The mass spectral characteristics of poly(2,6‐dimethyl‐1,4‐phenylene ether), its monomer (2,6‐xylenol), and its dimer (3,5‐dimethyl‐4‐hydroxyphenyl 2,6‐xylyl ether) have been determined. The monomer and dimer show peaks for the molecular ions (122; 242 amu) and degradation patterns similar to those of o ‐methylaryl ethers. Loss of methyl and cleavage of the ether with transfer of an o ‐methyl hydrogen are observed. Metastable transitions are recorded corresponding to a loss of 15 from 122 and 56 from 107 amu (xylenol) and of 151 from 242 and 40 from 104 amu (ether). The polymer volatilizes readily at 380–400°C. (TGA shows rapid weight loss at 400°C) and gives sets of peaks at ( N × 120) ± 14 up to 1080 ( N = 9). The principal peak is at ( N × 120) + 2, calibrated against PFA, and this is attributed to an ion of a volatilized oligomer. The oligomer is either present as such, is formed in a degradation process involving an ether redistribution, or is formed in a hydrogen transfer process in the ether cleavage reaction.
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Richard H. Wiley (1971) studied this question.
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