Abstract
Phosphazene-substituted polysiloxanes have been synthesized via a hydrosilylation reaction of allyl derivatives of cyclophosphazenes with polymethylhydrosiloxanes. It turned out that a proper choice of both the spacer between the phosphazene group and the double bond and the position of the phosphazene group at the spacer is important for the preparation of soluble polysiloxanes with a high content of phosphazene units.
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