Characterization of Different Poly(2-oxazoline) Block Copolymers by MALDI-TOF MS/MS and ESI-Q-TOF MS/MS

被引:27
作者
Baumgaertel, Anja [1 ,2 ]
Altuntas, Esra [1 ,2 ]
Kempe, Kristian [1 ]
Crecelius, Anna [1 ,2 ]
Schubert, Ulrich S. [1 ,2 ]
机构
[1] Univ Jena, Lab Organ & Macromol Chem IOMC, D-07743 Jena, Germany
[2] Dutch Polymer Inst, NL-5612 AB Eindhoven, Netherlands
关键词
block copolymers; ESI; MALDI; poly(2-oxazoline); mass spectrometry; RING-OPENING POLYMERIZATION; MICROWAVE-ASSISTED POLYMERIZATION; CYCLIC IMINO ETHERS; MASS-SPECTROMETRY; FLUORINATED; 2-PHENYL-2-OXAZOLINES; DISTRIBUTIONS; 2-OXAZOLINES; IONIZATION; CHEMISTRY; POLYMERS;
D O I
10.1002/pola.24364
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A complete library of poly(2-oxazoline) block copolymers was synthesized via cationic ring opening polymerization for the characterization by two different soft ionization techniques, namely matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) and electrospray ionization quadrupole time-of-flight mass spectrometry (ESI-Q-TOF MS). In addition, a detailed characterization was performed by tandem MS to gain more structural information about the block copolymer composition and its fragmentation behavior. The fragmentation of the poly(2-oxazoline) block copolymers revealed the desired polymer structure and possible side reactions, which could be explained by different mechanisms, like 1,4-ethylene or hydrogen elimination and the McLafferty +1 rearrangement. Polymers with aryl side groups showed less fragmentation due to their higher stability compared to polymers with alkyl side groups. These insights represent a further step toward the construction of a library with fragments and their fragmentation pathways for synthetic polymers, following the successful examples in proteomics. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 5533-5540, 2010
引用
收藏
页码:5533 / 5540
页数:8
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