[1 + 4]-Cycloaddition of a stable silylene to 2,4,6-tri-tert-butyl-1,3,5-triphosphabenzene

1999 ◽  
pp. 2451-2452 ◽  
Author(s):  
Scott B. Clendenning ◽  
Barbara Gehrhus ◽  
Peter B. Hitchcock ◽  
John F. Nixon
Keyword(s):  

2000 ◽  
Vol 78 (11) ◽  
pp. 1526-1533 ◽  
Author(s):  
Michael Haaf ◽  
Thomas A Schmedake ◽  
Bryan J Paradise ◽  
Robert West

The synthesis and several reactions of the stable silylene 1 (N,N'-di-tert-butyl-1,3-diaza-2-sila-2-ylidene) are reported. Overreduction of 1 with alkali metals results in the formation of a dimeric dianion, which can be trapped with a proton source to give the dihydride derivative 9. In the solid state or in concentrated solutions, 1 undergoes a reversible conversion into the novel tetrameric disilene, 10. 1 reacts with ethanol, phenol, and water via insertion into the O—H bond, and with iodomethane by insertion into the C—I bond. A reaction of 1 with the diene 2,3-dimethyl-1,3-butadiene affords the silacyclopentene, 15. This reaction is markedly different from the one found for the unsaturated analog of the silylene, 2, which catalyzes the conversion of this diene into a highly cross-linked polymer.Key words: silylene, carbene analog, disilene, divalent compounds, N-heterocycles.





1990 ◽  
Vol 80 (2) ◽  
pp. 226-232
Author(s):  
Tomoaki Matsuo ◽  
Yumiko Kashiwaki ◽  
Saburo Itoo


1995 ◽  
Vol 210 (3) ◽  
pp. 224-224 ◽  
Author(s):  
F. Knoch ◽  
R. Appel ◽  
H. Wenzel
Keyword(s):  








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