Tandem mass spectrometry of low solubility polyamides

The structural characterization of polyamides (PA) was achieved by tandem mass spectrometry (MS/MS) with a laser induced dissociation (LID) strategy. Because of interferences for precursor ions selection, two chemical modifications of the polymer end groups were proposed as derivatization strategies. The first approach, based on the addition of a trifluoroacetic acid (TFA) molecule, yields principally to complementary b_n and y_n product ions. This fragmentation types, analogous to those obtained with peptides or other PA, give only poor characterization of polymer end-groups 1]. A second approach, based on the addition of a basic diethylamine (DEA), permits to fix the charge and favorably direct the fragmentation. In this case, b_n ions were not observed. The full characterization of ω end group structure was obtained, in addition to the expected y_n and consecutive fragment ions.