This article reports on the chemical functionalization of hydrogen-terminated porous silicon (PSi−H) nanostructures with alkenes, aldehydes, and alkyl halides under microwave irradiation. The technique allows for the introduction of different functional groups on the surface. The use of microwave irradiation has a net effect on the hydrosilylation reaction rate. However, no specific microwave effect was observed when the freshly prepared PSi−H surface was modified with an alkene bearing an aldehyde function. The reaction takes place at both the carbon−carbon and the carbon−oxygen double bonds. The polar aldehyde functional group did not show a dominant effect in directing the reaction selectively at the carbonyl group.
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Petit et al. (2008) studied this question.
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