Synthesis and NMR investigation of selenobutyl substituted silanes and oligosilanes

Authors
Citation
U. Herzog, Synthesis and NMR investigation of selenobutyl substituted silanes and oligosilanes, J PRAK CH C, 342(4), 2000, pp. 379-388
Citations number
17
Categorie Soggetti
Chemistry
Journal title
JOURNAL FUR PRAKTISCHE CHEMIE-CHEMIKER-ZEITUNG
ISSN journal
09411216 → ACNP
Volume
342
Issue
4
Year of publication
2000
Pages
379 - 388
Database
ISI
SICI code
0941-1216(2000)342:4<379:SANIOS>2.0.ZU;2-C
Abstract
The reaction of BuSeLi, made from BuLi and elemental selenium, with chloros ilanes MexPhySiCl4-x-y led to selenobutyl substituted derivatives. In the c ases of polychlorosilanes formation of the completely substituted products MexPhySi(SeBu)(4-x-y) are favoured. Higher yields of partially substituted products could be obtained by reaction of chlorosilanes with BuSeH/NEt3. Be sides monosilanes the reactions of several methylchlorodi-, tri- and isotet rasilanes with BuSeLi and BuSeH/NEt3 were also investigated. In SiClMe(SiCl Me2)(2) the chlorine substituent at the middle silicon atom is substituted by BuSeH/NEt3 at first selectively. All products were characterized by H-1, C-13, Si-29 and Se-77 NMR and trends of chemical shifts and coupling const ants ((1)J(SiSi), (1)J(SiSe), (2)J(SiSe)) with the substitution pattern wer e investigated.