全文获取类型
收费全文 | 134篇 |
免费 | 22篇 |
国内免费 | 10篇 |
专业分类
化学 | 119篇 |
晶体学 | 2篇 |
力学 | 3篇 |
综合类 | 2篇 |
物理学 | 40篇 |
出版年
2023年 | 6篇 |
2022年 | 3篇 |
2021年 | 2篇 |
2020年 | 11篇 |
2019年 | 7篇 |
2018年 | 5篇 |
2017年 | 5篇 |
2016年 | 10篇 |
2015年 | 7篇 |
2014年 | 8篇 |
2013年 | 21篇 |
2012年 | 14篇 |
2011年 | 1篇 |
2010年 | 3篇 |
2009年 | 3篇 |
2008年 | 7篇 |
2007年 | 5篇 |
2006年 | 3篇 |
2005年 | 5篇 |
2004年 | 5篇 |
2003年 | 6篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1999年 | 3篇 |
1998年 | 1篇 |
1997年 | 2篇 |
1996年 | 1篇 |
1995年 | 2篇 |
1994年 | 3篇 |
1993年 | 1篇 |
1992年 | 2篇 |
1990年 | 1篇 |
1988年 | 1篇 |
1984年 | 2篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1978年 | 1篇 |
1976年 | 1篇 |
1974年 | 1篇 |
排序方式: 共有166条查询结果,搜索用时 234 毫秒
21.
A new set of trial functions for 1s^22sns configurations in a beryllium atom is suggested. A Mathematica program based on the variational method is developed to calculate the wavefunctions and energies of 1s^22sns (n = 3 - 6) configurations in a beryllium atom. Non-relativistic energy, polarization correction and relativistic correction which include mass correction, one- and two-body Darwin corrections, spin-spin contact interaction and orbit-orbit interaction, are calculated respectively. The results are in good agreement with experimental data. 相似文献
22.
23.
Masataka Hiraide Kennich Ishikawa Zuo Sheng Chen Hiroshi Kawaguchi 《Mikrochimica acta》1994,117(1-2):7-13
Coprecipitation first with magnesium hydroxide, next with tin(IV) hydroxide is developed for the determination of traces of beryllium in sea-water. To a 200-ml sample is added a sodium hydroxide solution to form magnesium hydroxide at pH 11.5, on which beryllium is quantitatively coprecipitated. The precipitate is separated by centrifugation and dissolved in 2 ml of 12 mol/l hydrochloric acid. The resulting solution (ca. 10 ml) is mixed with 2 mg of tin (IV) carrier and the pH is adjusted to 5.0 to collect the beryllium on tin (IV) hydroxide, leaving magnesium ions in the solution. The tin (IV) hydroxide is centrifuged, dissolved in 0.1 ml of 5 mol/l hydrobromic acid, and then diluted to 1 ml with water. Magnesium is so added as to be 500 g/ml for increasing the sensitivity about four times, and the beryllium in the solution is determined by graphite furnace atomic absorption spectrometry. The experiments with synthetic seawater samples showed that pg — g amounts of beryllium can be coprecipitated on the metal hydroxides and beryllium at the low ng/1 level can be determined with reasonable precision (RSD < 10%). The detection limit of the proposed method is 0.5 ng/l of beryllium in seawater. 相似文献
24.
对300余个样品进行监测,选择灵敏度高的石墨管和最佳基体,提高灰化、原子化的温度,确立了石墨炉原子吸收法测定空气中铍含量的实验条件。样品采用干灰化消解法,最佳溶剂为质量分数l%的硝酸溶液,利用仪器内置的样品浓度计算程序,绘制工作曲线直接获得样品中铍的含量。方法检出限为0.021μg/L,测定结果的相对标准偏差小于2%(n=6),线性范围为0~6.5μg/L,加标回收率为91.6%~107%。 相似文献
25.
26.
27.
Dr. Florian Kraus Dipl.‐Chem. Sebastian A. Baer Dr. Magnus R. Buchner Dr. Antti J. Karttunen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(7):2131-2142
The first structural characterization of the text‐book tetraammineberyllium(II) cation [Be(NH3)4]2+, obtained in the compounds [Be(NH3)4]2Cl4 ? 17NH3 and [Be(NH3)4]Cl2, is reported. Through NMR spectroscopic and quantum chemical studies, its hydrolysis products in liquid ammonia were identified. These are the dinuclear [Be2(μ‐OH)(NH3)6]3+ and the cyclic [Be2(μ‐OH)2(NH3)4]2+ and [Be3(μ‐OH)3(NH3)6]3+ cations. The latter species was isolated as the compound [Be3(μ‐OH)3(NH3)6]Cl3 ? 7NH3. NMR analysis of solutions of BeF2 in liquid ammonia showed that the [BeF2(NH3)2] molecule was the only dissolved species. It acts as a strong fluoride‐ion acceptor and forms the [BeF3(NH3)]? anion in the compound [N2H7][BeF3(NH3)]. The compounds presented herein were characterized by single‐crystal X‐ray structure analysis, 9Be, 17O, and 19F NMR, IR, and Raman spectroscopy, deuteration studies, and quantum chemical calculations. The extension of beryllium chemistry to the ammine system shows similarities but also decisive differences to the aquo system. 相似文献
28.
29.
Previous studies describe derivatization of metal ions followed by analysis using gas chromatography, usually on packed columns. In many of these studies, stable and volatile derivatives were formed using fluorinated β‐diketonate reagents. This paper extends previous work by investigating separations of the derivatives on small‐diameter capillary gas chromatography columns and exploring on‐fiber, solid‐phase microextraction derivatization techniques for beryllium. The β‐diketonate used for these studies was 1,1,1,2,2,6,6,7,7,7‐decafluoro‐3,5‐heptanedione. Derivatization of lanthanides also required addition of a neutral donor, dibutyl sulfoxide, in addition to 1,1,1,2,2,6,6,7,7,7‐decafluoro‐3,5‐heptanedione. Unoptimized separations on a 100‐μm i.d. capillary column proved capable of rapid separations (within 15 min) of lanthanide derivatives that are adjacent to one another in the periodic table. Full‐scan mass spectra were obtained from derivatives containing 5 ng of each lanthanide. Studies also developed a simple on‐fiber solid‐phase microextraction derivatization of beryllium. Beryllium could be analyzed in the presence of other alkali earth elements (Ba(II) and Sr(II)) without interference. Extension of the general approach was demonstrated for several additional elements (i.e. Cu(II), Cr(III), and Ga(III)). 相似文献
30.
Theoretical Study on Dissociation Mechanisms of Di-ethyl Berylliums and Di-t-butyl Berylliums 下载免费PDF全文
Ling-biao Meng Yan Zhao Ji-qiang Zhang Ji-cheng Zhang Wei-dong Wu Zhuo Wang 《化学物理学报(中文版)》2014,27(2):168-174
The potential energy surfaces (PES) of unimolecular dissociation reactions for di-ethyl beryl-lium and di-t-butyl beryllium are investigated by B3LYP, CCSD(T), and G3B3 approaches. Possible reaction pathways through either the radical or transition state (TS) of the molecules are considered. The geometries, vibrational frequencies and relative energies for various sta-tionary points are determined. From the study of energetics, the TS pathways arising from concerted molecular eliminations are indicated to be the main dissociation pathways for both molecules. The PES differences of the dissociation reactions are investigated. The activa-tion energies and rate constants will be helpful for investigating the predictive ability of the reaction in further theoretical and experimental research. 相似文献