This investigation is concerned with determining whether a carbon substituent or a silicon substituent on the carbon terminus of a silicon-carbon double bond has a more stabilizing effect. Two different 2-substituted silaethylenes were generated at the same time by pyrolyzing 1, 1-dimethyl-2-neopentyl-4- (dimethylalkoxysilyl) silacyclobutanes in a nitrogen flow system. The results of these pyrolyses, both neat and in the presence of a trapping reagent, show that the silaethylene with a silicon substituent on the carbon terminus was favored approximately two to one over the silaethylene with a carbon substituent. This datum, along with other observations and hypotheses discussed, leads to the suggestion that the silicon substituenton the carbon terminus of the silaethylene bond has a more stabilizing effect than the carbon substituent.
| Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc504095 |
| Date | 12 1900 |
| Creators | Snyder, Walter David |
| Contributors | Jones, Paul R., Theriot, L. J. |
| Publisher | North Texas State University |
| Source Sets | University of North Texas |
| Language | English |
| Detected Language | English |
| Type | Thesis or Dissertation |
| Format | iv, 51 leaves: ill., Text |
| Rights | Public, Snyder, Walter David, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved. |
Page generated in 0.0023 seconds