Tandem mass spectrometry characteristics of polyester anions and cations formed by electrospray ionization

被引:29
作者
Arnould, MA
Vargas, R
Buehner, RW
Wesdemiotis, C [1 ]
机构
[1] Univ Akron, Dept Chem, Akron, OH 44325 USA
[2] UCB Chem Corp, Smyrna, GA 30080 USA
关键词
polyester; copolymer; MALDI; ESI; MS/MS; end groups; monomer sequence; fragmentation;
D O I
10.1255/ejms.746
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Electrospray ionization of polyesters composed of isophthalic acid and neopentyl glycol produces carboxylate anions in negative mode and mainly sodium ion adducts in positive mode. A tandem mass spectrometry (MS/MS) study of these ions in a quadrupole ion trap shows that the collisionally-activated dissociation pathways of the anions are simpler than those of the corresponding cations. Charge-remote fragmentations predominate in both cases, but the spectra obtained in negative mode are devoid of the complicating cation exchange observed in positive mode. MS/MS of the Na+ adducts gives rise to a greater number of fragments but not necessarily more structural information. In either positive or negative mode, polyester oligomers with different end groups fragment by similar mechanisms. The observed fragments are consistent with rearrangements initiated by the end groups. Single-stage ESI mass spectra are also more complex in positive mode because of extensive H/Na substitutions; this is also true for matrix-assisted laser desorption ionization mass spectra. Hence, formation and analysis of anions might be the method of choice for determining block length, end group structure and copolymer sequence, provided the polyester contains at least one carboxylic acid end group that is ionizable to anions.
引用
收藏
页码:243 / 256
页数:14
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