Title
A silicon-29 NMR study of adduct formation in organosilanes
Document Type
Article
Publication Title
Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry
Publication Date
1-1-2003
Abstract
The reactions of a series of methyl-and phenylsilanes containing one or more electronegative groups such as chloro, triflate (OTf), trifluoroacetate, and trifluoroethoxy with the base HMPA were investigated with 29Si NMR and conductivity titrations in both methylene chloride and acetonitrile solvents. Formation of both five-coordinate adduct and four-coordinate electrolyte (such as Me3Si(HMPA) +OTf-) was observed for some of the strongly electron attracting groups, whereas only adduct formation was observed for the chloro group. Electrolyte formation is also favored by an increase in the base to acid mole ratio and the more polar acetonitrile. The effect of the Si - H bond on the Lewis acidity of organosilanes in intermolecular adduct formation was documented and is believed to be a result of bond strengthening steric effect.
Volume
33
Issue
3
First Page
359
Last Page
367
DOI
10.1081/SIM-120019990
ISSN
00945714
Recommended Citation
Margolis, Lara A.; Schaeffer, Charles D.; and Yoder, Claude H., "A silicon-29 NMR study of adduct formation in organosilanes" (2003). Faculty Publications. 1467.
https://jayscholar.etown.edu/facpubharvest/1467