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HERO ID
4280125
Reference Type
Journal Article
Title
Quantitative omega-amination, omega-azidolysis, and omega-thiolation of poly(ethylene oxide)s through anionic mechanism
Author(s)
Kim, SWoo; Siddique, AbuB; An, JinW; Park, HJ; Kim, HJun; Kang, HoJ; Lee, JaeY; Kim, S; Kim, J
Year
2016
Is Peer Reviewed?
1
Journal
Macromolecular Research
ISSN:
1598-5032
Volume
24
Issue
2
Page Numbers
188-195
DOI
10.1007/s13233-016-4023-7
Web of Science Id
WOS:000371255900013
Abstract
n-Butyllithium-initiated ring-opening polymerization of ethylene oxide with potassium t-butoxide in the mixture of benzene and dimethyl sulfoxide (DMSO) at 35 A degrees C yielded corresponding "living" polymeric alkoxide. The molecular weight was well controlled on the basis of stoichiometric balance. Quantitative chain-end functionalizations, such as the amination, the azidation, and the thiolation of polymeric alkoxide, were performed. The yields were almost quantitative (over 98 mol%). The resulting products were characterized by the combination of H-1 NMR spectroscopy, UV/Visible spectroscopy, FTIR, MALDI-TOF MS analysis, and size exclusion chromatographic analysis.
Keywords
poly(ethylene oxide); molecular weight control; chain-end functionalizations; amination; azidation; thiolation
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