Treatment of hexakis(2, 4, tetrasilabuta-1,3-diene (1), R 2 Si=SiR±SiR=SiR 2 , with ammonia and chlorine furnishes the correspondingly substituted 1,4diaminotetrasilane (3) and 1,2,3,4-tetrachlorotetrasilane (6). While product 6 crystallizes as a racemate, 3 forms a con-glomerate of enantiomerical
Oxygen and Water Additions to a Tetrasilabuta-1,3-diene
✍ Scribed by Stefan Willms; Andreas Grybat; Wolfgang Saak; Manfred Weidenbruch; Heinrich Marsmann
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- German
- Weight
- 137 KB
- Volume
- 626
- Category
- Article
- ISSN
- 0372-7874
No coin nor oath required. For personal study only.
✦ Synopsis
The reaction of hexakis(2,4,6-triisopropylphenyl)tetrasilabuta-1,3-diene R 2 Si=SiR±SiR=SiR 2 (1) with atmospheric oxygen furnishes the oxidation product R 2 Si(O) 2 SiROSiR(O) 2 SiR 2 (5) by oxygen insertion into all Si±Si bonds. However, treatment of 1 with meta-chloroperoxobenzoic acid provides R 2 Si(O) 2 SiR±SiR(O) 2 SiR 2 (7) with retention of the Si±Si single bond. Reaction of 1 with traces of water gives the oxatetrasilacyclopentane derivative 10 analogous to THF. With excess water a tetrasilane-1,4-diol is formed. The structures of 5, 7, and 10 were determined by X-ray crystallography.
📜 SIMILAR VOLUMES
ses. Their relative total energies are 0, 0.4, 4.4 and -3.6 kcalmol-I , respectively.1111 Although the difference in energy between the (q2-0,C-HNCO)(q2-C,N-HNCO) and (q2-C,N-HNCO), isomers is small, the calculations are inconsistent with the observed structure. Next, we used molecular mechanics ca