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1.
2.
S. Park T. U. Kampen T. Kachel P. Bressler W. Braun D. R. T. Zahn 《Applied Surface Science》2002,190(1-4):376-381
The interaction of Ag and In with a thin film of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) was studied by near-edge X-ray absorption fine structure (NEXAFS). Upon Ag deposition on a PTCDA film of 20 nm thickness the relative intensities and lineshapes, as well as the angular dependence of the spectra remains unchanged, illustrating the formation of a chemically unreactive Ag/PTCDA interface. On the other hand, the adsorption of 0.3 nm In strongly decreases the intensity of the π* resonances in C and O K-edge NEXAFS spectra. This is attributed to a strong charge transfer between In and PTCDA, leading to a redistribution of the charge in the molecule. However, the absence of a strong shift or new features and negligible dependence of peak intensities corresponding to π* resonances on the In thickness indicate that the interaction between In and PTCDA is not accompanied by a covalent bond formation. 相似文献
3.
Zusammenfassung Es wird eine durch DNS ausgel?ste biologische Wirkkette diskutiert.
Durch DNS-Injektion lassen sich beim Warmblüter DNase-Aktivit?tserscheinungen hervorrufen.
DNasen bewirken in niedrigen Konzentrationsbereichen 10−13-10−5 g/ml eine Steigerung der Zellzahl.
In h?heren Konzentrationen wirken sie hemmend auf die Lebenst?tigkeit. Aufgrund dieser experimentellen Befunde ergibt sich
ein selbstregelnder Mechanismus.
Ausgeführt mit Mitteln der Deutschen Forschungsgemeinschaft. 相似文献
4.
2-Substituted secondary alcohol o-DPPB esters (o-DPPB=ortho-diphenylphosphanylbenzoyl) have been prepared and their o-DPPB-directed diastereoselective hydroformylation examined. It was found that the diastereoselectivity increased as a function of the steric demand of the substituents both at the stereogenic center and in the alkene 2-position. Hydrolytic cleavage of the o-DPPB group afforded-via the lactols 29-the corresponding lactones 30, the relative configurations of the vicinal stereogenic centers of which were ascertainable by 2D-NOESY spectroscopy. In addition, a crystal structure analysis of the hydroformylation product 2 d provided further confirmation of the relative configuration. Replacement of the ester carbonyl group of the o-DPPB by a methylene unit resulted in significantly worse diastereoselectivity in the course of the hydroformylation (34-->35), which indicates a decisive role for the ester carbonyl function. All the experimental observations were combined in a model of the origin of the 1,2-asymmetric induction during the title reaction. The key feature is the consideration of diastereomeric trigonal-bipyramidal rhodium-hydrido-olefin complexes I and II, capable on the basis of the Hammond postulate of acting as good models for the transition states of the selectivity-determining hydrometalation step. Investigation of these complexes by force-field methods indicated good correlation between theoretically predicted and experimentally determined diastereoselectivities. 相似文献
5.
The attachment of single ions to putative adsorption sites in the tails of collagen fibers is investigated by means of molecular dynamics simulations and discussed with respect to the very early steps of apatite/collagen biomineral formation. Our studies clearly demonstrate an increased flexibility of the tails of the triple‐helical collagen protein. Apart from the termini of the backbone, several side chains were also observed to be freely accessible to ion attachment from aqueous solution. The teleopeptide was systematically scanned for suitable adsorption sites for calcium, phosphate and fluoride ions. Association of these ions was then explored from potential of mean force calculations. The resulting energy profiles reveal a variety of favorable protein‐ion bonds and hint at the suitability of the collagen tails to promote apatite aggregation. 相似文献
6.
Magnesium is precipitated as hydroxide after elimination of interfering elements by means of ion-exchange procedures (phosphate, iron, trace elements) and masking with EDTA (calcium). The sample is applied in form of MgCl2 to the tungsten filament of an 1-filament-ion-source for surface ionization. 相似文献
7.
Ohne Zusammenfassung
Die R?ntgenuntersuchungen konnten wir im Physikalisch-Chemischen Institut der Universit?t Heidelberg durchführen. Herrn Dozenten
Dr. Borchert sind wir für das freundliche Entgegenkommen zu besonderem Dank verpflichtet. Herrn Prof. Dr. H. Nowotny, Wien,
danken wir für wertvolle Diskussionen. 相似文献
8.
9.
Ohne Zusammenfassung 相似文献
10.
M. Friedrich K. Hiller M. Wiemer T. Geßner D. R. T. Zahn 《Analytical and bioanalytical chemistry》1998,361(6-7):558-559
Basic investigations have been carried out on the characterization of different processing steps in bond preparation using
etched <111> faces of silicon wafers for the incidence of the infrared beam to a multiple internal reflection geometry. The
method is very sensitive to the surface coverage and interface. Surface activation by RCA cleaning yields an increase of water
coverage and a decrease of SiH and CH groups. The detection limit for an oxide layer between silicon wafers has been found
to be about 3 nm.
Received: 18 July 1997 / Revised: 15 August 1997 / Accepted: 19 August 1997 相似文献