Trapping reactions, matrix isolation and kinetics of a few photogenerated silylenes and silenes have been studied. Several vinylsiliranes, the long sought intermediates from the addition of dimesitylsilylene to various 1,3-dienes, have been made and characterized. The product study by various nmr techniques demonstrates that the silylene addition to the dienes is highly stereospecific and the addition to the cis v bond is about 9 times faster than to the trans one in gis,trans-2,4-hexadiene. High stereospecifity of the addition of dimesitylsilylene to cis and trans-2-pentenes and to cis and trans-4-octenes has also been found. The reinvestigation of dimesitylsilylene to cis and t;rans-2-butene affords the possible explanation for the confusing results and wrong conclusion from the earlier report by Ando and coworkers.
| Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc332838 |
| Date | 08 1900 |
| Creators | Zhang, Shizhong |
| Publisher | University of North Texas |
| Source Sets | University of North Texas |
| Language | English |
| Detected Language | English |
| Type | Thesis or Dissertation |
| Format | v, 143 leaves : ill., Text |
| Rights | Public, Zhang, Shizhong, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved. |
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