## Dedicated to Professor Herbert W. Roesky on the occasion of his 65th birthday By attempting to generate a cationic, possibly solvated, vinylideneruthenium(ii) complex with a 14-electron configuration at the metal center, we recently found that the reaction of the starting material 1 with HBF 4
Regiospecific Hydroxylation of Metallodisilanes of the Iron Group – An Impressive Example of the Transition Metal Effect
✍ Scribed by Wolfgang Malisch; Heinrich Jehle; Stephan Möller; Chantu Saha-Möller; Waldemar Adam
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 133 KB
- Volume
- 1998
- Category
- Article
- ISSN
- 1434-1948
No coin nor oath required. For personal study only.
✦ Synopsis
Reaction of the ferriodisilanes C 5 R 5 (OC) 2 Fe-Si 2 H 5 [R = H C 5 H 5 (OC) 2 Fe-Si 2 Cl 5 (4a) and C 5 Me 5 (OC) 2 Ru-Si 2 Cl 5 (4b) with water results in regiospecific hydroxylation of the β-(1a), Me (1b)] with dimethyldioxirane leads to selective insertion of oxygen into the α-Si-H bonds to yield the silicon atom to generate metallodisilanetriols C 5 R 5 (OC) 2 M-SiCl 2 -Si(OH) 3 [M = Fe, R = H (5a); M = Ru, R = Me (5b)]. ferriodihydroxydisilanes C 5 R 5 (OC) 2 Fe-Si(OH) 2 -SiH 3 [R = H (2a), Me (2b)]. Another access to yield 2a is opened by Controlled condensation of 5b with Me 2 Si(H)Cl leads to the novel rutheniosiloxane C 5 Me 5 (OC) 2 Ru-SiCl 2 -Si(OSiMe 2 H) 3 hydrolysis of the dichloro(ferrio)disilane Cp(OC) 2 Fe-SiCl 2 -SiH 3 (3a). Treatment of the pentachloro(metallo)disilanes (6).
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