全文获取类型
收费全文 | 326篇 |
免费 | 4篇 |
国内免费 | 1篇 |
专业分类
化学 | 204篇 |
力学 | 7篇 |
数学 | 41篇 |
物理学 | 79篇 |
出版年
2022年 | 3篇 |
2021年 | 2篇 |
2018年 | 2篇 |
2017年 | 2篇 |
2015年 | 3篇 |
2014年 | 10篇 |
2013年 | 13篇 |
2012年 | 12篇 |
2011年 | 23篇 |
2010年 | 18篇 |
2009年 | 14篇 |
2008年 | 12篇 |
2007年 | 16篇 |
2006年 | 16篇 |
2005年 | 12篇 |
2004年 | 15篇 |
2003年 | 8篇 |
2002年 | 13篇 |
2001年 | 6篇 |
2000年 | 2篇 |
1999年 | 6篇 |
1996年 | 5篇 |
1995年 | 3篇 |
1994年 | 5篇 |
1993年 | 3篇 |
1992年 | 1篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 4篇 |
1988年 | 3篇 |
1987年 | 3篇 |
1986年 | 1篇 |
1985年 | 9篇 |
1984年 | 6篇 |
1983年 | 4篇 |
1982年 | 8篇 |
1981年 | 12篇 |
1980年 | 3篇 |
1979年 | 7篇 |
1978年 | 3篇 |
1977年 | 5篇 |
1976年 | 7篇 |
1974年 | 4篇 |
1973年 | 5篇 |
1972年 | 1篇 |
1971年 | 2篇 |
1970年 | 1篇 |
1965年 | 1篇 |
1912年 | 4篇 |
1911年 | 1篇 |
排序方式: 共有331条查询结果,搜索用时 38 毫秒
51.
Fridgen TD Macaleese L McMahon TB Lemaire J Maitre P 《Physical chemistry chemical physics : PCCP》2006,8(8):955-966
The infrared multiphoton dissociation (IRMPD) spectra of three homogenous proton-bound dimers are presented and the major features are assigned based on comparisons with the neutral alcohol and with density functional theory calculations. As well, the IRMPD spectra of protonated propanol and the propanol/water proton-bound dimer (or singly hydrated protonated propanol) are presented and analysed. Two primary IRMPD photoproducts were observed for each of the alcohol proton bound dimers and were found to vary with the frequency of the radiation impinging upon the ions. For example, when the proton-bound dimer absorbs weakly a larger amount of S(N)2 product, protonated ether and water, are observed. When the proton-bound dimer absorbs more strongly, an increase in the simple dissociation product, protonated alcohol and neutral alcohol, is observed. With the aid of RRKM calculations this frequency dependence of the branching ratio is explained by assuming that photon absorption is faster than dissociation for these species and that only a few photons extra are necessary to make the higher-energy dissociation channel (simple cleavage) competitive with the lower energy (S(N)2) reaction channel. 相似文献
52.
Yi Lin Antoine Leydier Estelle Métay Alain Favre-Réguillon Denis Bouchu Stéphane Pellet-Rostaing Marc Lemaire 《Journal of inclusion phenomena and macrocyclic chemistry》2008,61(1-2):187-193
Calixarenes 5–8 capped with DTPA bridges were synthesized by condensation of the corresponding 1,3-(distal)-diaminocalixarenes and DTPA dianhydride in DMF. The chelating properties of the DTPA-calixarenes were evaluated towards europium and the resulting complexes were characterized by mass spectroscopy. 相似文献
53.
Frison G van der Rest G Turecek F Besson T Lemaire J Maître P Chamot-Rooke J 《Journal of the American Chemical Society》2008,130(45):14916-14917
In this study, we propose the first spectroscopic structural characterization of c-type ions produced by ECD of a peptide. The structure of c-type ions formed by electron capture dissociation and the overall mechanism leading to their formation are still a question of debate. Depending on the mechanism, c-type ions have been proposed to have either an enol-imine structure (-C(OH)NH) or an amide one (-C(O)-NH2). Since these ions are isomeric, mass spectrometry only cannot discriminate between them, but infrared spectroscopy can bring experimental evidence and help determine which scheme is operative. Using the coupling between a tunable free electron laser and a FT-ICR mass spectrometer, we show that c-type ions have an amide structure, characterized by an IR signature of the C=O stretch at 1731 cm(-1). This result is particularly interesting from the perspective of the elucidation of the ECD mechanism. 相似文献
54.
A bicyclic tetraazatriacetic chelating agent containing a thioalkyl pendant group was prepared. Four synthetic routes have been investigated via a Mitsunobu reaction from 2,4-[bishydroxymethyl]-3-hydroxy-pyridine 1. Deprotection of trityl thioether compound 5c led to ligand 6c in 22% overall yield from the starting 3-hydroxypyridine. 相似文献
55.
Miarintsoa Michaele Ranarijaona Ny Aina Harivony Rambala Rakotomena Mbolatiana Tovo Andrianjafy Fenia Diane Ramiharimanana Lydia Clarisse Herinirina Niry Hasinandrianina Ramarosandratana Benoit Briou Pauline Fajardie Patrick Mavingui Estelle Mtay Voahangy Vestalys Ramanandraibe Marc Lemaire 《Molecules (Basel, Switzerland)》2021,26(24)
This article describes a part of the results obtained from the cooperation between the University of Lyon1 (France) and the University of Antananarivo (Madagascar). It shows (among others) that useful research can be carried out in developing countries of the tropics if their social, technical, and economic conditions are taken into account. The concepts and methods associated with so-called “green chemistry” are particularly appropriated for this purpose. To illustrate this approach, two examples are shown. The first deals with industrial ecology and concerns waste transformation from the production of cashew nut into an amphiphilic product, oxyacetic derivatives. This product was obtained with a high yield and in a single step reaction. It exhibited an important surfactant property similar to those of the main fossil-based ones but with a much lower ecological impact. The second talks about chemical ecology as an alternative to insecticides and used to control dangerous mosquito populations. New substituted chromones were synthesized and showed biological activities toward Aedes albopictus mosquito species. Strong repellent properties were recorded for some alkoxylated products if others had a significant attractant effect (Kairomone) depending on their stereochemistry and the length of the alkyl chain. 相似文献
56.
Barbara Chiavarino Dr. Maria Elisa Crestoni Prof. Simonetta Fornarini Prof. Francesco Lanucara Dr. Joel Lemaire Dr. Philippe Maître Prof. Debora Scuderi Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(33):8185-8195
Anion–π interactions between a π‐acidic aromatic system and an anion are gaining increasing recognition in chemistry and biology. Herein, the binding features of an electron‐deficient aromatic system (1,3,5‐trinitrobenzene (TNB)) and selected anions (OH?, Br?, and I?) are examined in the gas phase by using the combined information derived from collision‐induced dissociation experiments at variable energy, infrared multiple‐photon dissociation spectroscopy, and quantum chemical calculations. We provide spectroscopic evidence for two different structural motifs of anion–arene complexes depending on the nature of the anion. The TNB–OR? complexes (R=H, or alkyl groups which were studied earlier) adopt an anionic σ‐complex structure whereby RO? attacks the aromatic ring with covalent bond formation, and develops a tetrahedral ring carbon bound to H and OR. The halide complexes rather conform to a structure in which the TNB moiety is hardly altered, and the halogen is placed on an unsubstituted carbon atom over the periphery of the ring at a C–X distance that is appreciably longer than a typical covalent bond length. The ensuing structural motif, previously characterized in the solid state and named weak σ interaction, is now confirmed by an IR spectroscopic assay in the gas phase, in which the sampled species are unperturbed by crystal packing or solvation effects. 相似文献
57.
Koivisto BD Ichimura AS McDonald R Lemaire MT Thompson LK Hicks RG 《Journal of the American Chemical Society》2006,128(3):690-691
The solid state structure of 1,1'-bis(verdazyl)ferrocene reveals the two radical moieties associated intramolecularly to give the first example of a pi-dimer of a stable verdazyl radical. The pi-dimer structure is not maintained in solution. Magnetic characterization indicates that the radicals are sufficiently strongly antiferromagnetically coupled so as to render the molecule diamagnetic at room temperature. 相似文献
58.
Franconi F Chapon C Lemaire L Lehmann V Barantin L Akoka S 《Magnetic resonance imaging》2002,20(8):587-592
To measure MR renograms, cortical and medullary kidney signal intensity evolution is followed after contrast agent injection. To obtain an accurate quantitative signal measurement, the use of a reference signal is necessary to correct the potential MRI system variations in time. The ERETIC method (Electronic Reference To access In vivo Concentrations) provides an electronic reference signal. It is synthesized as an amplitude modulated RF pulse applied during the acquisition. The ERETIC method was as precise as the external tube reference method but presents major advantages like its free adjustability (shape, location and magnitude) to the characteristics of the organ studied as well as its not taking room inside the magnet. Even though ERETIC showed a very good intrinsic stability, systems' variations still affect its signal in the same way as real NMR signals are affected. This method can be easily implemented on any imaging system with two RF channels. 相似文献
59.
Antoine Leydier Yi Lin Guilhem Arrachart Raphaël Turgis Delphine Lecerclé Alain Favre-Reguillon Frédéric Taran Marc Lemaire Stéphane Pellet-Rostaing 《Tetrahedron》2012,68(4):1163-1170
Synthesis of modified EDTA and DTPA ligands and determination of their binding affinities for the uranyl cation are described.Thanks to a screening method, based on a chromophoric complex displacement procedure, chelating properties were studied in aqueous media under various pH conditions for evaluation of their in vivo uranyl-removal efficacy. Each ligand showed a more or less pronounced affinity for uranium. Specific ligands based on EDTA or DTPA analogues containing sulfocatecholamide (CAMS) were found to exhibit a significant affinity towards uranyl ion in acidic, neutral or basic conditions. 相似文献
60.
Hugo Festjens Chevallier Gaël Renaud Franck Dion Jean-Luc Lemaire Remy 《Applied Acoustics》2012,73(11):1121-1128
The purpose of this publication is to give an overview of the actual role of multi-layered viscoelastic parts, so called “shims”, to prevent squeal noises of automotive brake systems. Since shear stress is usually used to damp thin structures in their bending modes it is commonly believed to be the largest underwent by shims. To check this assumption and considering that stresses underwent by shims cannot be measured experimentally, the authors have computed them with the help of a detailed and realistic finite element model. Contrary to what shims manufacturers say, this study exhibits the fact that shims are almost uniquely solicited in their normal direction in brake systems. Secondly, the study focuses on the added damping and stiffening induced by the viscoelastic materials. In order to take into account these materials, a realistic frequency dependent viscoelastic behavior has been integrated in the simulations. Finally, the study shows certains eigenmodes for which the viscoelastic behavior of the shims reveals instabilities that would not exist without it. It is shown that this is due to coalescence phenomenon. 相似文献