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1.
The measured particle ratios in central heavy-ion collisions are investigated within a chemical and thermal equilibrium chiral SU(3) σ?ω approach. Contrary to the commonly adopted non-interacting gas calculations, the chiral SU(3) model predicts modified effective hadron masses and effective chemical potentials in the medium and a transition to a chirally restored phase at high temperatures or chemical potentials. the influence of three different types of phase transitions is investigated. We show that the deduced freeze-out values considerably depend on the underlying model while the quality of the fit is approximately the same.  相似文献   
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3.
Excited states of73Se have been investigated up to spin, 21/2 using techniques of in-beamγ-ray spectroscopy in connection with the70Ge(α, n) reaction. Mean lifetimes of 12 levels have been determined applying Doppler-shift andγ-RF-methods. Five different bands have been identified that reflect a variety of different excitation modes. The decoupled 9/2+ band is likely to correspond to an oblate deformation while the 5/2+ band is interpreted as a strongly coupled prolate band built on the Nilsson configuration [422] 5/2+. The 3/2? band is a strongly coupled band built on the [301] 3/2} configuration.Nuclear reactions:70Ge(α,n),E=14, 16, 18, 19, 20MeV; measuredE γ,I γ,σ(E γ,θ),γγ-coin, linear polarization, DSA,γ(t).75Se deduced levels,I, π, τ, δ(E2/M1), B(σλ). Enriched targets, Ge detectors.  相似文献   
4.
An (α, 2nγ) in-beam study of excited states in 142Nd revealed 27 new levels on top of the 6+ isomer. Nanosecond lifetimes were found for two levels. The measured excitation energies were compared with spherical shell-model predictions obtained from suitably truncated model spaces.  相似文献   
5.
A series of ferrocene-containing polymeric azines and polymeric Schiff bases have been synthesized by means of acid-catalyzed solution polycondensations. The molecular structures of the polymers synthesized have been determined, and information concerning their thermal behavior has been obtained. Comparative thermal stabilities of the products of polymerization of aliphatic and aromatic diamines with 1,1′-diformylferrocene and 1,1′-diacetylferrocene were investigated by thermogravimetric analysis both in air and in an inert atmosphere. In the inert atmosphere, initial weight loss due to thermal stress did not occur below 300°C in all cases, and in many cases 50–70% residue of polymer sample remained at 700°C. The use of a fluorinated diamine led to the synthesis of a polymer which did not exhibit any significant enhancement of thermal properties. Investigation of the polymer products by direct inlet mass spectroscopy led to the observation that several of the systems contained significant amounts of cyclic dimers, although linear polymers were the major products in most cases. Extraction of the cyclic dimers followed by molecular weight determination by vapor phase osmometry confirmed their molecular structures.  相似文献   
6.
Isotope-labeled drug molecules may be useful for probing by NMR spectroscopy the conformation of ligand associated with biological hosts such as membranes and proteins. Triple-labeled [7,9,19-(13)C(3)]-vitamin D(3) (56), its 25-hydroxylated and 1 alpha,25-dihydroxylated metabolites (58 and 68, respectively), and other labeled materials have been synthesized via coupling of [9-(13)C]-Grundmann's ketone 39 or its protected 25-hydroxy derivative 43 with labeled A ring enyne fragments 25 or 26. The labeled CD-ring fragment 39 was prepared by a sequence involving Grignard addition of [(13)C]-methylmagnesium iodide to Grundmann's enone 28, oxidative cleavage, functional group modifications leading to seco-iodide 38, and finally a kinetic enolate S(N)2 cycloalkylation. The C-7,19 double labeling of the A-ring enyne was achieved by the Corey-Fuchs/Wittig processes on keto aldehyde 11. By employing these labeled fragments in the Wilson-Mazur route, the C-7,9,19 triple-(13)C-labeled metabolites 56, 58, and 68 as well as other (13)C-labeled metabolites have been prepared. In an initial NMR investigation of one of the labeled metabolites prepared in this study, namely [7,9,19-(13)C(3)]-25-hydroxyvitamin D(3) (58), the three (13)C-labeled carbons of the otherwise water insoluble steroid could be clearly detected by (13)C NMR analysis at 0.1 mM in a mixture of CD(3)OD/D(2)O (60/40) or in aqueous dimethylcyclodextrin solution and at 2 mM in 20 mM sodium dodecyl sulfate (SDS) aqueous micellar solution. In the SDS micellar solution, a double half-filter NOESY experiment revealed that the distance between the H(19Z) and H(7) protons is significantly shorter than that of the corresponding distance calculated from the solid state (X-ray) structure of the free ligand. The NMR data in micelles reveals that 58 exists essentially completely in the alpha-conformer with the 3 beta-hydroxyl equatorially oriented, just as in the solid state. The shortened distance (H(19Z))-H(7)) in micellar solutions as compared to that in the solid state is most easily rationalized on the basis that the 5(10)-torsion angle in 58 is decreased in micellar solutions as compared to that in the solid state.  相似文献   
7.
Selected benzoic acid derivatives and related substances were used as additives to 2,5-dihydroxybenzoic acid (2,5DHB) and the performance of the mixtures in matrix-assisted laser desorption/ionization mass spectrometry was investigated. Using benzoic acid derivatives substituted at position 2 and/or 5 or related substances as a co-matrix in the 1–10% range with 2,5DHB results in improved ion yields and signal-to-noise ratio of analyte molecules, especially for the high-mass range. The enhanced performance is prominent for 2-hydroxy-5-methoxybenzoic acid and exists for both proteins and oligosaccharides. It is suggested that the improvement is caused by a disorder in the 2,5DHB crystal lattice allowing ‘softer’ desorption. Charge transfer from matrix ions to additive molecules at the expense of analyte ionization gives a simple explanation for the deteriorating effects of some tested additives.  相似文献   
8.
Zusammenfassung Die Methode von Bonsels u. Linnemann [1] zur Bestimmung von FeII und MnIII lieferte bei der Überprüfung falsche Ergebnisse. Die Ursache liegt darin, daß sich der Blindwert des Azides in Gegenwart von Mn-Ionen erheblich erhöht und in der Siedehitze eine Reaktion zwischen MnIII und CrIII abläuft. Da eine Auflösung selbst fein pulverisierter Ferrite in dem mitgeteilten Lösungsgemisch nur in der Siedehitze erfolgt, ist eine Bestimmung von FeII und MnIII in Ferriten nach dieser Methode nicht möglich.
Summary The method for the determination of FeII and MnIII in manganese ferrites by Bonsels and Linnemann [1] was examined. It was found that the consumption of NaN3, used for the reduction of MnIII and effecting in a second (not wanted) reaction the reduction of Cr2O7 2–, is essentially increased by the presence of MnII and causes an error in the determination of FeII. The second error is the reaction between MnIII and CrIII at boiling temperature. On account of the necessity to dissolve the ferrites with the acid mixture at boiling temperature the determination of MnIII and FeII is not possible.


Herrn Dr. P. Kleinert vom Institut für Magnetische Werkstoffe danken wir an dieser Stelle für wertvolle Diskussionsbeiträge und das bei der Durchführung der Arbeit gezeigte Interesse.  相似文献   
9.
A series of unsymmetrical 1,2-bis(phosphino)ethanes R(2)PCH(2)CH(2)PR'(2) and 1-arsino-2-phosphinoethanes R(2)AsCH(2)CH(2)PR'(2) mainly with bulky substituents R and R' were prepared from the cyclic sulfate by stepwise cleavage of the carbon-oxygen bonds by LiPR(2) and LiPR'(2) or LiAsR(2) and LiPR'(2), respectively. Analogously, racemic mixtures of R(2)PCH(2)CH(Me)PPh(2)(R =iPr, Cy ) as well as the enantiomers (R)-, (R)- and (R)-tBu(2)PCH(2)CH(Me)PPh(2)(R)- were obtained from the corresponding unsymmetrical cyclic sulfates and (S)-. On a similar route, the racemates of the 1,3-bis(phosphino)propanes R(2)PCH(2)CH(2)CH(Me)PPh(2)(R =iPr, tBu ), optically pure (R)- and (S,S)-iPr(2)PCH(Me)CH(2)CH(Me)PPh(2)(S,S)- were prepared. The reaction of [[RhCl([small eta](4)-C(8)H(12))](2)] with chelating ligands L-L, where L-L is R(2)PCH(2)P(men)(2)(R =iPr, Ph; men =(1S,2R,5S)-menthyl), Cy(2)AsCH(2)P(men)(2), or (R)-, (R)-, (R)-, (R)- and (S,S)-, in the presence of AgPF(6), gave the complexes [Rh(eta(4)-C(8)H(12))(L-L)]PF(6) which were used as pre-catalysts in the hydrogenation of the methyl ester of alpha-acetamidocinnamic acid (ACM). Depending on L-L, the solvent, the temperature and the pressure of H(2), optical yields of up to 69% ee were achieved. For two of the rhodium complexes, and, the molecular structures were determined by X-ray crystallography.  相似文献   
10.
After the application of simulated digestive fluids (gastric and intestinale fluid) as extraction solutions, AAS and differential pulse anodic-stripping voltammetry (DPASV) were used as analytical methods in combination with ion-exchange procedures for the determination of zinc species and total zinc contents. The ion exchange procedure and the shifting of electrochemical potentials as well as changes of the calibration slope after standard addition in the polarographic analysis allowed discriminating statements with regard to a possible resorption of zinc. On the basis of these methods, a strategy is presented for in vitro investigations of the bioavailability of zinc in foodstuffs.  相似文献   
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