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J. Moche S. J. Rubaschkin S. M. Gutman S. L. Yovanovitch W. L. Miller B. L. Clarke L. A. Wooten C. Luke A. Winkel und G. Proske 《Fresenius' Journal of Analytical Chemistry》1938,112(7-8):266-271
Ohne Zusammenfassung 相似文献
3.
The preparation and application of a new series of chiral ionic liquids are described. The salts are based on imidazolinium cations. Some of the cations also incorporated an axial chirality at the C(2) position next to the central chirality. These cations display a very high rotational barrier along the arene–imidazolinium axis. Furthermore, an analogue with a chiral anion was prepared. The salts have low melting points. Their potential as solvents and as chiral shift reagents was explored, resulting for the first time in an example of a chiral ionic liquid as a shift reagent for a neutral compound. 相似文献
4.
We construct random locally compact real trees called Lévy trees that are the genealogical trees associated with continuous-state
branching processes. More precisely, we define a growing family of discrete Galton–Watson trees with i.i.d. exponential branch
lengths that is consistent under Bernoulli percolation on leaves; we define the Lévy tree as the limit of this growing family
with respect to the Gromov–Hausdorff topology on metric spaces. This elementary approach notably includes supercritical trees
and does not make use of the height process introduced by Le Gall and Le Jan to code the genealogy of (sub)critical continuous-state
branching processes. We construct the mass measure of Lévy trees and we give a decomposition along the ancestral subtree of
a Poisson sampling directed by the mass measure.
T. Duquesne is supported by NSF Grants DMS-0203066 and DMS-0405779. M. Winkel is supported by Aon and the Institute of Actuaries,
EPSRC Grant GR/T26368/01, le département de mathématique de l’Université d’Orsay and NSF Grant DMS-0405779. 相似文献
5.
Ole E. Barndorff-Nielsen Neil Shephard Matthias Winkel 《Stochastic Processes and their Applications》2006
In this paper we provide a systematic study of how the probability limit and central limit theorem for realised multipower variation changes when we add finite activity and infinite activity jump processes to an underlying Brownian semimartingale. 相似文献
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Molar extinction coefficients of some carbohydrates viz. l-arabinose (C5H10O5), d-glucose (C6H12O6), d-mannose (C6H12O6), d-galactose (C6H12O6), d(-) fructose (C6H12O6) and maltose (C12H24O12) in aqueous solutions have been determined at 81, 356, 511, 662, 1173 and 1332 keV by gamma ray transmission method in a
narrow beam good geometry set-up. These coefficients have been found to depend upon the photon energy following a 4-parameter
polynomial. These extinction coefficients for different sugars having the same molecular formula have same values varying
within experimental uncertainty. Within concentration ranges studied, Beer-Lambert law is obeyed very well. 相似文献
8.
Ingrid Kohl Dr. Katrin Winkel Marion Bauer Klaus R. Liedl Prof. Dr. Thomas Loerting Prof. Dr. Erwin Mayer Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(15):2690-2694
What's the matter? The laboratory Raman spectra for carbonic acid (H2CO3), both for the β‐polymorph and its amorphous state, are required to detect carbonic acid on the surface of the pole caps of Mars in 2009, when the Mars Microbeam Raman Spectrometer lands on the planet. The picture shows a martian crater with ice of unknown composition, possibly containing carbonic acid (image adapted from DLR, with permission from ESA, DLR, and FU Berlin –‐G. Neukum).
9.
p palan BS 《Physical review letters》1987,58(16):1597-1599
10.
Winkel K Hage W Loerting T Price SL Mayer E 《Journal of the American Chemical Society》2007,129(45):13863-13871
Layers of glassy methanolic (aqueous) solutions of KHCO3 and HCl were deposited sequentially at 78 K on a CsI window, and their reaction on heating in vacuo in steps from 78 to 230 K was followed by Fourier transform infrared (FTIR) spectroscopy. After removal of solvent and excess HCl, IR spectra revealed formation of two distinct states of amorphous carbonic acid (H2CO3), depending on whether KHCO3 and HCl had been dissolved in methanol or in water, and of their phase transition to either crystalline alpha- or beta-H2CO3. The main spectral features in the IR spectra of alpha- and beta-H2CO3 are observable already in those of the two amorphous H2CO3 forms. This indicates that H-bond connectivity or conformational state in the two crystalline phases is on the whole already developed in the two amorphous forms. The amorphous nature of the precursors to the two crystalline polymorphs is confirmed using powder X-ray diffraction. These diffractograms also show that alpha- and beta-amorphous H2CO3 are two distinct structural states. The variety of structural motifs found within a few kJ/mol in a computational search for possible crystal structures provides a plausible rationalization for (a) the observation of more than one amorphous form and (b) the retention of the motif observed in the amorphous form in the corresponding crystalline form. The polyamorphism inferred for carbonic acid from our FTIR spectroscopic and powder X-ray diffraction studies is special since two different crystalline states are linked to two distinct amorphous states. We surmise that the two amorphous states of H2CO3 are connected by a first-order-like phase transition. 相似文献