The sulphur(<scp>II</scp>)–nitrogen bond. Part II. The transamination of diamino sulphides and sulphenamides
作者:D. A. Armitage、M. J. Clark、A. M. White
DOI:10.1039/j39710003141
日期:——
The application of transamination to diaminosulphides and to benzene- and methane-sulphenamides gives high yields of sulphur(II) nitrogen compounds. The mixtures resulting from secondary amines and methanesulphenyl chloride can be conveniently separated by use of this reaction. Transamination of gem-diamines has been observed.
Organoaminosilanes, such as without limitation di-iso-propylaminosilane (DIPAS), are precursors for the deposition of silicon containing films such as silicon-oxide and silicon-nitride films. Described herein are methods to make organoaminosilane compounds, or other compounds such as organoaminodisilanes and organoaminocarbosilanes, via the catalytic hydrosilylation of an imine by a silicon source comprising a hydridosilane.