated when the azobenzene unit is subjected to irradiation, while those of dendrimers 1b-e were only slightly affected. 相似文献
107.
108.
K. M. McGrath 《Colloid and polymer science》1996,274(5):399-409
The self-assembly behaviour of the polymerisable surfactant -undecenyltrimethylammonium bromide (-UTAB) both before and after polymerisation has been investigated. In addition polymerisation of the liquid crystalline phases formed by this surfactant in aqueous solution has been studied. Introduction of the carbon-carbon double bond at the end of the hydrocarbon chain increases the rigidity of the paraffinic chains such that the Krafft curve is shifted to higher temperatures compared with that of dodecyltrimethylammonium bromide, a nonpolymerisable analogue. Both the polymerised and non-polymerised forms have been observed to have the same phase progression, with the polymer being more soluble in water such that the liquid crystalline phases formed at high surfactant concentration are accessible at room temperature. Polymerisation of the liquid crystalline phases of -UTAB indicate that polymerisation proceeds to approximately 40% (in comparison) with 80% in a non-aggregated form) and that the original monomeric matrix is undisturbed upon partial polymerisation. 相似文献
109.
Joginder Lal James E. McGrath G. S. Trick 《Journal of polymer science. Part A, Polymer chemistry》1967,5(4):795-811
The effect of polymerization temperature and solvents was determined on the crystallinity of polymers of vinyl isobutyl ether and of vinyl n-butyl ether prepared with aluminum sulfate–sulfuric acid complex catalyst. Principally, the methyl ethyl ketone (MEK)-insoluble fractions of these polymers were used for characterization. Density, per cent crystallinity by x-ray diffraction, infrared ratio, and dilatometric volume contraction of these polymer fractions were used as criteria of crystallinity. The MEK-insoluble fractions of poly(vinyl n-butyl ethers) prepared in carbon disulfide in the temperature range of ?30 to +25°C did not show any significant difference in the values of the above crystallinity parameters. The polymer obtained at 50°C. was less crystalline than the rest of the polymers. The MEK-insoluble fractions of poly(vinyl isobutyl ethers) prepared at 0–50°C. in carbon disulfide and n-heptane solvents also did not significantly differ in their degree of crystallinity. They were, however, decidedly less crystalline than the MEK-insoluble fractions of the corresponding polymers obtained at ?20°C. These data a indicate that on increasing the temperature of polymerization the crystallinity of the polymers was either unchanged or decreased slightly. The polymerizations of vinyl n-butyl ether and vinyl isobutyl ethers were also carried out in binary mixtures of carbon disulfide with n-heptane, chlorobenzene, and MEK. Generally, increasing the concentration of carbon disulfide increased the inherent viscosities of polymers as well as the weight percentage of their MEK-insoluble fractions. The MEK-insoluble fraction of poly(vinyl isobutyl ether) prepared in carbon disulfide-MEK mixture (volume ratio 2:1) was isotactic and highly crystalline. Likewise, the MEK-insoluble fractions of two polymers of vinyl n-butyl ether prepared in MEK itself were also isotactic and highly crystalline. Compared to poly(tetramethylene oxide), these latter fractions exhibited less dependence of rate of crystallization upon temperature. Consequently, at low degrees of supercooling they crystallize much more rapidly than does poly(tetramethylene oxide). 相似文献
110.
García Ruano JL Gamboa AE Gutiérrez LG Martín Castro AM Rodríguez Ramos JH Yuste F 《Organic letters》2000,2(6):733-736
A new kind of chiral dienophiles, cyclic vinyl-p-tolylsulfilimines (2a and 2b), were obtained from the corresponding (Z)-sulfinylacrylonitriles with HBF(4) and methanol. The asymmetric Diels-Alder reaction of optically pure 2a with cyclopentadiene under mild thermal or catalyzed conditions afforded only the endo-4a adduct with complete endo and pi-facial selectivities. The ability of the sulfilimine moiety to enhance the dienophilic reactivity of the double bond is similar to that of the sulfinyl group. 相似文献