排序方式: 共有65条查询结果,搜索用时 15 毫秒
1.
2.
Gerard A. van Albada Ilpo Mutikainen Urho Turpeinen Jan Reedijk 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(3):m179-m181
The title mononuclear complex, [Cu(CO3)(C8H7N5)(H2O)]·2H2O, was obtained by fixation of CO2 by a mixture of copper(II) tetrafluoroborate and the ligand bis(pyrimidin‐2‐yl)amine in ethanol/water. The CuII ion of the complex has a distorted square‐pyramidal environment, with a basal plane formed by two N atoms of the ligand and two chelating O atoms of the carbonate group, while the apical position is occupied by the O atom of the coordinating water molecule. In the solid state, hydrogen‐bonding interactions are dominant, the most unusual being the Watson–Crick‐type coplanar ligand pairing through two N—H?N bonds. Lattice water molecules also participate in hydrogen bonding. 相似文献
3.
Tandem mass spectrometric analysis of S‐ and N‐linked glutathione conjugates of pulegone and menthofuran and identification of P450 enzymes mediating their formation
下载免费PDF全文
![点击此处可从《Rapid communications in mass spectrometry : RCM》网站下载免费的PDF全文](/ch/ext_images/free.gif)
4.
Gerard A. van Albada Maarten G. van der Horst Simon J. Teat Patrick Gamez Olivier Roubeau Ilpo Mutikainen Urho Turpeinen Jan Reedijk 《Polyhedron》2009
In this study the synthesis, crystal structure and characterization of three new transition metal polynuclear compounds with formula [Cu(dipm)(μ-dca)2]n(H2O) (1), [Ni(dipm)(μ-dca)2]n(C2H6O)1/2 (2) and [Cd(dipm)(μ-dca)2]n (3) (in which dipm = bis(pyrimidin-2-yl)amine and dca = dicyanamide) are reported. The isostructural compounds 1 and 2 contain a double-bridging end-to-end dca unit connecting two metal ions and a single bridging end-to-end dca unit between subsequent metals. Compound 3 exhibits only single bridging end-to-end dca units, oriented in three directions, giving rise to a 3D framework. 相似文献
5.
6.
7.
Gerard A. van Albada Ilpo Mutikainen Urho Turpeinen Jan Reedijk 《Journal of chemical crystallography》2001,31(2):75-79
The first high-spin iron(III) compound with the ligand 2,2-bipyridine-1,1-dioxide (abbreviated as bpdo) is reported. The compound [Fe(bpdo)3](ClO4)3(CH3CN)2 crystallizes in the space group P
, with a = 11.767(3), b = 13.166(4), c = 15.951(4) Å, = 104.62(3), = 101.66(3), = 112.14(3)°, and Z = 2. The Fe(III) atom is octahedrally surrounded by six oxygen atoms of three bpdo ligands. In the far-infrared region the Fe—O vibration is observed at 411 cm–1. The magnetic susceptibility reveals a of 6.04 ± 0.04 BM in the 10–280 K region, typical of high-spin Fe(III). 相似文献
8.
Lu Z Costa JS Roubeau O Mutikainen I Turpeinen U Teat SJ Gamez P Reedijk J 《Dalton transactions (Cambridge, England : 2003)》2008,(27):3567-3573
A new bifunctional, triazine-based ligand has been designed with the aim to generate a copper(II) complex holding a TEMPO (2,2,6,6-tetramethylpiperidinyloxy) moiety. The coordination compound obtained from the ligand 4-(2-(3-(pyridin-2-yl)-1H-pyrazol-1-yl)ethoxy)-6-(4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl)-N,N-diphenyl-1,3,5-triazin-2-amine (pypzt-1) and copper(II) bromide (i.e. complex 8) is capable of catalysing the selective, aerobic oxidation of benzyl alcohol to 84% of benzaldehyde in 24 h. This "galactose oxidase activity" of the copper/TEMPO complex is observed as well for the conversion of the non-activated alkyl alcohol octan-1-ol to octanal with a yield of 29% after the same reaction time. The single-crystal X-ray structure of 8 shows that its crystal lattice contains [Cu(I)Br(2)](-) anions which appear to be stabilised by means of both anion-pi and hydrogen bonding interactions. In addition, the solid state structure of 8 exhibits (lone-pair)-pi interactions between the nitrogen atom of an acetonitrile molecule and a triazine ring. The magnetic properties of 8 have been investigated by EPR and magnetic susceptibility measurements. 相似文献
9.
Adriana González Castro José Sánchez Costa Roberta Pievo Chiara Massera Ilpo Mutikainen Urho Turpeinen Patrick Gamez Jan Reedijk Prof. Dr. 《无机化学与普通化学杂志》2008,634(14):2477-2482
A new Schiff‐base ligand having a potentially coordinating thioether group (2‐quinoline‐N‐(2′‐methylthiophenyl)methyleneimine, qmtpm ) has been prepared. The synthesis, structure, UV‐Vis and EPR studies of one copper(II) and two cobalt(II) complexes from this ligand is reported. The X‐ray structures of the CuII and CoII chlorido complexes 1 and 2 reveal the metal atoms in highly distorted square‐pyramidal environments constituted of one tridentate ligand and two anions. On the other hand, the thiocyanato CoII compound 3 exhibits a distorted trigonal‐bipyramidal structure. These structural variations are apparently due to the different counter‐ions which leads to distinct lattice interactions. The spectroscopic data obtained by EPR and UV‐Vis investigations are in agreement with the solid‐state structures of the coordination compounds. 相似文献
10.