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51.
For the anisotropic Universe filled with massless vector field in the General Relativity frame we obtain bouncing solution for one of scale factors. We obtain the Universe with finite maximal energy density, finite value of R,RμνRμν,RμναβRμναβ and non-zero value of a scale factor for directions transverse to a vector field. Such a bounce can be also obtained for a massive vector field with kinetic initial conditions, which gives isotropic low energy limit. We discuss the existence of a bounce for a massless vector field with additional matter fields, such as cosmological constant or dust. We also discuss bouncing solution for massless vector field domination in n+2-dimensional space-time. 相似文献
52.
P. Konieczka M. Prokopowicz B. Zygmunt J. F. Biernat J. Namieśnik 《Chromatographia》2000,51(1):S249-S260
A new approach to the preparation of standard gaseous mixtures based on thermal decomposition of surface compounds, has been
reviewed. The method is used to prepare standard mixtures containing volatile analytes such as thiols, isothiocyanates, carbon
monoxide, carbon dioxide, ammonia, amines, ethylene and methyl chloride. The method enables the preparation of the standard
immediately before a calibration step. It is specially useful for the generation of standard mixtures containing volatile,
malodorous, unstable and toxic compounds.
Presented at Balaton Symposium on High Performance Separation Methods, Siófok, Hungary, September 1–3, 1999 相似文献
53.
Badral Gansukh Qiuyue Zhang Zygmunt Flisak Tongling Liang Yanping Ma Wen-Hua Sun 《应用有机金属化学》2020,34(4):e5471
The five unsymmetrical 2-[1-(2,4-dibenzhydryl-6-chlorophenylimino)ethyl]-6-[1-(arylimino)ethyl]pyridine compounds (aryl: 2,6-Me2Ph L1 , 2,6-Et2Ph L2 , 2,6-iPr2Ph L3 , 2,4,6-Me3Ph L4 and 2,6-Et2–4-MePh L5 ) were prepared and characterized with FT-IR and 1H/13C NMR spectroscopy as well as elemental analysis. The treatment of L1 – L5 with CrCl3·3THF affords the corresponding chromium chloride complexes ( Cr1 – Cr5 ) in excellent yields. The molecular structures of Cr2 and Cr3 characterized by X-ray diffraction show a distorted octahedral geometry with three nitrogen atoms and three chlorine atoms around the metal center. On activation with either MAO or MMAO, Cr1 – Cr5 collectively display high activity (up to 14.96 × 106 g (PE) mol−1 (Cr) h−1 at 60 °C) affording highly linear polyethylene with low molecular weight distribution (Mw/Mn) ranging from 1.06 to 2.81. An in-depth catalytic evaluation of Cr1 was conducted in order to investigate how the cocatalyst type and its amount, reaction temperature and polymerization time affect the catalytic activities and polymer properties. 相似文献
54.
We consider a class of algebras whose Auslander-Reiten quivers have starting components that are not generalized standard.
For these components we introduce a generalization of a slice and show that only in finitely many cases (up to isomorphism)
a slice module is a tilting module.
The first named author was supported by the Polish Scientific Grant KBN No 1 P03A 018 27 相似文献
55.
Henryk Malak Ignacy Gryczynski Joseph R. Lakowicz Gerald J. Meyers Felix N. Castellano 《Journal of fluorescence》1997,7(2):107-112
We examined the intensity and anisotropy decays of DNA labeled with two ruthenium metalligand complexes, [Ru(bpy)2(dppz)]2+ and [Ru(phe)2(dppz)]2+. Both complexes display high emission anisotropies in the absence of rotational diffusion, making them suitable probes for
rotational motions. When bound to DNA, these complexes display decay times as long as 294 ns, providing long-lived probes
of DNA dynamics. The decay times of both complexes were rather insensitive to dissolved oxygen. We examined anisotropy decays
of these complexes bound to B-form DNA. The anisotropy decays revealed correlation times near 10, 50, and several hundred
nanoseconds, suggesting that these probes are sensitive to a wide range of DNA motions. The use of metalligand complexes should
allow resolution of both the torsional and bending motions of DNA, the latter of which has been mostly inaccessible using
shorter-lived fluorescent probes bound to DNA.
Dedicated to Professor Robert F. Steiner upon his retirement 相似文献
56.
Zygmunt Bak 《Czechoslovak Journal of Physics》2003,53(1):5-9
We consider interlayer magnetic coupling in a superlattice and/or overlayer in the case when spacer layer has the tendency towards formation of the helical spin density wave. Within phenomenological Landau-Ginzburg approach we show that the mutual interplay of the SDW and interlayer coupling spin polarization can lead to the helical interlayer coupling. When surface anisotropy is accounted for the effective interaction mimics interlayer biquadratic coupling. 相似文献
57.
Joseph R. Lakowicz Bogumil Zelent Ignacy Gryczynski Józef Kuba Michael L. Johnson 《Photochemistry and photobiology》1994,60(3):205-214
Abstract We used GHz frequency-domain fluorometry to investigate the time-dependent intensity decays of N -acetyl -L-trytophanamide (NATA) when collisionally quenched by acrylamide in propylene glycol at 20°C. The intensity decays of NATA became increasingly heterogeneous in the presence of acrylamide. The NATA intensity decays were not consistent with the Collins-Kimball radiation boundary condition (RBC) model for quenching. The steady-state Stern-Volmer plots show significant upward curvature. At low temperature in vitrified propylene glycol (-60%), where translational diffusion cannot occur during the lifetime of the excited state, quenching of NATA by acrylamide was observed. The Smoluchowski and RBC quenching models do not predict any quenching in the absence of translational diffusion. Hence, these frequency-domain and steady-state data indicate a through-space quenching interaction between NATA and acrylamide. The rate for quenching of NAT A by acrylamide appears to depend exponentially on the fluorophore-quencher separation distance. Comparison of the time-resolved and steady-state data provides a sensitive method to determine the distance dependence of the fluorophore-quencher interaction. The distance-dependent rate of quenching also explains the upward curvature of the Stern-Volmer plot, which is often observed for quenching by acrylamide. These results suggest that the distance-dependent quenching rates need to be considered in the interpretation of quenching data of proteins by acrylamide. 相似文献
58.
Time-resolved fluorescence intensity and anisotropy decay data were obtained for ribonuclease T1 entrapped in bis(2-ethylhexyl) sodium sulfosuccinate/heptane reverse micelles, as a function of the size of the inner water pool at neutral pH. Data have been presented previously to show that this protein retains its native structure and undergoes reversible thermal unfolding in these reverse micelles (Shastry and Eftink,Biochemistry
36, in press). The fluorescence decay of entrapped protein is similar to that for the protein in buffer. The rotational correlation time of entrapped ribonuclease T1 is found to be longer than that in buffer; this rotational correlation time decreases with increasing size of the water pool but is still over twice the value for the protein in buffer for the largest size of water pool investigated, indicating an increased microviscosity within the reverse micelle. Thermal unfolding of the protein results in a significant decrease in the rotational correlation time of the entrapped proteins, consistent with the protein being unfolded but not interacting with the inner surfactant wall of the reverse micelle.Nomenclature i
Amplitude of component i associated with fluorescence decay i
- i
Fractional intensity associated with fluorescence decay time i
-
Rotational correlation time gi Amplitude of component i associated with anisotropy decay i
- max
Fluorescence emission maximum
- ro
Fundamental anisotropy of an immobilized fluorophore
- i
Fluorescence lifetime of component i
- Wo
Ratio of water molecules per detergent molecules in a reverse micelle 相似文献
59.
We measured the linear dichroism of several metalloporphyrins embedded in stretched polyvinyl alcohol (PVA) films to estimate the orientation of the absorption transition moments, which in hemoproteins are relevant to the radiationless energy transfer between tryptophan and heme. The metalloporphyrins were derivatives of protoporphyrin IX (PPIX), namely Fe3+ -PPIX (ferric-heme) and Fe2+ CO-PPIX (CO-heme), Mg-PPIX (Mg-heme) and Zn-PPIX (Zn-heme). Measurements were conducted between 300 and 700 nm. In all cases the linear dichroism was wavelength dependent, indicating the presence of several transition moments with different orientations. We focused our attention on the near-UV (300–380 nm) and Soret (380450 nm) absorption bands. Deconvolution in terms of Gaussian components gave three components between 380 and 450 nm and only one in the 300–380 nm region. Deconvolution of the near-UV and Soret spectra of oxy-, deoxy- and carbonmonoxyhemoglobin gave very similar results, suggesting a very similar orientation of the various transition moments in the free and protein-embedded hemes. It should be stressed that the single 300–380 nm band is the only one responsible for the overlap integral that regulates the energy transfer from tryptophan to heme in hemoproteins (Gryczynski et al., Biophys. J . 63, 648–653, 1992). The dichroism of this single band indicated that its transition moment is oriented at about 60 from the α-γ meso-axis of the heme moiety. We conclude that the heme should be considered a linear oscillator when it acts as acceptor of energy transfer from tryptophans. 相似文献
60.
Surface-enhanced fluorescence of fluorescein-labeled oligonucleotides capped on silver nanoparticles 总被引:1,自引:0,他引:1
Zhang J Malicka J Gryczynski I Lakowicz JR 《The journal of physical chemistry. B》2005,109(16):7643-7648
Tiopronin monolayer-protected silver nanoparticles with different core sizes (average diameter = 2, 5, 20 nm) were prepared by using different mole ratios of silver nitrate/tiopronin. Ligands on the silver particles were partially displaced by fluorescein-labeled thiolate single-stranded oligonucleotides or their complementary unlabeled oligonucleotides through ligand exchange. The fluorophores on silver particles showed a surface-enhanced fluorescence (SEF) dependent on the size of metallic cores. The particles could be coupled through hybridizations of oligonucleotides bound on the particles. The coupled particles were aggregated due to multiple displacements of oligonucleotides on each particle, resulting in stronger SEF. The dye-labeled oligonucleotides were assembled on the silver islands on the solid substrate, and the complementary oligonucleotide-displaced particles were coupled via oligonucleotide hybridization. The couplings between particles and islands resulted in an obvious fluorescence enhancement. 相似文献