A soluble poly(phenylene sulfide) (PPS) derivative was synthesized by oxidative polymerization of bis(3,5-dimethylphenyl) disulfide. The obtained poly(thio-2,6-dimethyl-1,4-phenylene) (I) (M̄w = 22900, M̄n = 8400) was brominated by the reaction with N-bromosuccinimide (NBS). The bromomethyl substituents on PPS are reactive and were converted quantitatively to hydroxymethyl groups by hydrolysis in NMP at 100°C. The reaction of the bromomethylated PPS with tertiary amines gave the quaternized polymer, which is stable up to 145°C in the solid state and in refluxing methanol.
|ジャーナル||Macromolecular Chemistry and Physics|
|出版ステータス||Published - 1999 8月|
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