2000
DOI: 10.1002/(sici)1099-0690(200002)2000:3<479::aid-ejoc479>3.0.co;2-#
|View full text |Cite
|
Sign up to set email alerts
|

Conformation and Stereodynamics of Aliphatic Triisopropylsilanes in Solution and in the Solid State

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

2002
2002
2007
2007

Publication Types

Select...
4
1

Relationship

2
3

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 24 publications
0
4
0
Order By: Relevance
“…There has already been some exploration,7−11 of the conformational possibilities for three isopropyl or similar groups attached to a tetrahedral atom, including triisopropylsilyl groups 10,11. The most recent report11 includes results both in solution and the solid state for compound 13 with a TIPS group attached to the 1‐position in naphthalene.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…There has already been some exploration,7−11 of the conformational possibilities for three isopropyl or similar groups attached to a tetrahedral atom, including triisopropylsilyl groups 10,11. The most recent report11 includes results both in solution and the solid state for compound 13 with a TIPS group attached to the 1‐position in naphthalene.…”
Section: Discussionmentioning
confidence: 99%
“…In view of the results in Table 3 for calculated barriers to trimethylstannyl group rotation, it is of interest to know the difference in N ‐TIPS rotation barriers to be expected when the 1‐naphthyl group of 13 is replaced by the N ‐indolyl group of 1 . Calculation of TiPSi rotational barriers is complicated, however, as one torsion usually entrains another 10. We therefore calculated the barrier to a simplified 120° rotation about the peri bond for 13 and for N ‐TIPS‐indole ( 2 ) in the conformation with isopropyl groups ( g , g , g ).…”
Section: Discussionmentioning
confidence: 99%
“…The reaction of alkyldimethylmethoxysilanes with concentrated hydrochloric acid also gave alkyldimethylchlorosilane in high yields. Thus, treatment of i-PrMe 2 SiOMe, sec-BuMe 2 SiOMe, cyclo-HexMe 2 SiOMe, and tert-BuMe 2 SiOMe with 35% aqueous HCl in hydrocarbon at 0°C produced the respective chlorosilanes in quantitative yields, as shown in Table 1 (run [11][12][13][14]. The structures of all chlorosilanes obtained in the present reactions were confirmed by mass and 1 H, 13 C, and 29 Si NMR spectrometric analysis, and spectral data for known compounds were identical with those of the authentic samples.…”
Section: Chlorination Of Dialkylmethyl-and Alkyldimethylalkoxysilanementioning
confidence: 99%
“…78-80°C/10 Torr). All spectral data obtained for i-Pr 3 SiCl are identical with those of the authentic sample reported previously [14].…”
Section: I-pr 3 Siome (Run 1)mentioning
confidence: 99%