The synthetic studies include the synthesis of the cyclic siloxydiyne, 3,3,5,5,8,8,10,10-octamethyl-4,9-dioxa-3,5,8,10-tetrasilacyclodeca-1,6- diyne [VI] and its novel iron carbonyl complex. In the preparation of [VI] by HBr promoted condensation of bis (methoxydimethylsilyl) acetylene, a minor product, a cyclic trimer was always formed along with the major product [VI]. No evidence of an equilibrium between the trimerization product and the dimerization product was found. Compound [VI] can react with iron carbonyl reagents to produce a novel binuclear iron complex of trimethylenemethane [VII] in very low yield either in a thermal or photo-reaction. The key step proposed by us in the formation of [VII] is a I,2-silyl shift in a complexed bis (silyl) acetylene to form a vinylidene intermediate. Experiments aimed at isolating this intermediate were not successful.
| Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc500871 |
| Date | 12 1900 |
| Creators | Chi, Xiang-yong |
| Contributors | Jones, Paul R., Thomas, Ruthanne D. |
| Publisher | University of North Texas |
| Source Sets | University of North Texas |
| Language | English |
| Detected Language | English |
| Type | Thesis or Dissertation |
| Format | v, 41 leaves : ill., Text |
| Rights | Public, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved., Chi, Xiang-yong |
Page generated in 0.0024 seconds