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101.
Positivity - In a Dedekind complete Riesz space, E, we show that if $$(P_n)$$ is a sequence of band projections in E then $$\begin{aligned} \limsup \limits _{n\rightarrow \infty } P_n - \liminf... 相似文献
102.
J. P. Dufour S. Beraud-Sudreau R. Del Moral H. Emmermann A. Fleury F. Hubert C. Poinot M. Pravikoff J. Frehaut M. Beau A. Bertin G. Giraudet A. Huck G. Klotz C. Miehe C. Richard-Serre H. Delagrange 《Zeitschrift für Physik A Hadrons and Nuclei》1984,319(2):237-238
The new beta-delayed neutron emitter15B has been observed. The measured half-life is 11 ms ±1 ms and limits have been set on other decay channels: P0n<5%, P2n<1.5%. The beta emitter12Be has been separated, unambiguously identified, and its half-life has been measured to be 24±1 ms. 相似文献
103.
104.
Agnello M Belli G Bendiscioli G Bertin A Botta E Bressani T Bruschi M Bussa MP Busso L Calvo D Cereda B Cerello PG Cicalò C Corradini M Costa S De Castro S Donzella A Feliciello A Ferrero L Filippi A Filippini V Fontana A Galli D Garfagnini R Giacobbe B Gianotti P Grasso A Guaraldo C Iazzi F Lanaro A Lodi Rizzini E Lucherini V Marcello S Marconi U Masoni A Minetti B Montagna P Morando M Nichitiu F Panzieri D Pauli G Piccinini M Puddu G Rossetto E Rotondi A Rozhdestvensky AM Saino A Salvini P 《Physical review letters》1995,74(3):371-374
105.
Le Bouder T Maury O Bondon A Costuas K Amouyal E Ledoux I Zyss J Le Bozec H 《Journal of the American Chemical Society》2003,125(40):12284-12299
The synthesis, photophysical and nonlinear optical properties of several new multi-octupolar tris(bipyridine) ruthenium complexes are reported. The preparation on these complexes is based on the initial construction of multipodal 4,4'-dialkylaminostyryl-2,2'-bipyridine ligands (DAAS-bpy). Thermally stable polyimides featuring octupolar ruthenium trisbipyridyl complexes have been readily obtained by a polycondensation reaction. The controlled coordination strategy of dipodal and tripodal bipyridines to ruthenium(II) has also been successfully used to build bimetallic, trimetallic as well as the first metallodendrimer made of seven metallo-octupoles. These polymetallic species exhibit very intense absorption bands in the visible and long-lived luminescence. The quadratic NLO-susceptibilities beta of these macromolecules have been characterized by harmonic light scattering at 1.91 microm and compared with those of the corresponding monometallic species. The NLO studies clearly demonstrates a quasi-supramolecular ordering in the metallodendrimer. 相似文献
106.
Here, we report the solid-phase synthesis of a 17-mer cyclopeptide which is expected to have anti-angiogenic properties. The peptidic synthesis is performed on an allyldimethylsilyl polystyrene support loaded by metathesis with a conveniently functionalized d-Tyrosine amino acid. The linear peptide was assembled by standard Fmoc chemistry and on-resin cyclization was enabled after selective deprotection of the C-terminal group with 2% hydrazine/DMF at room temperature. Final cleavage was realized under mild acidic conditions allowing to obtain a cyclopeptide under partially protected form. 相似文献
107.
Dr. Dominique Marion Dr. Diego F. Gauto Isabel Ayala Karine Giandoreggio-Barranco Dr. Paul Schanda 《Chemphyschem》2019,20(2):276-284
Studying protein dynamics on microsecond-to-millisecond (μs-ms) time scales can provide important insight into protein function. In magic-angle-spinning (MAS) NMR, μs dynamics can be visualized by rotating-frame relaxation dispersion experiments in different regimes of radio-frequency field strengths: at low RF field strength, isotropic-chemical-shift fluctuation leads to “Bloch-McConnell-type” relaxation dispersion, while when the RF field approaches rotary resonance conditions bond angle fluctuations manifest as increased rate constants (“Near-Rotary-Resonance Relaxation Dispersion”, NERRD). Here we explore the joint analysis of both regimes to gain comprehensive insight into motion in terms of geometric amplitudes, chemical-shift changes, populations and exchange kinetics. We use a numerical simulation procedure to illustrate these effects and the potential of extracting exchange parameters, and apply the methodology to the study of a previously described conformational exchange process in microcrystalline ubiquitin. 相似文献
108.
Castro-Perez J Plumb R Granger JH Beattie I Joncour K Wright A 《Rapid communications in mass spectrometry : RCM》2005,19(6):843-848
The field of drug metabolism has been revolutionized by liquid chromatography/mass spectrometry (LC/MS) applications with new technologies such as triple quadrupoles, ion traps and time-of-flight (ToF) instrumentation. Over the years, these developments have often relied on the improvements to the mass spectrometer hardware and software, which has allowed users to benefit from lower levels of detection and ease-of-use. One area in which the development pace has been slower is in high-performance liquid chromatography (HPLC). In the case of metabolite identification, where there are many challenges due to the complex nature of the biological matrices and the diversity of the metabolites produced, there is a need to obtain the most accurate data possible. Reactive or toxic metabolites need to be detected and identified as early as possible in the drug discovery process, in order to reduce the very costly attrition of compounds in late-phase development. High-resolution, exact mass measurement plays a very important role in metabolite identification because it allows the elimination of false positives and the determination of non-trivial metabolites in a much faster throughput environment than any other standard current methodology available to this field. By improving the chromatographic resolution, increased peak capacity can be achieved with a reduction in the number of co-eluting species leading to superior separations. The overall enhancement in the chromatographic resolution and peak capacity is transferred into a net reduction in ion suppression leading to an improvement in the MS sensitivity. To investigate this, a number of in vitro samples were analyzed using an ultra-performance liquid chromatography (UPLC) system, with columns packed with porous 1.7 mum particles, coupled to a hybrid quadrupole time-of-flight (ToF) mass spectrometer. This technique showed very clear examples for fundamental gains in sensitivity, chromatographic resolution and speed of analysis, which are all important factors for the demands of today's HTS in discovery. 相似文献
109.
110.
Modifications of the known route to camphosultam led to an easy two-step process. The unique intermediate is simply isolated by filtration. The overall yield is 66% on a hundred gram scale. 相似文献