Catalytic trimerization of isocyanates by neutral pentacoordinated silicon hydrides
✍ Scribed by Robert J. P. Corriu; Gérard F. Lanneau; Vimal D. Mehta
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 244 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
Pentacoordinated hydrosilanes react with excess of aryl isocyanates to give isocyanurates under mild and neutral conditions. The catalytic species are the initially formed N-silylfi~rmamides, which incorporate three equivalents of isocyanate, and then rearrange to N-silylformamide and isocyanurates.
📜 SIMILAR VOLUMES
Five different ligands attached to a single silicon atom are found in the pentacoordinate silicon(IV) complexes with SiClSONC and SiISONC skeletons (see picture). R. Tacke and co-workers describe in their Communication on page 7006 ff. the synthesis and structural analysis of both complexes, which e
The hydrogenated silicon carbides SiC,H' ( ) are generated and characterized in the gas phase by neutralization-reionization mass spectrometry. The mass spectra are in keeping with a linear connectivity SiC,W and rule out the isomeric form HSiC;.