Abstract

The mass spectra of dimeric degradation products of poly(2,6-dimethyl-1,4-phenylene oxide) are discussed. It has been found that the main fragmentation mechanism of rearranged dimer is β-benzyl cleavage giving rise to odd-mass ions and ortho hydroxyl hydrogen transfer yielding even-mass ions. The mass spectra of unrearranged dimers are very similar though it could not be concluded that Fries-type rearrangement takes place on electron impact.

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