全文获取类型
收费全文 | 201篇 |
免费 | 4篇 |
国内免费 | 3篇 |
专业分类
化学 | 92篇 |
晶体学 | 1篇 |
数学 | 32篇 |
物理学 | 83篇 |
出版年
2018年 | 1篇 |
2016年 | 2篇 |
2015年 | 1篇 |
2014年 | 1篇 |
2013年 | 7篇 |
2012年 | 3篇 |
2011年 | 4篇 |
2009年 | 2篇 |
2008年 | 5篇 |
2007年 | 4篇 |
2006年 | 7篇 |
2005年 | 10篇 |
2004年 | 7篇 |
2003年 | 4篇 |
2002年 | 5篇 |
2001年 | 3篇 |
2000年 | 4篇 |
1999年 | 3篇 |
1998年 | 5篇 |
1997年 | 4篇 |
1995年 | 2篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1992年 | 1篇 |
1991年 | 2篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1988年 | 3篇 |
1987年 | 1篇 |
1986年 | 5篇 |
1985年 | 13篇 |
1984年 | 8篇 |
1983年 | 2篇 |
1982年 | 7篇 |
1981年 | 9篇 |
1980年 | 7篇 |
1979年 | 7篇 |
1978年 | 10篇 |
1977年 | 8篇 |
1976年 | 6篇 |
1975年 | 2篇 |
1974年 | 20篇 |
1973年 | 7篇 |
排序方式: 共有208条查询结果,搜索用时 31 毫秒
121.
D.S.C. Yee A. Hamnett C.E. Brion 《Journal of Electron Spectroscopy and Related Phenomena》1976,8(4):291-312
The Penning electron spectra of water, methanol, ethanol, isopropyl alcohol, tertiary butyl alcohol, dimethyl ether, ethylene oxide, diethyl ether, tetrahydrofuran and 1,4 dioxane, obtained using helium metastable atoms (21S, 23S), are compared to their respective photoelectron spectra at 584 Å. An analysis of the Penning electron band shape and the position of the peak maximum for the ground state ions suggest significant changes in the Franck—Condon factors in comparison with photoelectron spectra. This may be ascribed to modifications of the target potential energy curves. It is also observed that the relative populations of the ionic states differ appreciably for Penning ionization and photoionization. 相似文献
122.
The S 2p, S 2s and F 1s inner shell excitation spectra of SF6 have been examined by small angle, inelastic scattering of 2.5 keV electrons. While the main features of the spectra are in agreement with previous photoabsorption spectra, a number of new features have been observed. A detailed investigation of the S 2p spectrum below the ionization limit has been performed. The weak Rydberg structure in this region has been interpreted on the basis of a comparison of the present electron energy loss results with previous photoabsorption studies. Part of the Rydberg structure in the electron impact spectrum has been identified as arising from electric quadrupole transitions. 相似文献
123.
R.N.S. Sodhi S. Da Viel C.E. Brion G.G.B. De Souza 《Journal of Electron Spectroscopy and Related Phenomena》1985,35(1):45-64
Inner shell excitation spectra of tetramethylsilane, (CH3)4Si, have been measured in the silicon 2s, 2p (LI,II,III-shell) and carbon is (K-shell) regions using electron energy-loss spectroscopy at an impact energy of 2.5 keV and a scattering angle of ~1°. The high-resolution valence shell spectrum has also been observed at an impact energy of 3 keV and a zero degree scattering angle. The silicon 2p spectra are compared and contrasted with published photoabsorption spectra of SiF4, SiH4, and other related Si-containing molecules with varying ligands. 相似文献
124.
Stereoretentive Palladium‐Catalyzed Arylation,Alkenylation, and Alkynylation of 1‐Thiosugars and Thiols Using Aminobiphenyl Palladacycle Precatalyst at Room Temperature
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Alexandre Bruneau Dr. Maxime Roche Dr. Abdallah Hamze Dr. Jean‐Daniel Brion Dr. Mouad Alami Dr. Samir Messaoudi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(23):8375-8379
A general and efficient protocol for the palladium‐catalyzed functionalization of mono‐ and polyglycosyl thiols by using the palladacycle precatalyst G3‐XantPhos was developed. The C?S bond‐forming reaction was achieved rapidly at room temperature with various functionalized (hetero)aryl‐, alkenyl‐, and alkynyl halides. The functional group tolerance on the electrophilic partner is typically high and anomer selectivities of thioglycosides are high in all cases studied. New sulfur nucleophiles such as thiophenols, alkythiols, and thioaminoacids (cysteine) were also successfully coupled to lead to the most general and practical method yet reported for the functionalization of thiols. 相似文献
125.
M. Pnitsch P. Gotthardt A. Grüger H. G. Brion R. Kirchheim 《Journal of Polymer Science.Polymer Physics》1997,35(15):2397-2408
Small molecules in glassy polymers are considered to occupy sites with a distribution of free energies of dissolution. Then their diffusivity depends on concentration and temperature in the same way as it has been derived for hydrogen atoms in metallic glasses. For hydrogen it was shown that the tracer diffusion coefficient is proportional to the activity coefficient of the solute atoms. The latter can be evaluated from measured data of sorption of the small molecules in the polymer. Knowing this quantity, the thermodynamic factor can be calculated and the concentration dependence of the mutual diffusion coefficient is obtained in excellent agreement with published experimental results. New experimental results are presented for the diffusion coefficient of CO2 in Kapton and four polycarbonates (BPA-PC, BPZ-PC, TMBPA-PC, and TMC-PC) in the low CO2 pressure range of a few mbar up to 1 bar. The results are in agreement with the model developed for hydrogen. The reference diffusion coefficient, which is a fitting parameter of the model that is independent of the distribution of free energies is smallest for the polycarbonate BPZ-PC having a high γ-relaxation temperature. This correlation between the diffusion coefficient and the dynamics of the polymer can be found for other substituted polycarbonates as well. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35 : 2397–2408, 1997 相似文献
126.
Renfei Feng Glyn Cooper Gordon R. Burton C. E. Brion Lorenzo Avaldi 《Chemical physics》1999,240(3):231
Absolute photoabsorption oscillator strengths (cross-sections) for the valence shell discrete and continuum regions of sulphur dioxide from 3.5 to 51 eV have been measured using high resolution (0.05 eV FWHM) dipole (e,e) spectroscopy. A wide-range spectrum, covering both the valence shell and the S 2p and 2s inner shells, has also been obtained from 5 to 260 eV at low resolution (1 eV FWHM), and this has been used to determine the absolute oscillator strength scale using valence shell TRK (i.e., S(0)) sum-rule normalization. The present measurements have been undertaken in order to investigate the recently discovered significant quantitative errors in our previously published low resolution dipole (e,e) work on sulphur dioxide (Cooper et al., Chem. Phys. 150 (1991) 237; 150 (1991) 251). These earlier measurements were also in poor agreement with other previously published direct photoabsorption measurements. We now report new absolute photoabsorption oscillator strengths using both high and low resolution dipole (e,e) spectroscopies. These new measurements cover a wider energy range and are much more consistent with the previously published direct photoabsorption measurements. The accuracy of our new measurements is confirmed by an S(−2) dipole sum-rule analysis which gives a static dipole polarizability for sulphur dioxide in excellent agreement (within 3.5%) with previously reported polarizability values. Other dipole sums S(u) (u=−1,−3 to −6,−8,−10) and logarithmic dipole sums L(u) (u=−1 to −6) are also determined from the presently reported absolute oscillator strength distributions. 相似文献
127.
128.
An efficient access to 1,1-diarylethylenes of biological interest by coupling functionalized aryl Grignard reagents and 1-arylvinyl halides in the presence of FeCl(3)/CuTC is described. This bimetallic system proved to be superior to the use of Fe or Cu catalyst alone. The synthetic utility of this protocol is illustrated in the field of steroid chemistry. 相似文献
129.
Aldolic condensations with 0-ethyl thioesters are performed on basic alumina to give 2,3-unsaturated thioates. The stereochemistry of the reaction is discussed and compared with Knoevenagel's, Pinner's and Wittig-Horner's reactions. 相似文献
130.