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排序方式: 共有143条查询结果,搜索用时 531 毫秒
41.
D.B. Bastien M.F. Hodous R.I. Hulsizer A. Napier I.A. Pless J.P. Silverman J. Wolfson P.L. Bastien L.D. Kirkpatrick H.J. Lubatti 《Physics letters. [Part B]》1974,50(2):290-294
We have investigated the interaction at 5.1 GeV/c using the prism plot method. In addition to the final state, we isolate the three particle diffractive dissociation of the proton and antiproton into (pπ+π?) and respectively. We estimate this process accounts for 30% of the final state. 相似文献
42.
Roland Coratger Bastien Calmettes Youness Benjalal Xavier Bouju Christophe Coudret 《Surface science》2012,606(3-4):444-449
The electronic and structural properties of large molecules composed of a central hexa-phenylbenzene core surrounded by six adamantyl groups (Ad6HPB) adsorbed on Ag(111) have been investigated using low temperature scanning tunneling microscopy (STM), adsorption and image calculations. On large 2D domains, the molecular organization displays two lattices. In one of them, molecules are slightly nested as a result of their relative flexibility during packing. These compounds also exhibit contrast variations in terms of used bias voltage in the self-assembled domains as well as in single molecule observations. This is attributed to the peculiar electronic properties of Ad6HPB and to the role of peripheral groups. 相似文献
43.
44.
Cover Picture: Theoretical and Experimental Study on Boron β‐Diketonate Complexes with Intense Two‐Photon‐Induced Fluorescence in Solution and in the Solid State (ChemPhysChem 14/2016) 下载免费PDF全文
45.
Harnessing the Lewis Acidity of HFIP through its Cooperation with a Calcium(II) Salt: Application to the Aza‐Piancatelli Reaction 下载免费PDF全文
Dr. David Lebœuf Lucile Marin Bastien Michelet Dr. Alejandro Perez‐Luna Régis Guillot Dr. Emmanuelle Schulz Prof. Vincent Gandon 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(45):16165-16171
A method to extend the scope of the aza‐Piancatelli reaction between 2‐furylcarbinols and anilines is depicted. We found that 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP) is the solvent of choice for this transformation, as it outcompetes the usual solvents in terms of rate and yield. Side reactions and other issues raised by the title reaction are prevented, thereby providing an avenue to complex molecules that were previously inaccessible. Lewis acidity studies and computations were carried out to unveil the role of HFIP. Based on these results, we propose that HFIP is, in fact, acting as a Lewis acid and that its acidity can be enhanced when combined with a calcium(II) salt. 相似文献
46.
Dr. Bastien Chatelet Dr. Lionel Joucla Dr. Jean‐Pierre Dutasta Dr. Alexandre Martinez Dr. Véronique Dufaud 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(28):8571-8574
The endohedral functionalization of a molecular cage by an azaphosphatrane unit has allowed for the creation of highly engineered catalytic cavities for efficient conversion of CO 2 into cyclic carbonates. Strong structure/activity/stability correlations have been demonstrated by careful adjustment of the size, shape, and electronic properties of the hemicryptophane host. 相似文献
47.
Bastien Néel Majid Ghahraman Asfhar Gastón A. Crespo Marcin Pawlak Denis Dorokhin Eric Bakker 《Electroanalysis》2014,26(3):473-480
A series of polymeric nitrite‐selective electrodes containing a new lipophilic ionophore Co(II) tert‐butyl‐salophen is reported. The stability of Co(II) ionophores within a PVC‐based membrane was investigated by leaching experiments. Different membrane compositions were explored in order to reach the lowest possible limit of detection for a PVC‐based nitrite selective polymeric membrane electrode containing this ionophore. The optimal electrode showed a limit of detection of 2×10?6 M and exhibited four orders of magnitude of discrimination over nitrate, chloride and bromide. The electrodes were evaluated in undiluted human urine and attest to the robustness of the ionophore. 相似文献
48.
We consider the (traveling-wave-like) fronts which propagate with rational velocityp/q in a simple coupled map lattice for which the local map has two stable fixed points. We prove the uniqueness of such orbits up to time iterations, space translations, and permutations of the associated codes. A condition for their existence is also given, but it has to be checked in each case. We expect this condition to serve as a selection mechanism. The technique employed, the so-called (generalized) transfer matrix method, allows us to give explicit expressions for these solutions. These fronts are actually the observed orbits in the numerical simulations, as is shown with two examples: the case of velocity 1/2 and that of velocity 1. 相似文献
49.
Bastien Fernandez David Gérard-Varet Giambattista Giacomin 《Annales Henri Poincare》2016,17(7):1793-1823
We consider the Kuramoto model of globally coupled phase oscillators in its continuum limit, with individual frequencies drawn from a distribution with density of class \({C^n}\) (\({n\geq 4}\)). A criterion for linear stability of the uniform stationary state is established which, for basic examples in the literature, is equivalent to the standard condition on the coupling strength. We prove that, under this criterion, the Kuramoto order parameter, when evolved under the full nonlinear dynamics, asymptotically vanishes (with polynomial rate n) for every trajectory issued from a sufficiently small \({C^n}\) perturbation. The proof uses techniques from the Analysis of PDEs and closely follows recent proofs of the nonlinear Landau damping in the Vlasov equation and Vlasov-HMF model. 相似文献
50.
Codée JD Kröck L Castagner B Seeberger PH 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(13):3987-3994
For automated oligosaccharide synthesis to impact glycobiology, synthetic access to most carbohydrates has to become efficient and routine. Methods to install "difficult" glycosidic linkages have to be established and incorporated into the overall synthetic concept. Described here is the first automated solid-phase synthesis of oligosaccharides containing the challenging beta-mannosidic linkage. Carboxybenzyl mannoside building blocks proved effective beta-mannosylation agents and resulted in excellent conversion and good to moderate selectivities. [(Triisopropylsilyl)oxy]-methyl ether (Tom), served as an orthogonal, minimally intrusive, and readily cleavable protecting group for the elongation of the C3 position of mannose. The desired oligosaccharide products were readily separated from by-products containing unwanted stereoisomers using reverse-phase HPLC. The methods described here expand the scope of carbohydrates currently accessible by automation as many oligosaccharides of biological interest contain beta-mannosidic linkages. 相似文献