1951
DOI: 10.1021/jo01143a005
|View full text |Cite
|
Sign up to set email alerts
|

STUDIES IN SILICO-ORGANIC COMPOUNDS. XIII. ADDITIONAL CHEMICAL PROPERTIES OF TRIALKOXYSILANES1, 2

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
6
0

Year Published

1952
1952
2012
2012

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 12 publications
(7 citation statements)
references
References 7 publications
1
6
0
Order By: Relevance
“…Radical interchange was found to take place between two different silicoorthoesters in 1865 by Friedel and Crafts (8). Analogous reactions may be found, of later date (3)(4)(5).…”
Section: Introductionsupporting
confidence: 54%
“…Radical interchange was found to take place between two different silicoorthoesters in 1865 by Friedel and Crafts (8). Analogous reactions may be found, of later date (3)(4)(5).…”
Section: Introductionsupporting
confidence: 54%
“…During thermal decomposition, the larger number of silanol groups leads to a higher condensation degree and thus, the evolution of the siloxane‐derived species occurs a few degrees later than it occurs in the reference material. Moreover, because of this disproportionation of the TREOS moieties catalyzed by the strong basic conditions, gaseous SiH 4 is formed as a product of the reaction . The evolution of these gaseous species coming from inside the hybrid network could be responsible for the large SSA obtained in these materials.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, because of this disproportionation of the TREOS moieties catalyzed by the strong basic conditions, gaseous SiH 4 is formed as a product of the reaction. 54,55 The evolution of these gaseous species coming from inside the hybrid network could be responsible for the large SSA obtained in these materials.…”
Section: Discussionmentioning
confidence: 99%
“…The formation of the ethoxysilane and the non-formation of the reduction product were confirmed in a larger run (10 g. of silanol) by Dr. G. E. Dunn. Dr. Dunn was also able to show that, when a five-fold excess of anhydrous zinc chloride is used in a reaction lasting 15 minutes, hexaphenyldisiloxane is formed in small amounts; no ethoxysilane could be isolated in this case. When a five-fold excess of zinc chloride was used in a reaction lasting 4 hours, however, neither hexaphenyldisiloxane nor the ethoxysilane could be isolated.…”
Section: Refluxmentioning
confidence: 99%
“…Furthermore, it was shown that tri-o-tolylbenzyloxysilane does not react with methanol under the conditions of the above experiments. Alkoxyl group exchanges have been observed frequently with other types of organosilicon compounds (14,15).…”
mentioning
confidence: 99%