Diselenadiphosphetane diselenides and triselenadiphospholane diselenides -: Synthesis and characterization by 31P and 77Se solid-state MNR spectroscopy

被引:0
|
作者
Grossmann, G [1 ]
Ohms, G
Krüger, K
Karaghiosoff, K
Eckstein, K
Hahn, J
Hopp, A
Malkina, OL
Hrobarik, P
机构
[1] Tech Univ Dresden, Inst Analyt Chem, D-01062 Dresden, Germany
[2] Univ Munich, Inst Anorgan Chem, D-8000 Munich, Germany
[3] Univ Cologne, Inst Anorgan Chem, D-5000 Cologne, Germany
来源
关键词
1,3-diselena-2,4-diphosphetane-2,4-diselenides; 1,2,4-triselena-3,5-diphospholane-3,5-diselenides; small ring systems; NMR spectroscopy; phosphorus; selenium;
D O I
10.1002/1521-3749(200106)627:6<1269::AID-ZAAC1269>3.0.CO;2-Q
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
1,3-Diselena-2,4-diphosphetane-2,4-diselenides (RPSe(2))(2) with R = Me, Et, t-Bu, Ph, 4-Me(2)NC(6)H(4), 4-MeOC(6)H(4) have been synthesized by different methods. The insoluble compounds were investigated by (31)P and (77)Se solid-state NMR and the purity of the compounds has been checked by their CP MAS sideband NMR spectra. The structure of the investigated compounds has been confirmed by the isotropic and anisotropic values of the chemical shifts and the (1)J(P-Se) coupling constants. In addition, two new 1,2,4-triselena-3,5-diphospholane-3,5-diselenides, (RPSe(2))(2)Se (R = Me, Et), formed under similar synthesis conditions, were investigated. Their structure was derived from the (77)Se satellites (31)P solution spectra and from solid-state spectra. For (t-BuPSe(2))(2) the experimentally obtained principal values of phosphorus and selenium shielding tensors are compared with values from IGLO calculations (HF und SOS DFPT). The calculated orientations of the principal axes are discussed.
引用
收藏
页码:1269 / 1278
页数:10
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