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排序方式: 共有86条查询结果,搜索用时 15 毫秒
1.
Dr. Tarun Kumar Yan Yang Sirine Sghaier Dr. Yassir Zaid Dr. Xavier F. Le Goff Dr. Elodie Rousset Dr. Fabien Massicot Dr. Dominique Harakat Agathe Martinez Dr. Marc Taillefer Prof. Laurent Maron Prof. Jean-Bernard Behr Dr. Florian Jaroschik 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(12):4016-4021
The development of new fluorine-containing building blocks and their efficient synthetic access is currently a challenging research field. Herein, the highly regio- and stereoselective addition of a large range of aldehydes onto trifluoromethylated benzofulvenes was achieved using a simple La/I2/DIBAL-Cl system via a selective C−F bond activation process. This versatile methodology provided homodienyl alcohols bearing a terminal CF2-alkene with potential further applications, as shown by the dehydration to the first benzofulvenes carrying a difluorovinyl group. In addition, for certain electron-poor aldehydes, unprecedented ipso substitution of the CF3 group in a diene was observed, which, according to DFT studies, is related to the presence of the large, Lewis-acidic lanthanum metal. 相似文献
2.
This paper presents a new method to obtain chemical equilibrium properties of detonation products mixtures including a solid carbon phase. In this work, the solid phase is modelled through a mesoparticle immersed in the fluid, such that the heterogeneous character of the mixture is explicitly taken into account. Inner properties of the clusters are taken from an equation of state obtained in a previous work, and interaction potential between the nanocluster and the fluid particles is derived from all-atoms simulations using the LCBOPII potential (Long range Carbon Bond Order Potential II). It appears that differences in chemical equilibrium results obtained with this method and the "composite ensemble method" (A. Hervouet et al., J. Phys. Chem. B, 2008, 112.), where fluid and solid phases are considered as non-interacting, are not significant, underlining the fact that considering the inhomogeneity of such system is crucial. 相似文献
3.
The 13P and 13C spectra of the triply 13C labelled molecules (CH3)3P, (CH3)3PO, (CH3)3PS and (CH3)3PSe oriented in a nematic phase are reported. The CPC bond angles have been measured. The 13P chemical shift tensor shows a large anisotropy except in the case of (CH3)3P. The abnormal large value observed for the PSe bond length suggests a large anisotropy of the 1J(PSe) spin coupling. 相似文献
4.
5.
Roger E. Behrend Paul A. Pearce Valentina B. Petkova Jean-Bernard Zuber 《Nuclear Physics B》2000,570(3):525-589
We develop further the theory of Rational Conformal Field Theories (RCFTs) on a cylinder with specified boundary conditions emphasizing the role of a triplet of algebras: the Verlinde, graph fusion and Pasquier algebras. We show that solving Cardy's equation, expressing consistency of a RCFT on a cylinder, is equivalent to finding integer valued matrix representations of the Verlinde algebra. These matrices allow us to naturally associate a graph G to each RCFT such that the conformal boundary conditions are labelled by the nodes of G. This approach is carried to completion for sl(2) theories leading to complete sets of conformal boundary conditions, their associated cylinder partition functions and the A-D-E classification. We also review the current status for WZW sl(3) theories. Finally, a systematic generalisation of the formalism of Cardy–Lewellen is developed to allow for multiplicities arising from more general representations of the Verlinde algebra. We obtain information on the bulk–boundary coefficients and reproduce the relevant algebraic structures from the sewing constraints. 相似文献
6.
We consider the lagrangian form of a q-state generalization of Ising gauge theories with matter fields in d = 3 and 4 dimensions. The theory is exactly soluble in the limit q → ∞ and corrections are easily calculable in power series in . Extrapolating the series for the free energies and latent heats by the method of Padé approximants, we have constructed the phase diagrams for all values of q. Our results agree well with known results for pure spin systems and, for the case q = 2, with Ising Monte Carlo data. 相似文献
7.
8.
Andr Cogne Afonso G. Guimaraes Jean Martin Robert Nardin Jean-Bernard Robert Wojciech J. Stec 《Magnetic resonance in chemistry : MRC》1974,6(12):629-635
The 1H NMR spectra of several 1,3,2-dioxaphosphorinanes bearing an extracyclic P? N bond have been analysed. The 3J(POCH) couplings are strongly dependent upon the orientation of the bond around the phosphorus atom. Depending upon the nature of the bonds attached to the nitrogen atom, the dioxaphosphorinane ring may adopt either a fixed chair conformation with the P? N bond in the axial or equatorial orientation, or it may be in equilibrium between two chair conformations where the P? N bond is alternately axial or equatorial. The equilibrium is fast on the NMR time scale. 相似文献
9.
10.
Grard Gouesbet Patrick Gougeon Jean-Noël Le Toulouzan Massamba Thioye Jean-Bernard Guidt 《Particle & Particle Systems Characterization》1988,5(2):51-56
This paper describes new progress obtained with an optical technique called V.I.D.E. (Visible Infra-red Double Extinction) which simultaneously measures mean particle size in the range of 10–120 μm and mean number density in densely laden media (up to 0.1% volume fraction). The underlying theory, taking account of multiple light scattering, is recalled. Simultaneous size and concentration measurements are obtained by simultaneously recording transmittances of the medium at two well chosen wavelengths. Experimental results for suspensions of glass particles in air, are described and discussed. The size of particles given by the technique agrees with that given by optical microscopy and Malvern diffractometry. The V.I.D.E. technique is shown to be very suitable to investigate dense media whose optical thickness is up to nine and for which other techniques fail. 相似文献