全文获取类型
收费全文 | 1053篇 |
免费 | 79篇 |
国内免费 | 5篇 |
专业分类
化学 | 797篇 |
晶体学 | 3篇 |
力学 | 17篇 |
数学 | 182篇 |
物理学 | 138篇 |
出版年
2024年 | 4篇 |
2023年 | 23篇 |
2022年 | 36篇 |
2021年 | 47篇 |
2020年 | 65篇 |
2019年 | 68篇 |
2018年 | 24篇 |
2017年 | 22篇 |
2016年 | 59篇 |
2015年 | 60篇 |
2014年 | 46篇 |
2013年 | 60篇 |
2012年 | 71篇 |
2011年 | 83篇 |
2010年 | 57篇 |
2009年 | 68篇 |
2008年 | 65篇 |
2007年 | 55篇 |
2006年 | 41篇 |
2005年 | 40篇 |
2004年 | 28篇 |
2003年 | 23篇 |
2002年 | 15篇 |
2001年 | 6篇 |
2000年 | 5篇 |
1999年 | 6篇 |
1997年 | 5篇 |
1995年 | 3篇 |
1994年 | 2篇 |
1993年 | 2篇 |
1992年 | 4篇 |
1991年 | 4篇 |
1990年 | 3篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1986年 | 4篇 |
1985年 | 3篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1978年 | 3篇 |
1977年 | 3篇 |
1976年 | 3篇 |
1974年 | 1篇 |
1972年 | 1篇 |
1968年 | 2篇 |
1967年 | 1篇 |
1966年 | 1篇 |
1964年 | 1篇 |
排序方式: 共有1137条查询结果,搜索用时 0 毫秒
61.
62.
63.
The highly enantiomerically enriched silyllithium compound lithiomethylphenyl(1-piperidinylmethyl)silane (4) reacts stereospecifically with chlorosilanes, but over a period of several hours slow racemization in solution at room temperature occurs, which can be suppressed by a transmetalation reaction with MgBr2(thf)4. 相似文献
64.
65.
Coherent anti-Stokes Raman spectra of the Q-branches of N2, O2 and of v1 of C2H2 have been measured with fairly high resolution (≈ 0.30 cm-1) by means of a pulsed dye laser system. Calculated CARS spectra show very good agreement with the observed rotational Q-branch structure. 相似文献
66.
Schreiner E Nicolini C Ludolph B Ravindra R Otte N Kohlmeyer A Rousseau R Winter R Marx D 《Physical review letters》2004,92(14):148101
The temperature-dependent behavior of a solvated oligopeptide, GVG(VPGVG), is investigated. Spectroscopic measurements, thermodynamic measurements, and molecular dynamics simulations find that this elastinlike octapeptide behaves as a two-state system that undergoes an "inverse temperature" folding transition and reentrant unfolding close to the boiling point of water. A molecular picture of these processes is presented, emphasizing changes in the dynamics of hydrogen bonding at the protein/water interface and peptide backbone librational entropy. 相似文献
67.
The mechanism of specific acid-catalyzed glycosidic bond formation between methanol and alpha-d-glucopyranoside in aqueous solution at 300 K was studied using Car-Parrinello molecular dynamics. The reaction was found to proceed through a non-solvent equilibrated oxocarbenium cation intermediate characterized by the loss of a hydrogen-bonding interaction between the ring oxygen and solvating water. The mechanism, which was found to be D(N)A(N) in nature, is discussed in detail. 相似文献
68.
69.
Robert Cichon Dominik Raab Simon Hewera Andrea Lazik-Palm Jens Theysohn Stefan Landgraeber Wojciech Kowalczyk 《PAMM》2016,16(1):77-78
In recent years, femoroacetabular impingement (FAI) has become increasingly common. As published in the literature, FAI is caused by an unphysiological contact between the proximal femur and the acetabular rim, which may lead to pain, limitation of movement, and damage of cartilage. In this paper, patient-specific finite element simulations of the movement of the hip based on gait motion data and MRI segmentation were conducted to check stresses of the acetabulum and femur, and additionally whether a bony contact is present or not. The study's findings show no bony contact between femur and acetabulum, which may lead to the hypothesis that the labrum and its deformation and/or the articular capsule are involved in the mechanism of FAI. In order to verify this hypothesis more simulations including labrum and capsule must be performed. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
70.
Dr. Carsten Lenczyk Dr. Dipak Kumar Roy Kai Oberdorf Dr. Jörn Nitsch Dr. Rian D. Dewhurst Dr. Krzysztof Radacki Prof. Dr. Jean-François Halet Prof. Dr. Todd B. Marder Prof. Dr. Matthias Bickelhaupt Prof. Dr. Holger Braunschweig 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(72):16544-16549
The reactivity of a diruthenium tetrahydride complex towards three selected dihydroboranes was investigated. The use of [DurBH2] (Dur=2,3,5,6-Me4C6H) and [(Me3Si)2NBH2] led to the formation of bridging borylene complexes of the form [(Cp*RuH)2BR] (Cp*=C5Me5; 1 a : R=Dur; 1 b : R=N(SiMe3)2) through oxidative addition of the B−H bonds with concomitant hydrogen liberation. Employing the more electron-deficient dihydroborane [3,5-(CF3)2-C6H3BH2] led to the formation of an anionic complex bearing a tetraarylated chain of four boron atoms, namely Li(THF)4[(Cp*Ru)2B4H5(3,5-(CF3)2C6H3)4] ( 4 ), through an unusual, incomplete threefold dehydrocoupling process. A comparative theoretical investigation of the bonding in a simplified model of 4 and the analogous complex nido-[1,2(Cp*Ru)2(μ-H)B4H9] ( I ) indicates that there appear to be no classical σ-bonds between the boron atoms in complex I , whereas in the case of 4 the B4 chain better resembles a network of three B−B σ bonds, the central bond being significantly weaker than the other two. 相似文献