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21.
Kay -Uwe Schaller 《Archiv der Mathematik》1982,38(1):496-500
Ohne Zusammenfassung 相似文献
22.
H. Brodowsky und H. -J. Schaller 《Colloid and polymer science》1977,255(9):925
Ohne Zusammenfassung 相似文献
23.
Dennis Jansen Johannes Gramüller Felix Niemeyer Torsten Schaller Matthias C. Letzel Stefan Grimme Hui Zhu Ruth M. Gschwind Jochen Niemeyer 《Chemical science》2020,11(17):4381
Organocatalysis has revolutionized asymmetric synthesis. However, the supramolecular interactions of organocatalysts in solution are often neglected, although the formation of catalyst aggregates can have a strong impact on the catalytic reaction. For phosphoric acid based organocatalysts, we have now established that catalyst–catalyst interactions can be suppressed by using macrocyclic catalysts, which react predominantly in a monomeric fashion, while they can be favored by integration into a bifunctional catenane, which reacts mainly as phosphoric acid dimers. For acyclic phosphoric acids, we found a strongly concentration dependent behavior, involving both monomeric and dimeric catalytic pathways. Based on a detailed experimental analysis, DFT-calculations and direct NMR-based observation of the catalyst aggregates, we could demonstrate that intermolecular acid–acid interactions have a drastic influence on the reaction rate and stereoselectivity of asymmetric transfer-hydrogenation catalyzed by chiral phosphoric acids.Supramolecular acid–acid interactions lead to competing monomeric and dimeric pathways in phosphoric acid catalysis – so that stereoselectivities depend on catalyst concentration. 相似文献
24.
A. Werthmüller A. Adamczak R. Jacot‐Guillarmod F. Mulhauser L.A. Schaller L. Schellenberg H. Schneuwly Y.‐A. Thalmann S. Tresch 《Hyperfine Interactions》1998,116(1-4):1-16
The charge exchange reaction of negative muons from the
atom to oxygen has been measured in gaseous mixtures of H2 + O2. The measurements were performed at three different relative oxygen concentrations ranging from 0.2% to 0.8% and total pressures 3.5–15 bar. A mean transfer rate of
, describing the transfer from the ground state of thermalized
atoms to oxygen, was determined. In order to investigate the energy dependence of the transfer rate, Monte Carlo simulations of the
thermalization and the muon transfer were carried out. The comparison of measured and simulated time spectra yielded an epithermal transfer rate
=3.9
1011 s-1 in the energy interval 0.12–0.22 eV. The analysis with the model of Two components shows that all measured time spectra can be reproduced with the same set of parameters. 相似文献
25.
26.
Rzepecki P Hochdörffer K Schaller T Zienau J Harms K Ochsenfeld C Xie X Schrader T 《Journal of the American Chemical Society》2008,130(2):586-591
Self-association of aminopyrazole peptide hybrid 1 leads to stacked nanorosettes. This remarkable, well-ordered structure obeys the laws of nucleic acid self-assembly. In a strictly hierarchical process, formation of aminopyrazole "base" triplets via a hydrogen bond network is accompanied by pi-stacking with a second rosette and final dimerization of two double rosettes to a four-layer superstructure, stabilized by a six-fold half-crown alkylammonium lock. The final complex is soluble in organic as well as in aqueous solution. It was characterized in the solid state by X-ray crystallography, in water by NMR spectroscopy, and in silico by quantum chemical shift calculation. All these methods provide strong evidence for the same hexameric complex geometry. Its structural features bear striking similarity to nucleic acid architectures and their peptidic counterparts, especially alanyl-PNA. The whole self-assembly process is highly solvent- and temperature-dependent and occurs with a high degree of cooperativity--no intermediates are observed. Formation and dissociation of the nanorosette, however, are kinetically slow. The limitation to a hexameric aggregate can be explained by six sterically demanding valine residues, whose replacement by alanines may result in formation of infinite fibers. 相似文献
27.
Shenghao Li Jing Lin Mareen Schaller Sylvio Indris Xin Zhang Torsten Brezesinski Ce-Wen Nan Shuo Wang Florian Strauss 《Angewandte Chemie (International ed. in English)》2023,62(50):e202314155
Superionic solid electrolytes (SEs) are essential for bulk-type solid-state battery (SSB) applications. Multicomponent SEs are recently attracting attention for their favorable charge-transport properties, however a thorough understanding of how configurational entropy (ΔSconf) affects ionic conductivity is lacking. Here, we successfully synthesized a series of halogen-rich lithium argyrodites with the general formula Li5.5PS4.5ClxBr1.5-x (0≤x≤1.5). Using neutron powder diffraction and 31P magic-angle spinning nuclear magnetic resonance spectroscopy, the S2−/Cl−/Br− occupancy on the anion sublattice was quantitatively analyzed. We show that disorder positively affects Li-ion dynamics, leading to a room-temperature ionic conductivity of 22.7 mS cm−1 (9.6 mS cm−1 in cold-pressed state) for Li5.5PS4.5Cl0.8Br0.7 (ΔSconf=1.98R). To the best of our knowledge, this is the first experimental evidence that configurational entropy of the anion sublattice correlates with ion mobility. Our results indicate the possibility of improving ionic conductivity in ceramic ion conductors by tailoring the degree of compositional complexity. Moreover, the Li5.5PS4.5Cl0.8Br0.7 SE allowed for stable cycling of single-crystal LiNi0.9Co0.06Mn0.04O2 (s-NCM90) composite cathodes in SSB cells, emphasizing that dual-substituted lithium argyrodites hold great promise in enabling high-performance electrochemical energy storage. 相似文献
28.
B. Gartner P. Ackerbauer M. Augsburger W.H. Breunlich M. Cargnelli D. Chatellard J.-P. Egger T. von Egidy F.J. Hartmann R. Jacot-Guillarmod E. Jeannet P. Kammel R.C. King A. Kosak B. Lauss J. Marton M. Mühlbauer F. Mulhauser C. Petitjean C. Piller W. Prymas L.A. Schaller L. Schellenberg H. Schneuwly W. Schott Y.A. Thalmann S. Tresch A. Werthmüller J. Zmeskal 《Hyperfine Interactions》1999,119(1-4):103-108
The energy and time distributions of the decay X-rays of excited, metastable, molecular (dμHe)*-resonances were measured. The comparison of the observed energy spectra with calculated ones suggests that decay from
the rotational state J = 1 dominates at the investigated conditions. The muon transfer rates from ground state deuterium to the helium isotopes
3He and 4He at low temperatures were determined from the time distributions of these spectra. Additionally, the temperature dependence
of the muon transfer rate was clearly established in deuterium / 4He mixtures.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
29.
Amido Ligands for the Synthesis of Polynuclear Lanthanoid Complexes By 1 : 1 reaction of LnBr3 with NaNHPh in THF the Rare-Earth Complexes [Ln2Br4(μ2-NHPh)2(thf)5] (Ln = Sm ( 1 ), Ln = Gd ( 2 )) with two bridging anilido ligands are obtained. In the system LnBr3/NaNHPh/(Me2SiO)3 the tetranuclear compounds [Ln4(μ4-O)(NHPh)3(OSiMe2NPh)6Na5(thf)7] · THF (Ln = Gd ( 3 ), Ln = Yb ( 4 )) can be built up. They have a central μ4-oxygene atom in the Ln4-tetrahedron. It has an oxa-dimethylsilyl-N-phenylamido ligand over all edges and an anilido ligand on three vertexes. By this reaction small amount of [Na4(thf)6Yb2(OSiMe2NPhSiMe2O)2(OSiMe2NPh)2(NHPh)2] ( 5 ) with a O- and N-bridged Yb–Na polyhedron and N-phenyl-bis(dimethylsilanolato)-ligands coordinating μ2-η2 with its oxygen atoms are obtained. Reaction of Lanthanideshalides with LiNHtBu leads to dimeric complexes. The formation of bridging oxasilylamido ligands is also observed. The compound [Li2Ln(OSiMe2NtBu)2(HNtBu)(thf)]2 (Ln=Sm ( 6 ), Gd ( 7 ) and Yb ( 8 )) contains now an O- and N-bridged Ln–Li polyhedron. (Crystal Data of 1–8 see ‘‘Inhaltsverzeichnis”︁”︁). 相似文献
30.