全文获取类型
收费全文 | 76篇 |
免费 | 9篇 |
专业分类
化学 | 46篇 |
力学 | 6篇 |
数学 | 4篇 |
物理学 | 29篇 |
出版年
2016年 | 1篇 |
2015年 | 5篇 |
2014年 | 3篇 |
2013年 | 2篇 |
2012年 | 6篇 |
2011年 | 15篇 |
2010年 | 2篇 |
2008年 | 7篇 |
2007年 | 2篇 |
2006年 | 1篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1999年 | 2篇 |
1998年 | 1篇 |
1996年 | 2篇 |
1995年 | 2篇 |
1994年 | 7篇 |
1993年 | 1篇 |
1992年 | 5篇 |
1991年 | 2篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1980年 | 1篇 |
1979年 | 1篇 |
1977年 | 1篇 |
1976年 | 3篇 |
1973年 | 2篇 |
排序方式: 共有85条查询结果,搜索用时 15 毫秒
31.
Dr. J. Alberto Rodríguez‐Velamazán Dr. Oscar Fabelo Dr. Christine M. Beavers Dr. Eva Natividad Dr. Marco Evangelisti Dr. Olivier Roubeau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(26):7956-7961
FeII(Metz)6](FeIIIBr4)2 (Metz=1‐methyltetrazole) is one of the rare systems combining spin‐crossover and long‐range magnetic ordering. A joint neutron and X‐ray diffraction and magnetometry study allows determining its collinear antiferromagnetic structure, and shows an increase of the Néel temperature from 2.4 K at ambient pressure, to 3.9 K at 0.95 GPa. Applied pressure also enables a full high‐spin to low‐spin switch at ambient temperature. 相似文献
32.
Zuo T Walker K Olmstead MM Melin F Holloway BC Echegoyen L Dorn HC Chaur MN Chancellor CJ Beavers CM Balch AL Athans AJ 《Chemical communications (Cambridge, England)》2008,(9):1067-1069
Although there are 51 568 non-IPR and 24 IPR structures for C84, the egg-shaped endohedral fullerenes Tm3N@C(s)(51 365)-C84 and Gd3N@C(s)(51 365)-C84 utilize the same non-IPR cage structure as found initially for Tb3N@C(s)(51 365)-C84. 相似文献
33.
Glutarimidedioxime: A Complexing and Reducing Reagent for Plutonium Recovery from Spent Nuclear Fuel Reprocessing
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Dr. Liang Xian Dr. Guoxin Tian Dr. Christine M. Beavers Dr. Simon J. Teat Dr. David K. Shuh 《Angewandte Chemie (International ed. in English)》2016,55(15):4671-4673
Efficient separation processes for recovering uranium and plutonium from spent nuclear fuel are essential to the development of advanced nuclear fuel cycles. The performance characteristics of a new salt‐free complexing and reducing reagent, glutarimidedioxime (H2A), are reported for recovering plutonium in a PUREX process. With a phase ratio of organic to aqueous of up to 10:1, plutonium can be effectively stripped from 30 % tributyl phosphate (TBP) in kerosene into 1 m HNO3 with H2A. The complexation‐reduction mechanism is illustrated with the combination of UV/Vis absorption spectra and the crystal structure of a PuIV complex with the reagent. The fast stripping rate and the high efficiency for stripping PuIV, through the complexation‐reduction mechanism, is suitable for use in centrifugal contactors with very short contact/resident times, thereby offering significant advantages over conventional processes. 相似文献
34.
Zuo T Beavers CM Duchamp JC Campbell A Dorn HC Olmstead MM Balch AL 《Journal of the American Chemical Society》2007,129(7):2035-2043
The recent finding that isomer 2 of Tb(3)N@C(84) uses one of the 51,568 possible nonisolated pentagon rule (non-IPR) structures for the C(84) cage rather than one of the 24 cage isomers that do obey the IPR suggests that further experimental work on the structure of larger endohedrals is needed to observe the utility of the IPR rule in this uncharted territory. The structures of the newly synthesized endohedral fullerenes--Tb(3)N@C(88), Tb(3)N@C(86), and the Ih and D(5)(h) isomers of Tb(3)N@C(80)--have been determined by single-crystal X-ray diffraction on samples cocrystallized with NiII(octaethylporphyrin). In contrast to the situation for isomer 2 of Tb(3)N@C(84), the structures of Tb(3)N@C(88) and Tb(3)N@C(86) do conform to the IPR. Both Tb(3)N@C(88) and Tb(3)N@C(86) have chiral structures with D(2) symmetry for Tb(3)N@C(880 and D(3) symmetry for Tb(3)N@C(86). Within this group of endohedrals, the size of the carbon cage affects the Tb-N and Tb-C distances, the orientations of the carbon cage with respect to the porphyrin plane, the locations of the metal ions and their orientations relative to the porphyrin plane, and the degree of pyramidalization of the Tb(3)N unit. 相似文献
35.
36.
Taylor SM Karotsis G McIntosh RD Kennedy S Teat SJ Beavers CM Wernsdorfer W Piligkos S Dalgarno SJ Brechin EK 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(27):7521-7530
In the cone conformation calix[4]arenes possess lower-rim polyphenolic pockets that are ideal for the complexation of various transition-metal centres. Reaction of these molecules with manganese salts in the presence of an appropriate base (and in some cases co-ligand) results in the formation of a family of calixarene-supported [Mn(III)(2)Mn(II)(2)] clusters that behave as single-molecule magnets (SMMs). Variation in the alkyl groups present at the upper-rim of the cone allows for the expression of a degree of control over the self-assembly of these SMM building blocks, whilst retaining the general magnetic properties. The presence of various different ligands around the periphery of the magnetic core has some effect over the extended self-assembly of these SMMs. 相似文献
37.
Stephanie M. Taylor Dr. Sergio Sanz Dr. Ruaraidh D. McIntosh Dr. Christine M. Beavers Dr. Simon J. Teat Prof. Euan K. Brechin Dr. Scott J. Dalgarno 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(50):16014-16022
p‐tert‐Butylcalix[4]arene is a bowl‐shaped molecule capable of forming a range of polynuclear metal clusters under different experimental conditions. p‐tert‐Butylcalix[8]arene (TBC[8]) is a significantly more flexible analogue that has previously been shown to form mono‐ and binuclear lanthanide (Ln) metal complexes. The latter (cluster) motif is commonly observed and involves the calixarene adopting a near double‐cone conformation, features of which suggested that it may be exploited as a type of assembly node in the formation of larger polynuclear lanthanide clusters. Variation in the experimental conditions employed for this system provides access to Ln1, Ln2, Ln4, Ln5, Ln6, Ln7 and Ln8 complexes, with all polymetallic clusters containing the common binuclear lanthanide fragment. Closer inspection of the structures of the polymetallic clusters reveals that all but one (Ln8) are in fact based on metal octahedra or the building blocks of octahedra, with the identity and size of the final product dependent upon the basicity of the solution and the deprotonation level of the TBC[8] ligand. This demonstrates both the versatility of the ligand towards incorporation of additional metal centres, and the associated implications for tailoring the magnetic properties of the resulting assemblies in which lanthanide centres may be interchanged. 相似文献
38.
39.
40.