2000
DOI: 10.1016/s0022-328x(00)00327-2
|View full text |Cite
|
Sign up to set email alerts
|

Electroreductive synthesis of oligosilanes and polysilanes with ordered sequences

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
26
0

Year Published

2005
2005
2023
2023

Publication Types

Select...
5
2
2

Relationship

1
8

Authors

Journals

citations
Cited by 37 publications
(26 citation statements)
references
References 24 publications
0
26
0
Order By: Relevance
“…Although there exist several papers in the literature dealing with the electrochemical formation of methylated or phenylated disilanes [18][19][20][21], much less attempts have been made to reduce chlorosilanes bearing one or more functional groups on the silicon atom. Besides a patent claiming the formation of 1,2-difunctional disilanes by the electrolysis of chlorosilanes R 0 R 2 SiCl (R 0 = Me, Ph, MeO, allyl, octyl) in THF with various supporting electrolytes and two metal electrodes [17], to the best of our knowledge only one publication exists dealing with the electrohemical Si-Si bond formation starting from a functional chlorosilane: the formation of 1,3-dihydrotrisilanes by co-electrolysis of HMe 2 SiCl and Ph 2 SiCl 2 with Mg electrodes in THF/LiClO 4 [19].…”
Section: Electrochemical Synthesis Of 12-difunctional Disilanesmentioning
confidence: 99%
See 1 more Smart Citation
“…Although there exist several papers in the literature dealing with the electrochemical formation of methylated or phenylated disilanes [18][19][20][21], much less attempts have been made to reduce chlorosilanes bearing one or more functional groups on the silicon atom. Besides a patent claiming the formation of 1,2-difunctional disilanes by the electrolysis of chlorosilanes R 0 R 2 SiCl (R 0 = Me, Ph, MeO, allyl, octyl) in THF with various supporting electrolytes and two metal electrodes [17], to the best of our knowledge only one publication exists dealing with the electrohemical Si-Si bond formation starting from a functional chlorosilane: the formation of 1,3-dihydrotrisilanes by co-electrolysis of HMe 2 SiCl and Ph 2 SiCl 2 with Mg electrodes in THF/LiClO 4 [19].…”
Section: Electrochemical Synthesis Of 12-difunctional Disilanesmentioning
confidence: 99%
“…Besides a patent claiming the formation of 1,2-difunctional disilanes by the electrolysis of chlorosilanes R 0 R 2 SiCl (R 0 = Me, Ph, MeO, allyl, octyl) in THF with various supporting electrolytes and two metal electrodes [17], to the best of our knowledge only one publication exists dealing with the electrohemical Si-Si bond formation starting from a functional chlorosilane: the formation of 1,3-dihydrotrisilanes by co-electrolysis of HMe 2 SiCl and Ph 2 SiCl 2 with Mg electrodes in THF/LiClO 4 [19].…”
Section: Electrochemical Synthesis Of 12-difunctional Disilanesmentioning
confidence: 99%
“…These studies, however, have been rather limited to the reduction of alkyl-or aryl-substituted chlorosilanes, and much less is known for those bearing functional groups. A few years ago, Kashimura et al showed that hydrochlorosilanes can be cross-coupled electrochemically with dichloromono-, di-and trisilanes to afford a,xdihydrooligosilanes, respectively [6]. More recently, Grogger et al reported similar synthesis of 1,2-dihydrodisilanes by anodic homo-coupling reactions of chlorohydrosilanes [7].…”
Section: Introductionmentioning
confidence: 99%
“…Stepwise synthesis of oligosilanes [22,23] This method is also applicable to the synthesis of trisilanes and tetrasilanes. For example, the electroreductive cross coupling of organodichlorosilanes (3) with chlorotrimethylsilane (1b) (5 equivalent to 3) gave the corresponding trisilanes 4 in moderate to good material yields (Scheme 5) and that of 1,2-dichloro-1,1,2-trimethyl-2-phenyldisilane (5) and 1b (5 equivalent to 5) gave tetrasilane 6 in 55% yield (Scheme 6).…”
mentioning
confidence: 99%