全文获取类型
收费全文 | 95篇 |
免费 | 4篇 |
专业分类
化学 | 44篇 |
力学 | 9篇 |
数学 | 5篇 |
物理学 | 41篇 |
出版年
2023年 | 2篇 |
2022年 | 1篇 |
2020年 | 1篇 |
2019年 | 2篇 |
2018年 | 4篇 |
2016年 | 11篇 |
2014年 | 2篇 |
2013年 | 1篇 |
2012年 | 3篇 |
2011年 | 3篇 |
2010年 | 3篇 |
2009年 | 4篇 |
2008年 | 5篇 |
2007年 | 5篇 |
2006年 | 3篇 |
2005年 | 1篇 |
2004年 | 2篇 |
2003年 | 2篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 9篇 |
1998年 | 1篇 |
1996年 | 1篇 |
1995年 | 3篇 |
1994年 | 5篇 |
1993年 | 4篇 |
1991年 | 1篇 |
1989年 | 1篇 |
1988年 | 1篇 |
1984年 | 4篇 |
1983年 | 1篇 |
1980年 | 1篇 |
1978年 | 2篇 |
1976年 | 2篇 |
1975年 | 2篇 |
1974年 | 1篇 |
1973年 | 2篇 |
排序方式: 共有99条查询结果,搜索用时 281 毫秒
91.
92.
93.
Mounir Laroussi J. Reece Roth 《International Journal of Infrared and Millimeter Waves》1993,14(8):1601-1617
In monostatic radar applications it is the signal back to the source that is responsible for target detection. The back-scattering cross-section allows one to calculate the amount of power reflected back in the direction of incidence. In this paper, we develop theoretically and calculate computationally the back-scattering cross-section of a cylindrical column of magnetized plasma with a uniform number density. The effect of the plasma number density and of the collision frequency are investigated. 相似文献
94.
95.
Guan B Ciampi S Le Saux G Gaus K Reece PJ Gooding JJ 《Langmuir : the ACS journal of surfaces and colloids》2011,27(1):328-334
We report the use of copper(I)-catalyzed alkyne-azide cycloaddition reaction (CuAAC) to selectively functionalize the internal and external surfaces of mesoporous materials. Porous silicon rugate filters with narrow line width reflectivity peaks were employed to demonstrate this selective surface functionalization approach. Hydrosilylation of a dialkyne species, 1,8-nonadiyne, was performed to stabilize the freshly fabricated porous silicon rugate filters against oxidation and to allow for further chemical derivatization via "click" CuAAC reactions. The external surface was modified through CuAAC reactions performed in the absence of nitrogen-based Cu(I)-stabilizing species (i.e., ligand-free reactions). To subsequently modify the interior pore surface, stabilization of the Cu(I) catalyst was required. Optical reflectivity measurements, water contact angle measurements, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) were used to demonstrate the ability of the derivatization approach to selectively modify mesoporous materials with different surface chemistry on the exterior and interior surfaces. Furthermore, porous silicon rugate filters modified externally with the cell-adhesive peptide Gly-Arg-Gly-Asp-Ser (GRGDS) allowed for cell adhesion via formation of focal adhesion points. Results presented here demonstrate a general approach to selectively modify mesoporous silicon samples with potential applications for cell-based biosensing. 相似文献
96.
Ditte L. Thomsen Charles M. Nichols Jennifer N. Reece Steen Hammerum Veronica M. Bierbaum 《Journal of the American Society for Mass Spectrometry》2014,25(2):159-168
The enhanced reactivity of α-nucleophiles, which contain an electron lone pair adjacent to the reactive site, has been demonstrated in solution and in the gas phase and, recently, for the gas-phase SN2 reactions of the microsolvated HOO–(H2O) ion with methyl chloride. In the present work, we continue to explore the significance of microsolvation on the α-effect as we compare the gas-phase reactivity of the microsolvated α-nucleophile HOO–(H2O) with that of microsolvated normal alkoxy nucleophiles, RO–(H2O), in reactions with methyl formate, where three competing reactions are possible. The results reveal enhanced reactivity of HOO–(H2O) towards methyl formate, and clearly demonstrate the presence of an overall α-effect for the reactions of the microsolvated α-nucleophile. The association of the nucleophiles with a single water molecule significantly lowers the degree of proton abstraction and increases the SN2 and BAC2 reactivity compared with the unsolvated analogs. HOO–(H2O) reacts with methyl formate exclusively via the BAC2 channel. While microsolvation lowers the overall reaction efficiency, it enhances the BAC2 reaction efficiency for all anions compared with the unsolvated analogs. This may be explained by participation of the solvent water molecule in the BAC2 reaction in a way that continuously stabilizes the negative charge throughout the reaction.
Figure 相似文献
97.
Umar Rashid Elarbi Chatir Leonardo Medrano Sandonas PA Sreelakshmi Arezoo Dianat Rafael Gutierrez Gianaurelio Cuniberti Saioa Cobo Veerabhadrarao Kaliginedi 《Angewandte Chemie (International ed. in English)》2023,62(16):e202218767
By employing a mechanically controllable break junction technique, we have realized an ideal single molecular linear actuator based on dithienylethene (DTE) based molecular architecture, which undergoes reversible photothermal isomerization when subjected to UV irradiation under ambient conditions. As a result, open form (compressed, UV OFF) and closed form (elongated, UV ON) of dithienylethene-based molecular junctions are achieved. Interestingly, the mechanical actuation is achieved without changing the conductance of the molecular junction around the Fermi level over several cycles, which is an essential property required for an ideal single molecular actuator. Our study demonstrates a unique example of achieving a perfect balance between tunneling width and barrier height change upon photothermal isomerization, resulting in no change in conductance but a change in the molecular length, which results in mechanical actuation at the single molecular level. 相似文献
98.
Hayley A. Reece Demetrius C. Levendis 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(3):o105-o108
Gabapentin [or 1‐(aminomethyl)cyclohexaneacetic acid], C9H17NO2, exists as a zwitterion [1‐(ammoniomethyl)cyclohexaneacetate] in the solid state. The crystal structures and bonding networks of two new monoclinic polymorphs (β‐gabapentin and γ‐gabapentin) are studied and compared with a previously reported gabapentin polymorph [α‐gabapentin: Ibers (2001). Acta Cryst. C 57 , 641–643]. All three polymorphs have extensive networks of hydrogen bonds between the NH3+ and COO− groups of neighbouring molecules. In β‐gabapentin, there is an additional weak intramolecular hydrogen bond. 相似文献
99.
Jankiewicz BJ Gao J Reece JN Vinueza NR Narra P Nash JJ Kenttämaa HI 《The journal of physical chemistry. A》2012,116(12):3089-3093
Recent studies have shown that the reactivity of the 4-dehydropyridinium cation significantly differs from the reactivities of its isomers toward tetrahydrofuran. While only hydrogen atom abstraction was observed for the 2- and 3-dehydropyridinium cations, nonradical reactions were observed for the 4-isomer. In order to learn more about these reactions, the gas-phase reactivities of the 4-dehydropyridinium cation and several of its derivatives toward tetrahydrofuran were investigated in a Fourier transform ion electron resonance mass spectrometer. Both radical and nonradical reactions were observed for most of these positively charged radicals. The major parameter determining whether nonradical reactions occur was found to be the electron affinity of the radicals--only those with relatively high electron affinities underwent nonradical reactions. The reactivities of the monoradicals are also affected by hydrogen bonding and steric effects. 相似文献