Mass spectrometry and ion mobility study of poly(ethylene glycol)‐based polyurethane oligomers
Autor: | Jody C. May, Ian D. Tomlinson, Berkley M. Ellis, David M. Hercules, John A. McLean, Rachel A. Harris, Jaqueline A. Picache, Emanuel Zlibut |
---|---|
Rok vydání: | 2020 |
Předmět: |
chemistry.chemical_classification
Chemistry Ion-mobility spectrometry 010401 analytical chemistry Organic Chemistry Polymer Mass spectrometry Tandem mass spectrometry 01 natural sciences Oligomer 0104 chemical sciences Analytical Chemistry chemistry.chemical_compound Polymerization Polymer chemistry Copolymer Ethylene glycol Spectroscopy |
Zdroj: | Rapid Communications in Mass Spectrometry. 34 |
ISSN: | 1097-0231 0951-4198 |
Popis: | RATIONALE Commercial-grade polymer synthesis is performed via melt polymerization, which leads to polydispersion. The work reported herein provides a synthetic strategy to produce mono-dispersive polyurethane oligomers and an analytical strategy to distinguish these oligomers, providing chemists with the tools necessary to synthesize and identify specific polymer structures that exhibit a desired property. METHODS Three isomeric poly(ethylene glycol)-polyurethane (PEG-PUR) oligomers were synthesized and analyzed via flow-injection ion mobility mass spectrometry (IM-MS). Each polymer oligomer was injected and run independently via flow injection at 100 μL•min-1 and analyzed in positive ion mode on a drift tube quadrupole time-of-flight (QTOF) instrument. Mobility measurements were determined using a single-field approach. For tandem mass spectrometry (MS/MS) experiments, the sodium-adducted singly charged precursor ion was isolated in the quadrupole and subjected to a range of collision energies. RESULTS In MS experiments, both +1 and +2 sodium-adducted species were observed for each oligomer at m/z 837.4 and 430.2, respectively. When isolated and fragmented via MS/MS, the +1 precursor yielded distinct product ions for each of the three isomeric oligomers. Fragmentation generally occurred at urethane linkages via 1,3- and 1,5-H shift mechanisms. IM was also used to distinguish the three isomers, with greater IM separation observed for the +2 versus the +1 species. CONCLUSIONS Mono-disperse PEG-PUR oligomers were synthesized and analyzed. Although the polymeric oligomers analyzed in this study are quite small and structurally simple, this work serves as a model system for the synthesis and structural characterization of larger, more complex block copolymers. |
Databáze: | OpenAIRE |
Externí odkaz: |