Hydrosilylation reactions have been used to functionalise the exterior surf
aces of octavinyloctasilsesquioxane molecules to provide routes to octaalde
hyde molecules. These have been characterised by NMR and MALDI (matrix assi
sted laser desorption/ionisation)-TOF mass spectroscopy. Further reactions
of the molecules to produce carboxylic acid and Schiff base functionalised
species are also reported. The effect of temperature and catalyst on the re
gioselectivity of the reaction is discussed.