New siloxanes with acid-sensitive substituents have been synthesized b
y means of hydrosilylation, starting from methylhydrosiloxanes. Detail
s of the preparation and characterization are reported. p-t-Butoxycarb
onyloxystyrene, p-t-butoxystyrene and t-butyl methacrylate turned out
to be excellent reagents in these experiments. H-1, C-13 and Si-29 nuc
lear magnetic resonance techniques were used for characterization. The
ratio between alpha and beta addition appears to be strongly dependen
t on the substituents at the vinyl group of the organic moieties.