THE ANOMERIC EFFECT IN DITHIATRIAZINES

被引:6
|
作者
JAUDASPREZEL, E
MAGGIULLI, R
MEWS, R
OBERHAMMER, H
PAUST, T
STOHRER, WD
机构
[1] UNIV BREMEN,INST ANORGAN & PHYS CHEM,LEOBENERSTR NW 2,W-2800 BREMEN 33,GERMANY
[2] UNIV BREMEN,INST ORGAN CHEM,W-2800 BREMEN 33,GERMANY
[3] UNIV TUBINGEN,INST PHYS & THEORET CHEM,W-7400 TUBINGEN 1,GERMANY
关键词
1λ[!sup]4[!/sup; 3λ[!sup]4[!/sup]‐Dithiatriazines; Anomeric effect; Calculations; MNDO; Electron diffraction;
D O I
10.1002/cber.19901231107
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Anomeric Effect in Dithiatriazines From (CF3CN3S2)n (1) and XeF2, Br2, or (CF3)2NO* the corresponding S,S‐substituted dithiatriazines CF3CN3S2F2 (2), CF3CN3S2Br2 (3), and CF3CN3S2[ON(CF3)2]2 (4) are prepared. An electron diffraction study of 2 in the gas phase results in a slightly aplanar 6‐membered ring with chair conformation and both S‐F bonds in axial position. MNDO calculations show that the position of the substituents at the sulfur atoms is strongly dependent on these substituents and on the ring geometry. The cis preference is the result of an anomeric effect. Copyright © 1990 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
引用
收藏
页码:2123 / 2127
页数:5
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