Aix-Marseille Université-CNRS, Institut de Chimie Radicalaire ICR, UMR 7273, 13397, Marseille, France.
J Am Soc Mass Spectrom. 2013 Jul;24(7):1123-9. doi: 10.1007/s13361-013-0665-2. Epub 2013 May 29.
Collision-induced dissociation of doubly charged poly(dimethylsiloxane) (PDMS) molecules was investigated to provide experimental evidence for fragmentation reactions proposed to occur upon activation of singly charged oligomers. This study focuses on two PDMS species holding trimethylsilyl or methoxy end-groups and cationized with ammonium. In both cases, introduction of the additional charge did not induce significant differences in dissociation behavior, and the use of doubly charged precursors enabled the occurrence of charge-separation reactions, allowing molecules always eliminated as neutrals upon activation of singly charged oligomers to be detected as cationized species. In the case of trimethylsilyl-terminated oligomers, random location of the adducted charge combined with rapid consecutive reactions proposed to occur from singly charged precursors could be validated based on MS/MS data of doubly charged oligomers. In the case of methoxy-terminated PDMS, favored interaction of the adducted ammonium with both end-groups, proposed to rationalize the dissociation behavior of singly charged molecules, was also supported by MS/MS data obtained for molecules adducted with two ammonium cations.
采用碰撞诱导解离技术研究了双重荷质比的聚二甲基硅氧烷(PDMS)分子,为单电荷寡聚物发生的碎片化反应提供了实验依据。本研究聚焦于两种带有三甲硅烷基或甲氧基端基并被铵离子化的 PDMS 物质。在这两种情况下,额外电荷的引入并没有引起解离行为的显著差异,并且使用双重荷质比的前体可以发生电荷分离反应,从而可以检测到原本在单电荷寡聚物激活时作为中性物质消除的分子作为被铵离子化的物质。在带有三甲硅烷基端基的寡聚物的情况下,基于双重荷质比寡聚物的 MS/MS 数据可以验证加合电荷的随机位置以及从单电荷前体快速连续反应的假设。对于带有甲氧基端基的 PDMS,加合的铵离子与两个端基的优先相互作用,提出了对单电荷分子解离行为的合理化解释,这也得到了带有两个铵阳离子加合物的分子的 MS/MS 数据的支持。