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81.
The syntheses of two isoprostanyl phospholipids are described. A newly established route to 15-F(2t)-isoprostane and ent-15-epi-F(2t)-isoprostane has allowed for the selective preparation of 15-F(2t)-isoprostanyl phosphatidylethanolamine and ent-15-epi-F(2t)-isoprostanyl phosphatidylcholine. The nature of the headgroups dictates the coupling strategy used to attach the appropriately protected isoprostanes to the corresponding lysophospholipids. Preliminary 1H NMR and 31P NMR studies indicate that these isoprostanyl phospholipids aggregate in apolar solvents. 相似文献
82.
Hu W Blecking C Kralj M Šuman L Piantanida I Schrader T 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(12):3589-3597
A new class of potent DNA binding agents is presented. Dimeric calix[4]arenes with cationic groups at their upper rims and flexible alkyl bridges can be synthesized from triply acyl-protected calix[4]arene tetramines in relatively short synthetic sequences (3-5 steps). The compounds attach themselves to double-stranded nucleic acids in a noncovalent fashion, with micro- to nanomolar affinities. Guanidinium headgroups with their extended hydrogen-bonding "fingers" are more powerful than ammonium groups, and the benzylamine series is superior to the anilinium series (see below). The new ligands easily distinguish between RNA and various DNA types, and produce characteristic changes in UV/Vis, fluorescence, CD, as well as NMR spectra. Especially extended oligonucleotides of more than 100 base pairs are bound with affinities increasing from RNA (10?μM K(d))相似文献
83.
S Roters A Hepp JC Slootweg K Lammertsma W Uhl 《Chemical communications (Cambridge, England)》2012,48(77):9616-9618
Bicyclic compounds with annulated four- (AlPC(2)) and five-membered (P(2)C(3)) rings activate and capture Al-alkynides and acetonitrile at room temperature to afford bicyclic compounds with unique six-membered Al(2)PC(3) and AlNPC(3) heterocycles. 相似文献
84.
Robert Schrader 《Communications in Mathematical Physics》1985,102(1):31-46
We exhibit the analytic structure of a model of disconnected, selfintersecting random surfaces. This model is shown to have features attractive for a Monte Carlo simulation. Previously obtained numerical data show evidence that for a 3-dim embedding space the string tension vanishes above a critical temperature and has a critical exponent between 1 and 2. The glueball mass is shown to be bounded below by the mass-gap of the 3-dim Ising model.On leave of absence from Freie Universität Berlin 相似文献
85.
Jutta Langer Bernhard Schrader Volker Bastian Eberhard Jacob 《Fresenius' Journal of Analytical Chemistry》1995,352(5):489-495
Infrared spectra in the gaseous phase have been recorded for the first time for urea and the isotopomers urea-D4, urea-15N2 and urea-13C. On the base of these data a normal coordinate calculation has been performed, resulting in an optimized force field of urea, showing that, due to the very small intermolecular forces, the internal force constants increase by evaporation. This is especially true for the C=O-bond with a force constant increased by 10%.Dedicated to Professor Dr. H. Kriegsmann on the occasion of his 70th birthday, to whom since 1957 scientific contacts with the second author developed to a good friendship 相似文献
86.
We measure the point-spread function in the two main configurations of 4Pi confocal microscopy as well as in the traditional confocal arrangement and derive the optical transfer functions from the experimental data. The optical transfer functions are in good agreement with their theoretical counterparts. We find a 3.5- to 5-fold increased axial bandwidth of the 4Pi confocal microscope and hence confirm the enhanced spatial-frequency content of 4Pi images. 相似文献
87.
B. Schrader G. Baranovi S. Keller J. Sawatzki 《Fresenius' Journal of Analytical Chemistry》1994,349(1-3):4-10
The former major problem in conventional Raman spectroscopy in the visible range, the disturbing fluorescence of impurities, has now been eliminated: Raman spectra can be excited by light quanta in the near-infrared range, the energy of which is too low to excite fluorescence spectra. An inherent disadvantage of this technique, the v
4-dependence of the intensity of the Raman radiation, is compensated for by using interferometers, which are more powerful, by a factor of several hundred, than grating spectrometers. Raman spectroscopy can now be applied to analyses of real world samples bio materials, food, paintings, micro electronics and new materials, as well as to quality control of raw materials, to production and product control without special sample preparation. By using fiber bundles, Raman spectra can be recorded on line at the sample site, in containers and in real time. For successful recording of NIR FT Raman spectra of small samples a compromise between large lateral resolution and a large signal/noise ratio has to be found. Its theoretical base and practical approach is discussed. Confocal microscopes allow recording of NIR FT Raman spectra of small particles or inclusions. They can be coupled to the spectrometer by fiber optics, so that they may be placed at some distance from the spectrometer. By using computer-driven x-y stages, systematic mapping of the distribution of specific compounds on the surface of different samples is possible with the FT Raman microscope, as well as with the ordinary sample arrangement. 相似文献
88.
The gas phase reaction of alpha-pinene with the atmospheric oxidant ozone was investigated by using the capabilities of both gas chromatography-cryocondensation-Fourier transform infrared spectroscopy (GC-FT-IR) and gas chromatography-mass spectrometry (GC-MS), for the identification of the reaction products formed. The reaction was carried out in a flow reaction chamber from where the compounds were sampled on Tenax-containing adsorption cartridges. The reaction mixture was injected onto the column after thermodesorption and analyzed using both GC-IR and GC-MS. Twenty compounds could be detected, including the reactant alpha-pinene and it's impurities tricyclene and camphene. Eleven compounds were identified by spectra comparison with either reference data or spectra obtained from commercial standards. Four compounds were tentatively identified from their IR and MS spectra, while from the remaining two compounds the nature of basic functional groups could be established. 相似文献
89.
This paper reviews the fabrication of organic and metal nanoclusters in polymer matrices by three co-deposition techniques. In particular, the structure and properties of polytetrafluoroethylene (PTFE), polychlortrifluoroethylene (PCTFE), polyparaphenylene sulphide (PPS), polystyrene (PS) and polyparaxylylene (PPX) films, containing gold (Au) and dye clusters are discussed. For the first time, dye-filled polymers and multi-component films, consisting of both Au nanoparticles and dye molecules, dispersed in the PTFE matrix were studied. A low temperature plasma was used for film structure modification. Cluster formation process was studied using optical spectroscopy in situ. Transmission electron microscopy (TEM), atomic force microscopy (AFM) and ellipsometry were used for characterisation of the grown films. During Au-PTFE film growth plasmon band shifted from 460-480 nm to 560 nm. Au cluster diameter was in the 3-7 nm range. Plasma treatment of the vapours led to formation of smaller, but more aggregated clusters. During Au-PPS film deposition a two-step growth mechanism was discovered. At the beginning of film growth the plasmon band at 540 nm appeared, but as thickness increased, the band at 430 nm dominated. Without plasma treatment a disordered mixture was deposited, while with plasma treatment large Au aggregates confined with PPS matrix having plasmon band at 620 nm were formed. Dye cluster formation depends on the dye ability to aggregate, its concentration and the properties of the polymer matrix. But cluster formation can also be tuned by varying the deposition conditions. Laser beam evaporation promoted cluster formation, while plasma treatment and dilution in a polymer matrix prevented cluster formation. In all cases both equilibrium and non-equilibrium film structure can be formed using kinetic factor. Asymmetric molecules with bulky substituents were oriented in polymer matrices by applying an electric field in situ or by corona poling. These molecules did not aggregate even at high dye load. The films exhibited second harmonic generation, which demonstrated chromophore orientation in the polymer matrices. 相似文献
90.
An indirect method of arsenic determination in the submicrogram range via the determination of molybdenum is presented here. High sensitivity is achieved by combination of the chemical amplification during formation of dodecamolybdoarsenic acid (arsenic: molybdenum ratio 1 12) with multiplication due to the formation of ion-association complexes during flotation-spectrophotometric molybdenum determination with crystal violet (molar ratio 1 2). Thus, the amplification factor relating to arsenic is 24.Dodecamolybdoarsenic acid is formed in a weakly acidic medium and is quantitatively extracted byn-butanol. Back extraction of the heteropoly acid to the aqueous phase and its simultaneous destruction provides the basis for the reaction of released molybdate ions with thiocyanate ions. The molybdenum-thiocyanate complex forms a sparingly soluble ion-association complex with crystal violet which can be floated with toluene on the phase boundary (film flotation). After separation of the aqueous phase the floated molybdenum compound is dissolved in acetone and the resulting free crystal violet ions are subjected to photometric determination at 590 nm as equivalent of the concentration of arsenic. The molar absorptivity of crystal violet is 3.2 · 1051 · mol–1 · cm–1. Beer's law is obeyed in a concentration range from 0.01 to 1 g Mo · ml–1 (0.001–0.1 g As · ml–1). The resulting detection limit for arsenic is 1 ng · ml–1. 相似文献