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Silanimine. isomerization

The model silylnitrene-silanimine isomerization (H3SiN- H2Si=NH) was stud-... [Pg.137]

The thus formed heterocycles 412a decompose or isomerize thermally the required reaction temperature depends on the substituents. The isomerization leads to diazomethane derivatives 413a, whereas the decomposition by [2 + 3] cycloreversion reaction gives bis(trimethylsilyl)diazomethane and short-lived silanimines 414a, which dimerize in most cases. The ratio isomerization/cycloreversion depends on R, the solvent and the temperature and more cycloreversion is observed at higher temperature. An unfavourable side reaction is the insertion of Me2Si=NR into Si—N bonds (formation of 415a and 686 see below). [Pg.1012]


See other pages where Silanimine. isomerization is mentioned: [Pg.221]    [Pg.668]    [Pg.1021]    [Pg.1158]    [Pg.1159]    [Pg.8]    [Pg.137]    [Pg.139]    [Pg.1021]    [Pg.1158]   
See also in sourсe #XX -- [ Pg.668 ]




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