全文获取类型
收费全文 | 82篇 |
免费 | 4篇 |
专业分类
化学 | 61篇 |
晶体学 | 1篇 |
数学 | 4篇 |
物理学 | 20篇 |
出版年
2023年 | 1篇 |
2020年 | 3篇 |
2019年 | 2篇 |
2018年 | 1篇 |
2017年 | 1篇 |
2016年 | 3篇 |
2014年 | 4篇 |
2013年 | 8篇 |
2012年 | 6篇 |
2011年 | 8篇 |
2010年 | 1篇 |
2009年 | 1篇 |
2008年 | 3篇 |
2007年 | 2篇 |
2006年 | 4篇 |
2005年 | 5篇 |
2004年 | 3篇 |
2003年 | 2篇 |
2000年 | 1篇 |
1999年 | 3篇 |
1998年 | 4篇 |
1997年 | 1篇 |
1996年 | 1篇 |
1994年 | 1篇 |
1992年 | 1篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1988年 | 1篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1980年 | 1篇 |
1979年 | 1篇 |
1978年 | 2篇 |
1976年 | 1篇 |
1973年 | 1篇 |
1970年 | 1篇 |
1967年 | 2篇 |
1966年 | 1篇 |
排序方式: 共有86条查询结果,搜索用时 15 毫秒
61.
62.
63.
64.
65.
66.
67.
68.
69.
Bianca Antonioli David J. Bray Jack K. Clegg Katrina A. Jolliffe Kerstin Gloe Karsten Gloe Leonard F. Lindoy 《Polyhedron》2007
Three copper(II) complexes derived from 2-(hydroxymethyl)pyridine (LH) have been synthesised and a comparative X-ray investigation of their respective crystal structures undertaken. In the absence of added base, LH reacts with copper(II) chloride or nitrate to yield the five-coordinate [Cu(LH)2Cl]Cl and six-coordinate [Cu(LH)2(NO3)2] species. In the chloro complex the coordination geometry is distorted trigonal bipyramidal, with the pyridyl nitrogens occupying the axial position and two hydroxyl oxygens from the bidentate ligands together with a chloro group occupying the equatorial sites. The structure of the nitrate species, published previously, has been reinvestigated at low temperature in order to specify the weak interactions in the crystal; it contains two molecules of bidentate LH bound trans in the equatorial plane while monodentate nitrato ligands occupy the axial sites. In each of these complexes the hydroxyl protons act as hydrogen bond donors, interacting with the non-coordinated chloride anion in [Cu(LH)2Cl]Cl and the coordinated nitrato groups in [Cu(LH)2(NO3)2] to form bridged, hydrogen-bonded, copper(II)-organic arrays in each case; offset face-to-face π-stacking in the latter produces a two dimensional structure. Further weak CH?Cl, CH?O interactions stabilise both arrangements. The X-ray structure of the complex [Cu(L)2] · 4H2O containing the deprotonated ligand is also described. The presence of the latter results in the above hydrogen bonding arrangements being ‘switched off’ and instead a new two-dimensional network involving bridging tetrameric water clusters hydrogen bound to adjacent ligand hydroxo groups to give extended sheets is generated; offset face-to-face π-stacking occurs between sheets to yield a three dimensional array. 相似文献
70.
Clegg JK Bray DJ Gloe K Gloe K Jolliffe KA Lawrance GA Lindoy LF Meehan GV Wenzel M 《Dalton transactions (Cambridge, England : 2003)》2008,(10):1331-1340
Uncharged complexes, formulated as trimeric metallocycles of type [M3(L(1))3(Py)6] (where M = cobalt(II), nickel(II) and zinc(II) and L(1) is the doubly deprotonated form of a 1,4-phenylene linked bis-beta-diketone ligand of type 1,4-bis(RC(O)CH2C(O))C6H4 (R = t-Bu)) have been synthesised, adding to related, previously reported complexes of these metals with L(1) (R = Ph) and copper(ii) with L(1) (R = Me, Et, Pr, t-Bu, Ph). New lipophilic ligand derivatives with R = hexyl, octyl or nonyl were also prepared for use in solvent extraction experiments. The X-ray structures of H2L(1) (R = t-Bu) and of its trinuclear (triangular) nickel(II) complex [Ni3(L(1))3(Py)6].3.5Py (R = t-Bu) are also presented. Electrochemical studies of H2L(1), [Co3(L(1))3(Py)6], [Ni3(L(1))3(Py)6], [Cu3(L(1))3], [Zn3(L(1))3(Py)6] and [Fe4(L(1))6] (all with R = t-Bu) show that oxidative processes for the complexes are predominantly irreversible, but several examples of quasireversible behaviour also occur and support the assignment of an anodic process, seen between +1.0 and +1.6 V, as involving metal-centred oxidations. The reduction behaviour for the respective metal complexes is not simple, being irreversible in most cases. Solvent extraction studies (water/chloroform) involving the systematic variation of the metal, bis-beta-diketone and heterocyclic base concentrations have been performed for cobalt(II) and zinc(II) using a radiotracer technique in order to probe the stoichiometries of the respective extracted species. Significant extraction synergism was observed when 4-ethylpyridine was also present with the bis-beta-diketone ligand in the chloroform phase. Competitive extraction studies demonstrated a clear uptake preference for copper(II) over cobalt(II), nickel(II), zinc(II) and cadmium(II). 相似文献