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1.
TheN-(2-phenylethyl)amide of-(1, 1-ethylenedioxy)-ethyl--hydroxybutyric acid (II) and theN-(p-methoxybenzyl)amide of-(1, 1-ethylenedioxy)-ethyl--hydroxybutyric acid (III) have been synthesized and the crystal structure ofIII has been solved. CompoundIII, C16H23O5N, crystallizes in the monoclinic space groupP21/c witha=12.572(2),b=11.149(2),c=12.317(2) Å and=106.53(1)°. The structure was solved by direct methods, and refined by full-matrix least squares to giveR=0.040 (R
w
=0.047) for 2004 intensities. The dioxolane ring has a deformed half-chair conformation. 相似文献
2.
We investigate the relaxation phenomena in a polymer (polystyrene)/liquid crystal (4-cyano-4'-n-octyl-biphenyl) system, in its homogeneous isotropic phase near the isotropic-isotropic, isotropic-nematic, and isotropic-smectic coexistence curve, using both polarized and depolarized photon correlation spectroscopy (PCS). We study this system for different polystyrene molecular weights (4750, 12 500, and 65 000 g/mol), different compositions (50, 40, 30, and 10% polystyrene (PS) by weight), and different temperatures close to phase boundaries. First of all, we determine the phase diagrams of this system for the different molecular weights. The shape of the phase diagrams strongly depends on the molecular weight. However, in all cases, at low temperatures, these systems separate into an almost pure liquid crystalline (LC) phase and polystyrene-rich phase. PCS measurements show that the relaxation processes in the homogeneous phase are not affected by the proximity of the nematic, or smectic, boundaries (even at a temperature of 0.1 degrees C above the phase separation in two phases). In polarized PCS experiments, we always see three relaxation processes well separated in time: one, very fast, with a relaxation time of the order of 10(-5) s; a second one with a relaxation time within the range 10(-2)-10(-3) s; and a last one, very slow, with a relaxation time of the order of 1 s. Both the fast and slow modes are independent of the wave vector magnitude, while the intermediate relaxation process is diffusive. In depolarized PCS experiments, the intermediate mode disappears and only the fast and slow relaxation processes remain, and they are independent of the magnitude of the wave vector. The diffusive mode is the classical diffusive mode, which is associated with the diffusion of polymer chains in all polymer solutions. The fast mode is due to the rotational diffusion of 4-cyano-4'-n-octyl-biphenyl (8CB) molecules close to polystyrene chains (transient network). Finally, we assign the slowest mode to reorientational processes of small aggregates of PS chains that are not dissolved in 8CB. 相似文献
3.
The -function method for evaluating effective actions is applied to an operator containing a potential localized on two parallel planes. This operator is characterized by a continuous spectrum and broken translation invariance. In this case, the -method leads to a divergent volume factor independent of the physical parameters. In a suitable regularization scheme, only the next to leading order term reproduces a physically interesting result. 相似文献
4.
Edith Chow Burkhard Raguse Karl‐H. Müller Lech Wieczorek Avi Bendavid James S. Cooper Lee J. Hubble Melissa S. Webster 《Electroanalysis》2013,25(10):2313-2320
The porosity of 1‐hexanethiol‐functionalised gold nanoparticle films was assessed and utilised as chemiresistor sensors. Electrochemical capacitance measurements showed that the accessibility of electrolytes of different ionic strengths into the pores depended on the thickness of the electric double layer formed. A large variation in capacitance was measured in 0.01–1000 mM NaClO4, implying a wide pore size distribution. The change in morphology of the nanoparticle films upon storage in air, water and ethanol for two weeks was investigated. There was a significant decrease in the electrochemical capacitance at high electrolyte concentrations for the ethanol‐stored films compared to the freshly‐prepared films suggesting a decrease in the number of small pores of radii in the range of 0.3–3 nm. This was further supported by optical topographical measurements where a decrease in the thickness of ethanol‐stored films was observed relative to the freshly‐prepared films. The porous nature of the nanoparticle films was found to have an effect on the chemical sensing behaviour. When used as chemiresistor sensors, for the detection of heptane in water, the ethanol‐stored films provided larger resistance changes and longer response times. This suggests that the more densely packed ethanol‐stored films provided more sites that enabled film swelling, and that diffusion of the analyte occurred through the narrower water‐filled pores. This demonstrates the effect of different storage conditions on film morphology and subsequently sensor response. 相似文献
5.
Andreas Wieczorek Hua Yang Brendan Roycroft Frank H. Peters Brian Corbett 《Optical and Quantum Electronics》2013,45(4):365-371
Polarization insensitive optical coupling of a large spot size input waveguide to a small spot size photodiode is achieved by the introduction of a transition waveguide. The coupling efficiency to the photodetector and the related absorption efficiency of the photodiode depend mainly on the refractive indices of the different InGaAsP layers. Waveguide alignments, waveguide widths and the n-contact etch depth do not influence the absorption efficiency relative to a 1-dB tolerance. 相似文献
6.
7.
Magdalena Rudowska Robert Wieczorek Alicja Kluczyk Piotr Stefanowicz Zbigniew Szewczuk 《Journal of the American Society for Mass Spectrometry》2013,24(6):846-856
The fragmentation of peptides containing quaternary ammonium group, but lacking easily mobilizable protons, was examined with the aid of deuterium-labeled analogs and quantum-chemical modeling. The fragmentation of oligoproline containing quaternary ammonium group involves the mobilization of hydrogens localized at α- and γ- or δ-carbon atoms in the pyrrolidine ring of proline. The study of the dissociation pattern highlights the unusual proline residue behavior during MS/MS experiments of peptides. 相似文献
8.
W. Wieczorek S. H. Chung J. R. Stevens 《Journal of Polymer Science.Polymer Physics》1996,34(17):2911-2917
The majority of investigations carried out on polymer(SINGLEBOND) salt systems have been on polyether electrolytes at moderate temperatures where such electrolytes exhibit macroscopic uniformity. Relatively little attention has been paid to the subambient temperature region where composite electrolytes based on polyethers exhibit much higher conductivities than their pure polyether electrolyte analogues. For all of the composite systems studied the conduction mechanism changes from one in which the ions are coupled to the polymer segmental relaxations to one in which the ions are decoupled and thermally activated ionic hopping produces higher conductivities than would be expected from ion-segmental coupling and higher than observed for the base polyether(SINGLEBOND) salt system. This change has been observed at temperatures between 10 and 80°C above the respective glass transition temperatures. The relationship between this interaction and these higher conductivities at subambient temperatures is explored and discussed. © 1996 John Wiley & Sons, Inc. 相似文献
9.
D. Kamińska A. Gajos E. Czerwiński D. Alfs T. Bednarski P. Białas C. Curceanu K. Dulski B. Głowacz N. Gupta-Sharma M. Gorgol B. C. Hiesmayr B. Jasińska G. Korcyl P. Kowalski W. Krzemień N. Krawczyk E. Kubicz M. Mohammed Sz. Niedźwiecki M. Pawlik-Niedźwiecka L. Raczyński Z. Rudy M. Silarski A. Wieczorek W. Wiślicki B. Zgardzińska M. Zieliński P. Moskal 《The European Physical Journal C - Particles and Fields》2016,76(8):445
10.
We compare the structures and energies of beta-strands, alpha-helices, and 3(10)-helices for capped polyalanines, acetyl(ala)(N)()NH(2), for values of N from 2 to 18, using completely optimized mixed DFT/AM1 calculations. Non-pairwise additive cooperativity is manifest from the variation of the relative energies, helical strain, dipole moments, and H-bond lengths of both types of helices, but especially for the alpha-helices. While the gas-phase 3(10)-helices are more stable for small polyalanines, largely due to the additional H-bond, the alpha-helices become relatively more stable as the polyalanines increase in size. 相似文献