化学
碎片(计算)
亚苯基
硫化物
离子
聚合物
质谱法
高分子化学
有机化学
色谱法
计算机科学
操作系统
作者
Anthony P. Gies,Jon F. Geibel,David M. Hercules
出处
期刊:Macromolecules
[American Chemical Society]
日期:2009-12-04
卷期号:43 (2): 952-967
被引量:21
摘要
A study involving the evaporation−grinding MALDI sample preparation method, MALDI-TOF/TOF CID, and Py-GC/MS is presented to examine the fragmentation mechanisms of poly(p-phenylene sulfide) (PPS). MALDI-TOF/TOF CID fragmentation studies yielded a wealth of information about the mass, structure (linear or cyclic), end-groups, and backbone modifications of the polymer. Additionally, Py-GC/MS experimental data are presented for comparison of the multimolecular free radical reactions in pyrolysis with the unimolecular fragmentation reactions of MS/MS.(1, 2) TOF/TOF CID results indicate that linear PPS undergoes random main chain fragmentation along the polymer backbone and preferentially fragments at bonds adjacent to dibenzothiophene and phenyl end-groups. Cyclic species produce fragment ions similar to linear species. However, the MS/MS precursor ions for cyclic PPS are, by far, the most intense peaks, while the precursor ions for linear species show relatively low intensity. CID fragmentation results are supported by Py-GC/MS data and are consistent with the proposed degradation mechanisms.
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