Building on results from our previous study of 2-ring methylenedianiline (MDA), a combined mass spectrometry approach utilizing ion mobility-mass spectrometry (IM-MS) and tandem mass spectrometry (MS/MS) coupled with computational methods enables the structural characterization of purified 3-ring and 4-ring MDA regioisomers in this current study. The preferred site of protonation for the 3-ring and 4-ring MDA was determined to be on the amino groups. Additionally, the location of the protonated amine along the MDA multimer was found to influence the gas phase stability of these molecules. Fragmentation mechanisms similar to the 2-ring MDA species were observed for both the 3-ring and 4-ring MDA. The structural characterization of 3-ring and 4-ring MDA isomers using modern MS techniques may aid polyurethane synthesis by the characterization of industrial grade MDA, multimeric MDA species, and methylene diphenyl diisocyanate (MDI) mixtures.

•First MALDI collision-induced dissociation study of wholly aromatic polyesters.•Effect of polymer end groups and bond energies on collision-induced mass spectra.•Effect of end groups on polymer fragmentation mechanisms.•Fragmentation mechanisms compared to those for aliphatic polyesters and aramids.•Both charge-site and charge-remote fragmentation reactions observed.MALDI-TOF/TOF collision-induced dissociation (CID) experiments were conducted on model aromatic polyester oligomers. CID fragmentation studies identified initial fracture of the ester bond and subsequent CO loss as a major pathway, consistent with the general fragmentation mechanism used to explain the origin of poly(p-phenylenediamine terephthalamide) (PPD-T) fragment ions. Specifically, both charge-remote and charge-site fragmentation were observed. Different parent-ion species were observed, the major ones being carboxyl-hydroxyl, di-carboxyl, di-hydroxyl, and phenyl-carboxyl terminated. One species observed was hydroxyl-diethylamine terminated caused by reaction of carboxyl groups with triethylamine added to the synthesis reaction mixture. Fragment ions reflected the end groups of the parent oligomers. Some MALDI fragment-ion spectra were obtained for species showing exchange between Li and H at the carboxyl end group. Bond energy calculations provide further insight into suggested fragmentation mechanisms.

Purified methylenedianiline (MDA) regioisomers were structurally characterized and differentiated using tandem mass spectrometry (MS/MS), ion mobility-mass spectrometry (IM-MS), and IM-MS/MS in conjunction with computational methods. It was determined that protonation sites on the isomers can vary depending on the position of amino groups, and the resulting protonation sites play a role in the gas-phase stability of the isomer. We also observed differences in the relative distributions of protonated conformations depending on experimental conditions and instrumentation, which is consistent with previous studies on aniline in the gas phase. This work demonstrates the utility of a multifaceted approach for the study of isobaric species and elucidates why previous MDA studies may have been unable to detect and/or differentiate certain isomers. Such analysis may prove useful in the characterization of larger MDA multimeric species, industrial MDA mixtures, and methylene diphenyl diisocyanate (MDI) mixtures used in polyurethane synthesis.

•This represents the first derailed MS/MS study of aramid polymers.•MALDI-TOF/TOF collision-induced dissociation experiments are reported on model PPD-T polymers.•Diamine-terminated oligomers were the major product of synthesis using excess amine.•Di-carboxylic acid oligomers were the major product for excess acid.MALDI-TOF/TOF collision-induced dissociation (CID) experiments are reported on model poly(p-phenylenediamine terephthalamide) (PPD-T) polymers, revealing a variety of synthesis reaction products. Diamine-terminated oligomers were the major product of synthesis using excess amine, and di-carboxylic acid oligomers were the major product for excess acid. Structures of major reaction products were confirmed by CID fragmentation studies, along with detailed studies of MS/MS decomposition pathways. Apparent fracture of the phenylcarbonyl bond was the major fragmentation pathway (independent of end groups), resulting from initial NHCO bond cleavage with subsequent CO loss. Hydrogen-transfer reactions play an important role in fragmentation, involving both cross-chain abstraction of NH hydrogen and long-range H-transfer. End-group and main-chain modifications produce fingerprint CID fragmentation patterns that can be used to identify end groups and branching patterns; the structure of an unanticipated synthesis product was established using CID. The effect of synthesis conditions on polymer composition was studied using the analysis of variance, specifically, the amine-to-acid ratio used and post-synthesis addition of CaO. Of particular interest is oligomer end-group modification by the solvent (N-methyl pyrrolidone) induced by addition of CaO.