SOLID-STATE AND SOLUTION STRUCTURES OF 3 LITHIUMSULFINIMIDAMIDES - IDENTIFICATION OF 2 DISTINCT STRUCTURAL TYPES

被引:49
作者
EDELMANN, FT
KNOSEL, F
PAUER, F
STALKE, D
BAUER, W
机构
[1] UNIV GOTTINGEN,INST ANORGAN CHEM,TAMMANNSTR 4,W-3400 GOTTINGEN,GERMANY
[2] UNIV ERLANGEN NURNBERG,INST ORGAN CHEM,W-8520 ERLANGEN,GERMANY
关键词
D O I
10.1016/0022-328X(92)88001-Y
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The bidentate sulfinimidamide ligand has almost the same bulk as the cyclopentadienyl ligand. Two distinct structural types of highly reactive lithium sulfinimidamides, commonly used reagents, have been identified by X-ray diffraction and solution NMR studies. In the crystalline state the diethyl ether adducts [(Me3SiN)2S(C6H5)Li]2.Et2O and [(Me3SiN)(tBuN)S(C6H5)Li]2.Et2O adopt a twisted tricyclic structure with both a four coordinate and a three coordinate lithium atom in the same aggregate. The H-1 NMR spectra at various temperatures and the low temperature phase-sensitive Li-6, H-1 HOESY NMR experiment show that this structure is essentially retained in solution. The smaller bulk and higher polarity of tetrahydrofuran compared with diethyl ether results in the coordination of two solvent molecules to give [(Me3SiN)2S(C6H5)Li.THF]2, which has a centrosymmetric stair-shaped tricyclic structure consisting of three fused four-membered rings.
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页码:1 / 10
页数:10
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