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The chemical modification of poly(vinyl alcohol) (PVA) was performed through oxidation followed by nucleophilic addition. PVA was oxidized by KMnO4 to form vinyl ketone units along the polymer backbone. The chemical modification of PVA was then conducted through the reaction of the carbonyl group of the vinyl ketone unit with 9,10‐dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxide (DOPO) as a nucleophile. Through this approach, the phosphorous DOPO group was attached onto the carbon atom of the polymer main chain rather than onto the pendent hydroxyl groups of PVA. The formed DOPO‐containing PVA showed improved thermal stability, organosolubility, and flame retardance. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1107–1113, 2003

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Polyaryloxydiphenylsilanes were prepared from phosphorus-containing diols and diphenydichlorolsilane through solution polymerization. With a stoichiometric imbalance in feed monomers, the resulting polymers exhibited moderate melting points and good processing properties. The polymers prepared showed initial decomposition temperatures above 340°C, excellent thermal stability, high char yields at 850°C and very high limited oxygen index values of 56-59. The polymers' char yields and their (P þ Si) contents showed linear relationships.

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