全文获取类型
收费全文 | 167篇 |
免费 | 2篇 |
国内免费 | 3篇 |
专业分类
化学 | 94篇 |
晶体学 | 3篇 |
力学 | 8篇 |
数学 | 43篇 |
物理学 | 24篇 |
出版年
2023年 | 2篇 |
2022年 | 5篇 |
2021年 | 4篇 |
2020年 | 6篇 |
2019年 | 12篇 |
2018年 | 7篇 |
2017年 | 4篇 |
2016年 | 5篇 |
2015年 | 1篇 |
2014年 | 5篇 |
2013年 | 10篇 |
2012年 | 12篇 |
2011年 | 16篇 |
2010年 | 6篇 |
2009年 | 6篇 |
2008年 | 7篇 |
2007年 | 8篇 |
2006年 | 8篇 |
2005年 | 6篇 |
2004年 | 4篇 |
2003年 | 10篇 |
2002年 | 6篇 |
2001年 | 4篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1998年 | 4篇 |
1997年 | 2篇 |
1996年 | 2篇 |
1995年 | 1篇 |
1994年 | 1篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 1篇 |
排序方式: 共有172条查询结果,搜索用时 15 毫秒
11.
Nawel Cheikh Didier Villemin Nathalie Bar Jean-François Lohier Nourredine Choukchou-Braham Bachir Mostefa-Kara Jana Sopkova 《Tetrahedron》2013,69(3):1234-1247
In the course of our studies on Cerpegin analogues synthesis, a serendipitous reactivity of enaminolactone nitrile has been observed. Instead of expecting iminocerpegins, we have gained new class of substituted 2-aminopyridines. The methodology has been applied on a wide range of primary amines, as aliphatic, aromatic, heteroaromatic and also, diamines, hydrazines and chiral amines. 相似文献
12.
Belmesnaoui Aqzzouz Redouane Nouira Larbi Zraoula 《Rendiconti del Circolo Matematico di Palermo》2008,57(2):287-294
We give some sufficient and necessary conditions for that a positive Dunford-Pettis operator admits a dual operator which
is also Dunford-Pettis, and conversely.
相似文献
13.
We establish some sufficient and necessary conditions which give the compactness of positive Dunford–Pettis operators on Banach lattices. To cite this article: B. Aqzzouz et al., C. R. Acad. Sci. Paris, Ser. I 340 (2005). 相似文献
14.
Grégoire Fourrié Laurent Keirsbulck Larbi Labraga Patrick Gilliéron 《Experiments in fluids》2011,50(2):385-395
A passive flow control on a generic car model was experimentally studied. This control consists of a deflector placed on the
upper edge of the model rear window. The study was carried out in a wind tunnel at Reynolds numbers based on the model height
of 3.1 × 105 and 7.7 × 105. The flow was investigated via standard and stereoscopic particle image velocimetry, Kiel pressure probes and surface flow
visualization. The aerodynamic drag was measured using an external balance and calculated using a wake survey method. Drag
reductions up to 9% were obtained depending on the deflector angle. The deflector increases the separated region on the rear
window. The results show that when this separated region is wide enough, it disrupts the development of the counter-rotating
longitudinal vortices appearing on the lateral edges of the rear window. The current study suggests that flow control on such
geometries should consider all the flow structures that contribute to the model wake flow. 相似文献
15.
Stability analysis of jointed rock slope 总被引:2,自引:0,他引:2
The stability analysis of a jointed rock slope with two sets of unfilled joints, under its own weight, is carried out directly by considering failure surfaces along some particular joints and also going through the intact rock. Simple failure mechanisms using uniform rigid rock-block motions are incorporated in the yield design kinematic approach. They yield an improvement of known results as long as the characteristics strength of the joints are weak enough. 相似文献
16.
Mohammed Larbi Labbi 《Mathematische Nachrichten》2015,288(4):402-411
The Weitzenböck curvature operators are the curvature terms of order zero that appear in the well‐known classical Weitzenböck formula. In this paper, we use the formalism of double forms to prove a simple formula for these operators and to study their geometric properties. 相似文献
17.
The geometric and electronic structures of a series of hypothetical compounds of the types CpM(C13H9N) and (CO)3M(C13H9N) (M = first row transition metal and C13H9N = 7,8-benzoquinoline) have been investigated by means of density functional theory (DFT). The benzoquinoline ligand can bind to the metal through η1-η6 coordination modes, adopting structures of types a, b and c, in agreement with the electron count and the nature of the metal. In the investigated species, the most favored closed-shell count is 18-MVE, except for the Ti and V models which prefer the open-shell 16-MVE configuration. This study has shown the difference in the coordination ability of this heteropolycyclic ligand and coordination of the inner C6 ring is less favored than the outer C6 and C5N rings, in agreement with the π-electron density localization. 相似文献
18.
Naima Bouyahia Mohamed Larbi Hamlaoui Mouna Hnaien Florence Lagarde Nicole Jaffrezic-Renault 《Bioelectrochemistry (Amsterdam, Netherlands)》2011,80(2):155-161
In this work, a new biosensor was prepared through immobilization of bovine liver catalase in a photoreticulated poly (vinyl alcohol) membrane at the surface of a conductometric transducer. This biosensor was used to study the kinetics of catalase–H202 reaction and its inhibition by cyanide. Immobilized catalase exhibited a Michaelis–Menten behaviour at low H202 concentrations (< 100 mM) with apparent constant KMapp = 84 ± 3 mM and maximal initial velocity VMapp = 13.4 μS min? 1. Inhibition by cyanide was found to be non-competitive and inhibition binding constant Ki was 13.9 ± 0.3 μM. The decrease of the biosensor response by increasing cyanide concentration was linear up to 50 μM, with a cyanide detection limit of 6 μM. In parallel, electrochemical characteristics of the catalase/PVA biomembrane and its interaction with cyanide were studied by cyclic voltammetry and impedance spectroscopy. Addition of the biomembrane onto the gold electrodes induced a significant increase of the interfacial polarization resistance RP. On the contrary, cyanide binding resulted in a decrease of Rp proportional to KCN concentration in the 4 to 50 μM range. Inhibition coefficient I50 calculated by this powerful label-free and substrate-free technique (24.3 μM) was in good agreement with that determined from the substrate-dependent conductometric biosensor (24.9 μM). 相似文献
19.
Regueiro-Figueroa M Bensenane B Ruscsák E Esteban-Gómez D Charbonnière LJ Tircsó G Tóth I de Blas A Rodríguez-Blas T Platas-Iglesias C 《Inorganic chemistry》2011,50(9):4125-4141
In this contribution we present two ligands based on a do3a platform containing a picolinate group attached to the fourth nitrogen atom of the cyclen unit, which are designed for stable lanthanide complexation in aqueous solutions. Potentiometric measurements reveal that the thermodynamic stability of the complexes is very high (log K = 21.2-23.5), being comparable to that of the dota analogues. Luminescence lifetime measurements performed on solutions of the Eu(III) and Tb(III) complexes indicate that the complexes are nine coordinate with no inner-sphere water molecules. A combination of density functional theory (DFT) calculations and NMR measurements shows that for the complexes of the heaviest lanthanides there is a major isomer in solution consisting of the enantiomeric pair Λ(δδδδ) and Δ(λλλλ), which provides square antiprismatic coordination (SAP) around the metal ion. Analysis of the Yb(III)-induced paramagnetic shifts unambiguously confirms that these complexes have SAP coordination in aqueous solution. For the light lanthanide ions however both the SAP and twisted-square antiprismatic (TSAP) isomers are present in solution. Inversion of the cyclen ring appears to be the rate-determining step for the Λ(δδδδ) ? Δ(λλλλ) enantiomerization process observed in the Lu(III) complexes. The energy barriers obtained from NMR measurements for this dynamic process are in excellent agreement with those predicted by DFT calculations. The energy barriers calculated for the arm-rotation process are considerably lower than those obtained for the ring-inversion path. Kinetic studies show that replacement of an acetate arm of dota by a picolinate pendant results in a 3-fold increase in the formation rate of the corresponding Eu(III) complexes and a significant increase of the rates of acid-catalyzed dissociation of the complexes. However, these rates are 1-2 orders of magnitude lower than those of do3a analogues, which shows that the complexes reported herein are remarkably inert with respect to metal ion dissociation. 相似文献
20.
Hossini I Harrad MA Ait Ali M El Firdoussi L Karim A Valerga P Puerta MC 《Molecules (Basel, Switzerland)》2011,16(7):5886-5895
Friedel-Craft acylation at 100 °C of 2,5,9,9-tetramethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene [ar-himachalene], a sesquiterpenic hydrocarbon obtained by catalytic dehydrogenation of α-, β- and γ-himachalenes, produces a mixture of two compounds: (3,5,5,9-tetramethyl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-yl)-ethanone (2, in 69% yield), with a conserved reactant backbone, and 3, with a different skeleton, in 21% yield. The crystal structure of 3 reveals it to be 1-(8-ethyl-8-hydroperoxy-3,5,5-trimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-ethanone. In this compound O-H…O bonds form dimers. These hydrogen-bonds, in conjunction with weaker C-H…O interactions, form a more extended supramolecular arrangement in the crystal. 相似文献