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Novel Michael Addition Networks Containing Poly(propylene glycol) Telechelic Oligomers
Author(s) -
Mather Brian D.,
Miller Kevin M.,
Long Timothy E.
Publication year - 2006
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.200600167
Subject(s) - polymer chemistry , monomer , ethyl acetoacetate , michael reaction , catalysis , polyvinyl alcohol , chemistry , polymer , copolymer , molar mass distribution , materials science , organic chemistry
Summary: Poly(propylene glycol) oligomers with molecular weights ranging from 1 000 to 8 000 g · mol −1 were end‐functionalized with acetoacetate groups and subsequently crosslinked using carbon‐Michael addition with PEG diacrylate. Gel fraction analysis, DMA, TGA, tensile, and swelling measurements were utilized to characterize the networks. The thermomechanical properties of the networks were analyzed with respect to the molecular weight between crosslink points ( M c ) and the critical molecular weight for entanglement ( M e ). Sampling experiments during crosslinking revealed the evolution of molecular weight with time and monomer conversion. Kinetic analyses of the Michael additions were performed using 1 H NMR spectroscopy, and the influence of basic catalyst and concentration was elucidated.Synthesis of acetoacetate networks from acetoacetate‐functionalized PPG using DBU as a basic catalyst.

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