GRAPHICAL ABSTRACT
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Abstract
The sodium dithionite–initiated reaction of perfluoroalkyl iodides with vinylsiloxane in an acetonitrile–water mixture efficiently proceeded under mild conditions. As a result, the perfluoroalkyl groups were bonded onto C˭C on the end-position or side-chain of the siloxane. The subsequent elimination or reduction of the C‒I bridged groups produced the corresponding RfCH˭CH‒ or RfCH2CH2− substituted group on siloxane. All fluorosiloxanes were characterized by FT-IR, 1H NMR, 19F NMR, and EI-MS. The morphology and microstructures of the fluorosiloxane films were further observed by atomic force microscopy and X-ray photoelectron microscope.