全文获取类型
收费全文 | 1435篇 |
免费 | 49篇 |
专业分类
化学 | 930篇 |
晶体学 | 4篇 |
力学 | 32篇 |
数学 | 244篇 |
物理学 | 274篇 |
出版年
2023年 | 12篇 |
2022年 | 9篇 |
2020年 | 12篇 |
2019年 | 16篇 |
2018年 | 18篇 |
2017年 | 19篇 |
2016年 | 35篇 |
2015年 | 38篇 |
2014年 | 42篇 |
2013年 | 60篇 |
2012年 | 85篇 |
2011年 | 99篇 |
2010年 | 57篇 |
2009年 | 43篇 |
2008年 | 87篇 |
2007年 | 105篇 |
2006年 | 97篇 |
2005年 | 85篇 |
2004年 | 77篇 |
2003年 | 41篇 |
2002年 | 46篇 |
2001年 | 23篇 |
2000年 | 16篇 |
1999年 | 6篇 |
1998年 | 6篇 |
1997年 | 15篇 |
1996年 | 11篇 |
1995年 | 13篇 |
1994年 | 15篇 |
1993年 | 10篇 |
1992年 | 17篇 |
1991年 | 13篇 |
1990年 | 10篇 |
1988年 | 11篇 |
1987年 | 11篇 |
1985年 | 18篇 |
1984年 | 11篇 |
1983年 | 10篇 |
1982年 | 18篇 |
1981年 | 15篇 |
1980年 | 12篇 |
1979年 | 9篇 |
1978年 | 8篇 |
1977年 | 16篇 |
1975年 | 8篇 |
1974年 | 11篇 |
1973年 | 12篇 |
1972年 | 7篇 |
1971年 | 7篇 |
1970年 | 6篇 |
排序方式: 共有1484条查询结果,搜索用时 62 毫秒
81.
Casper Jon Steenbjerg Ibsen Bjørn Fridur Mikladal Uffe Bjørnholt Jensen Assoc. Prof. Henrik Birkedal 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(49):16112-16120
Three dimensional hierarchical materials are widespread in nature but are difficult to synthesize by using self‐assembly/organization. Here, we employ a gel–liquid interface to obtain centimeter‐long ~100 μm diameter tubes with complex mineral wall structures that grow from the interface into solution. The gel, made from gelatin, is loaded with metal chloride salt, whereas the solution is a high pH anion source. Tubes were obtained with a range of cations (Ca2+, Sr2+, Ba2+, Cu2+, and Zn2+) and anions (CO32? and PO43?). The crystalline phases found in the tube walls corresponded to expectations from solution chemistries and phase solubilities. The growth mechanism is found to be akin to that of chemical gardens. The divalent cations modify the strength of the gelatin gel in a manner that involves not only simple electrostatic screening, but also ion‐specific effects. Thus, tubes were not obtained for those ions and/or concentrations that significantly changed the gel’s mechanical structure. At high Cu2+ loading, for example, vertical convection bands, not Liesegang bands, were observed in the gels. 相似文献
82.
Gerardo Algara‐Siller Dr. Nikolai Severin Samantha Y. Chong Dr. Torbjörn Björkman Dr. Robert G. Palgrave Andrea Laybourn Prof. Dr. Markus Antonietti Prof. Yaroslav Z. Khimyak Dr. Arkady V. Krasheninnikov Prof. Dr. Jürgen P. Rabe Prof. Dr. Ute Kaiser Prof. Andrew I. Cooper Prof. Dr. Arne Thomas Dr. Michael J. Bojdys 《Angewandte Chemie (International ed. in English)》2014,53(29)
83.
Björn Johansson Prof. Fredrik Höök Prof. David Klenerman Dr. Peter Jönsson 《Chemphyschem》2014,15(3):486-491
An important and characteristic property of a cell membrane is the lateral mobility of protein molecules in the lipid bilayer. This has conventionally been measured by labeling the molecules with fluorescent markers and monitoring their mobility by different fluorescence‐based techniques. However, adding the label to the studied molecule may affect the system, so it is an assumption in almost all experiments that the measured mobility of the biomolecule with its label is the same as that of the unlabeled molecule. However, this assumption is rarely tested due to a lack of suitable methods. In this work, a new technique to perform label‐free diffusivity measurements is developed and used to measure the effect of the label for two common protein–lipid systems: 1) streptavidin (SA) coupled to a supported lipid bilayer (SLB) through biotinylated lipids and 2) the extracellular part of the T‐cell adhesion protein CD2, coupled to an SLB through histidine tags to nickel‐chelating lipids. A measurable (≈12 %) decrease in diffusivity is found for both labeled proteins, even though the molecular mass of the label is almost 100 times smaller than those of the proteins (≈50 kDa). The results illustrate the importance of being able to study different biophysical properties of cell membranes and their mimics without relying on fluorescent labels, especially if fluorescent labeling is difficult or is expected to affect the nature of the intermolecular interactions being studied. 相似文献
84.
Michael Höfner Björn Kobin Prof. Dr. Stefan Hecht Prof. Dr. Fritz Henneberger 《Chemphyschem》2014,15(17):3805-3808
We investigate the coupling of ladder‐type quarterphenyl to the photon modes of a dielectric ZrOx/SiOx microcavity at ultraviolet wavelengths. For a relatively long cavity (≈10 μm) with high‐reflectivity mirrors (0.998), optically pumped laser action is demonstrated in the weak‐coupling regime. We observe single‐mode operation with a threshold of 0.4 mJ cm?2. Strong coupling is achieved by using a short λ/2 cavity. We find pronounced anti‐crossing features of the molecular (0,0) and (0,1) vibronic transitions and the cavity mode in angle‐dependent reflectivity measurements providing Rabi splittings of (90±10) meV. All these features occur spectrally resonant to the exciton transition of ZnO demonstrating the potential of ladder‐type oligo(p‐phenylene)s for the construction of inorganic/organic hybrid microcavities. 相似文献
85.
Adsorption of Large Hydrocarbons on Coinage Metals: A van der Waals Density Functional Study
下载免费PDF全文
![点击此处可从《Chemphyschem》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The adsorption of organic molecules onto the close‐packed facets of coinage metals is studied, and how accurately adsorption heights can be described by using recent advances of the van der Waals density functional (vdWDF), with optPBE/vdWDF, optB86b/vdWDF, vdWDF2, and rev/vdWDF2 functionals is illustrated. The adsorption of two prototypical aromatic hydrocarbons is investigated, and the calculated adsorption heights are compared to experimental literature values from normal incident X‐ray standing wave absorption and a state‐of‐the‐art semi‐empirical method. It is shown that both the optB86b/vdWDF and rev/vdWDF2 functionals describe adsorption heights with an accuracy of 0.1 Å, compared to experimental values, and are concluded as reliable methods of choice for related systems. 相似文献
86.
We present a higher-order cut cell immersed boundary method (IBM) for the simulation of high Mach number flows. As a novelty on a cut cell grid, we evaluate an adaptive local time stepping (LTS) scheme in combination with an artificial viscosity–based shock-capturing approach. The cut cell grid is optimized by a nonintrusive cell agglomeration strategy in order to avoid problems with small or ill-shaped cut cells. Our approach is based on a discontinuous Galerkin discretization of the compressible Euler equations, where the immersed boundary is implicitly defined by the zero isocontour of a level set function. In flow configurations with high Mach numbers, a numerical shock-capturing mechanism is crucial in order to prevent unphysical oscillations of the polynomial approximation in the vicinity of shocks. We achieve this by means of a viscous smoothing where the artificial viscosity follows from a modal decay sensor that has been adapted to the IBM. The problem of the severe time step restriction caused by the additional second-order diffusive term and small nonagglomerated cut cells is addressed by using an adaptive LTS algorithm. The robustness, stability, and accuracy of our approach are verified for several common test cases. Moreover, the results show that our approach lowers the computational costs drastically, especially for unsteady IBM problems with complex geometries. 相似文献
87.
88.
89.
Erik Allard Rikard Åslund Tröger Björn Arvidsson Per Johan Ragnar Sjöberg 《Rapid communications in mass spectrometry : RCM》2010,24(4):429-435
Precision, reproducibility and lower limit of quantitation (LLOQ) are important characteristics of a quantitative method. We have investigated these properties for Ximelagatran (Xi), which has a high tendency to form doubly charged ions in electrospray ionization (ESI), by studying the percentage of doubly charged species formed when varying the formic acid (FA) concentration, analyte concentration, amount of organic modifier and flow rate. It was found that the percentage of [Xi + 2H]2+ can be controlled to be more than 90% or less than 10% by varying the amount of FA present, and that the change between these values is dramatic. Furthermore, the percentage of [Xi + 2H]2+ formed decreases with increased analyte concentration and increased flow rate. No apparent relationship with the amount of organic modifier was found. The results have the implication that, by carefully controlling the selected parameters, the LLOQ, precision and reproducibility can be improved. We have compared the fragmentation of the singly and doubly charged species and concluded that the [Xi + 2H]2+ ion is more inclined to undergo fragmentation than [Xi + H]+. As a consequence, unusual instrumental settings had to be used for the experiments. The fragmentation patterns are to a great extent similar, but the doubly charged species is more inclined to generate low‐mass product ions. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
90.
Estephania Lira Jonas ?. Hansen Peipei Huo Ralf Bechstein Patrick Galliker Erik L?gsgaard Bj?rk Hammer Stefan Wendt Flemming Besenbacher 《Surface science》2010,604(21-22):1945-1960
High-resolution scanning tunneling microscopy (STM) and temperature-programmed desorption (TPD) were used to study the interaction of O2 with reduced TiO2(110)–(1 × 1) crystals. STM is the technique of choice to unravel the relation between vacancy and non-vacancy assisted O2 dissociation channels as a function of temperature. It is revealed that the vacancy-assisted, first O2 dissociation channel is preferred at low temperature (~ 120 K), whereas the non-vacancy assisted, second O2 dissociation channel operates at temperatures higher than 150 K–180 K. Based on the STM results on the two dissociative O2 interaction channels and the TPD data, a new comprehensive model of the O2 chemisorption on reduced TiO2(110) is proposed. The model explains the relations between the two dissociative and the molecular O2 interaction channels. The experimental data are interpreted by considering the available charge in the near-surface region of reduced TiO2(110) crystals, the kinetics of the two O2 dissociation channels as well as the kinetics of the diffusion and reaction of Ti interstitials. 相似文献