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21.
Cinchonine based phase-transfer catalysts were developed for enantioselective conjugate additions to electron deficient alkenes, including acylates, acrylonitrile, and chalcone. N-Trifulorobenzyl cinchoninium bromide 6 catalyst (20 mol %) in THF at −40 °C promoted the conjugate addition of arylketone glycolate 1 generating S-product 2 in good yields and selectivities. Catalyst, solvent, and base variations are presented along with conditions to convert the products to intermediates useful for multistep applications. 相似文献
22.
Rotationally resolved infrared spectra are reported for the X-HCN (X = Cl, Br, I) binary complexes solvated in helium nanodroplets. These results are directly compared with those obtained previously for the corresponding X-HF complexes [J. M. Merritt, J. Küpper and R. E. Miller, Phys. Chem. Chem. Phys., 2005, 7, 67]. For bromine and iodine atoms complexed with HCN, two linear structures are observed and assigned to the (2)Sigma(1/2) and (2)Pi(3/2) ground electronic states of the nitrogen and hydrogen bound geometries, respectively. Experiments for HCN + chlorine atoms give rise to only a single band which is attributed to the nitrogen bound isomer. That the hydrogen bound isomer is not stabilized is rationalized in terms of a lowering of the isomerization barrier by spin-orbit coupling. Theoretical calculations with and without spin-orbit coupling have also been performed and are compared with our experimental results. The possibility of stabilizing high-energy structures containing multiple radicals is discussed, motivated by preliminary spectroscopic evidence for the di-radical Br-HCCCN-Br complex. Spectra for the corresponding molecular halogen HCN-X(2) complexes are also presented. 相似文献
23.
24.
25.
Dawn A. Merritt J. M. Hayes 《Journal of the American Society for Mass Spectrometry》1994,5(5):387-397
Amino acids containing natural-abundance levels of 15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated by gas chromatography, combusted on-line, and the product stream sent directly to an isotope-ratio mass spectrometer. For samples of N2 gas, standard deviations of ratio measurement were better than 0.1‰ (Units for δ are parts per thousand or per million (‰).) for samples larger than 400 pmol and better than 0.5‰ for samples larger than 25 pmol (0.1‰ 15N is equivalent to 0.00004 atom % 15N). Results duplicated those of conventional, batchwise analyses to within 0.05‰. For combustion of organic compounds yielding CO2/N2 ratios between 14 and 28, in particular for N-acetyl n-propyl derivatives of amino acids, δ values were within 0.25‰ of results obtained using conventional techniques and standard deviations were better than 0.35‰. Pooled data for measurements of all amino acids produced an accuracy and precision of 0.04 and 0.23‰, respectively, when 2 mnol of each amino acid was injected on column and 20% of the stream of combustion products was delivered to the mass spectrometer. 相似文献
26.
Jose-Luis Sagripanti Avram Levy Jeannie Robertson Adam Merritt Timothy J. J. Inglis 《Photochemistry and photobiology》2009,85(4):978-986
The goal of this study was to determine the sensitivity of virulent Burkholderia pseudomallei to natural sunlight. We describe solar dosimetry calibrated to integrate radiation between 295 and 305 nm and an exposure system that minimizes thermal effects on bacterial cells. Burkholderia pseudomallei cells were either exposed to sunlight in UV transparent dishes or maintained in the dark covered by opaque foil. The cells maintained in the dark remained at constant levels for the duration of all experiments. The exposed cells nearby were killed with a kinetic studied through 5 Log10 inactivation. We found that cells in stationary phase of growth were nearly two-fold more resistant to sunlight than cells in lag or exponential growth. A virulent strain of B. pseudomallei that produced mucoid colonies showed sensitivity to sunlight similar to both a virulent strain that produced nonmucoid colonies and a strain of B. thailandensis . The inactivation of B. pseudomallei by sunlight in different types of water of environmental relevance or inside amoebae was investigated. The sensitivity of virulent B. pseudomallei was calculated and its comparison with previous studies employing monochromatic germicidal light (254 nm) is discussed . This may be the first report in the open literature of the inactivation of a virulent biological threat agent by natural sunlight. These data should assist in estimating the risk for contracting melioidosis and in predicting the time period during which B. pseudomallei remains infectious after an accidental or intentional release in the environment. 相似文献
27.
The action of cholera toxin and E. coli heat-labile enterotoxin can be inhibited by blocking their binding to the cell-surface receptor GM1. We have used anchor-based design to create 15 receptor binding inhibitors that contain the previously characterized inhibitor MNPG as a substructure. In ELISA assays, all 15 compounds exhibited increased potency relative to MNPG. Binding affinities for two compounds, each containing a morpholine ring linked to MNPG via a hydrophobic tail, were characterized by pulsed ultrafiltration (PUF) and isothermal titration calorimetry (ITC). Crystal structures for these compounds bound to toxin B pentamer revealed a conserved binding mode for the MNPG moiety, with multiple binding modes adopted by the attached morpholine derivatives. The observed binding interactions can be exploited in the design of improved toxin binding inhibitors. 相似文献
28.
C. Merritt Jr. 《应用光谱学评论》2013,48(1):263-325
Abstract The coupling of the techniques of gas chromatography and mass spectrometry has provided the chemist with one of his most powerful analytical methods. The analysis of such diverse substances as fuels, air pollutants, food flavors, smokes, protein hydrolyzates, pesticides, lipid extracts, etc. may all require the separation and identification of the components of extremely complex mixtures. 相似文献
29.
The phytoalexin resveratrol has been made using a decarbonylative Heck reaction. The acid chloride derived from 3,5-dihydroxybenzoic acid was coupled with 4-acetoxystyrene in the presence of palladium acetate and N,N-bis-(2,6-diisopropylphenyl)dihydroimidazolium chloride to give the substituted stilbene in 73% yield as the key step. 相似文献
30.
A. O. Bazarko C. G. Arroyo K. T. Bachmann T. Bolton C. Foudas B. J. King W. C. Lefmann W. C. Leung S. R. Mishra E. Oltman P. Z. Quintas S. A. Rabinowitz F. J. Sciulli W. G. Seligman M. H. Shaevitz F. S. Merritt M. J. Oreglia B. A. Schumm R. H. Bernstein F. Borcherding H. E. Fisk M. J. Lamm W. Marsh K. W. B. Merritt H. M. Schellman D. D. Yovanovitch A. Bodek H. S. Budd P. de Barbaro W. K. Sakumoto T. Kinnel P. H. Sandler W. H. Smith 《Zeitschrift fur Physik C Particles and Fields》1995,65(2):189-198
We present the first next-to-leading-order QCD analysis of neutrino charm production, using a sample of 6090
– and
-induced opposite-sign dimuon events observed in the CCFR detector at the Fermilab Tevatron. We find that the nucleon strange quark content is suppressed with respect to the non-strange sea quarks by a factor =0.477
–0.053
+0.063
, where the error includes statistical, systematic and QCD scale uncertainties. In contrast to previous leading order analyses, we find that the strange seax-dependence is similar to that of the non-strange sea, and that the measured charm quark mass,m
c
=1.70±0.19 GeV/c2, is larger and consistent with that determined in other processes. Further analysis finds that the difference inx-distributions betweenxs(x) and
is small. A measurement of the Cabibbo-Kobayashi-Maskawa matrix element |V
cd
|=0.232
–0.020
+0.018
is also presented. 相似文献