全文获取类型
收费全文 | 182篇 |
免费 | 3篇 |
专业分类
化学 | 164篇 |
晶体学 | 4篇 |
物理学 | 17篇 |
出版年
2022年 | 3篇 |
2021年 | 1篇 |
2019年 | 2篇 |
2016年 | 2篇 |
2014年 | 1篇 |
2013年 | 4篇 |
2012年 | 11篇 |
2011年 | 4篇 |
2010年 | 6篇 |
2009年 | 7篇 |
2008年 | 7篇 |
2007年 | 13篇 |
2006年 | 11篇 |
2005年 | 6篇 |
2004年 | 15篇 |
2003年 | 6篇 |
2002年 | 4篇 |
2001年 | 8篇 |
2000年 | 4篇 |
1999年 | 5篇 |
1998年 | 4篇 |
1996年 | 1篇 |
1994年 | 3篇 |
1993年 | 2篇 |
1991年 | 4篇 |
1990年 | 1篇 |
1989年 | 3篇 |
1987年 | 2篇 |
1986年 | 1篇 |
1985年 | 5篇 |
1984年 | 5篇 |
1983年 | 4篇 |
1982年 | 4篇 |
1981年 | 3篇 |
1980年 | 6篇 |
1979年 | 4篇 |
1978年 | 2篇 |
1977年 | 1篇 |
1976年 | 2篇 |
1975年 | 3篇 |
1974年 | 2篇 |
1973年 | 2篇 |
1972年 | 1篇 |
排序方式: 共有185条查询结果,搜索用时 15 毫秒
121.
Hamidi S Deacon GB Junk PC Neumann P 《Dalton transactions (Cambridge, England : 2003)》2012,41(12):3541-3552
Rare earth metals activated with ca. 2% iodine react directly with 2,6-diisopropylphenol (HOdip) in tetrahydrofuran (thf), 1,2-dimethoxyethane (dme), and dig-dme (dig = di(2-methoxyethyl) ether) to give solvated phenolate complexes [Ln(Odip)(3)(thf)(n)] (Ln = La, Nd, n = 3; Ln = Sm, Dy, Y, Yb, n = 2), [Eu(Odip)(μ-Odip)(thf)(2)](2), [Ln(Odip)(3)(dme)(2)] (Ln = La, Yb) and [La(Odip)(3)(dig)] in good yield for Ln = La, Nd, Eu but modest yield for smaller Ln metals under comparable conditions. However, increasing the excess of metal greatly increased the yield for Ln = Y. The synthetic method has general potential, at least for lanthanoid phenolates. Comparison redox transmetallation/protolysis (RTP) reactions between Ln metals, Hg(C(6)F(5))(2) and the phenol gave higher yields in shorter time and, for Eu, gave [Eu(Odip)(3)(thf)(3)] in contrast to an Eu(II) complex from Eu(I(2)). New [Ln(Odip)(3)(thf)(3)] complexes have fac-octahedral structures and [Ln(Odip)(3)(thf)(2)] monomeric five coordinate distorted trigonal bipyramidal structures with apical thf ligands. [Eu(Odip)(μ-Odip)(thf)(2)](2) is an unsymmetrical dimer with two bridging Odip ligands. One five coordinate Eu atom has distorted trigonal bipyramidal stereochemistry and the other is distorted square pyramidal. Whilst [La(Odip)(3)(dme)(2)] has irregular seven coordination with mer-Odip and chelating dme ligands, [Ln(Odip)(3)(dme)(2)] (Ln = Dy, Y (prepared by ligand exchange), Yb) are monomeric six coordinate with one chelating and one unidentate dme. A six coordinate fac-octahedral arrangement is observed in [La(Odip)(3)(dig)]. 相似文献
122.
Reaction of sodium cyclopentadienide with dipyridinium hexachlorocerate(IV) in tetrahydrofuran yields tris(cyclopentadienyl)cerium(III) and not tetrakis(cyclopentadienyl)cerium(IV). 相似文献
123.
124.
125.
126.
Zelakiewicz BS Lica GC Deacon ML Tong Y 《Journal of the American Chemical Society》2004,126(32):10053-10058
On 13C1-labeled octanethiol-protected 2.7 nm Pd nanoparticle surfaces, it has been observed that the 13C1 NMR of the alpha-carbon shows a peak centered around 38 ppm (with respect to tetramethylsilane (TMS)), which virtually coincides with that of the alpha-carbons in a dioctyl-disulfide molecule (39.3 ppm), and the corresponding 13C1 spin-spin relaxation becomes nonexponential. In addition, the infrared spectrum of the same sample shows that the ligands have a 100% gauche conformation, which is also consistent with a dioctyl-disulfide arrangement. By comparing with data obtained on 13C1-labeled octanethiol-protected 2.8 nm Au nanoparticles, we propose that a dioctyl-disulfide structure of the ligands is formed on the octanethiol-protected Pd nanoparticle surface, in contrast to the thiolate structure proposed on the Au nanoparticles. In addition, CO adsorption experiments show no sign of a PdS layer formed on the Pd nanoparticle surface. Furthermore, data taken over a period of more than 1 year show that the Pd nanoparticles are rather stable in organic solvents (for instance benzene), although slow degradation does happen and oxygen seems to play an important role in accelerating the degradation. 相似文献
127.
128.
129.
D. A. G. Deacon 《Applied Physics A: Materials Science & Processing》1979,19(1):97-104
A one-dimensional linearized analysis of a storage-ring laser is developed. The dynamic and equilibrium behavior of the energy
spread, bunch length, and correlation are derived analytically through a formalism generally applicable to linear difference
equations. The limits on the applicability of the linear approximation are discussed. 相似文献
130.