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Polyurea microcapsules from isocyanatoethyl methacrylate copolymers
Author(s) -
Risangud Nuttapol,
Congdon Thomas R.,
Keddie Daniel J.,
Wilson Paul,
Kempe Kristian,
Haddleton David M.
Publication year - 2016
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/pola.28149
Subject(s) - copolymer , polymer chemistry , methacrylate , isocyanate , polymerization , chemistry , methyl methacrylate , molar mass , polymer , fourier transform infrared spectroscopy , materials science , chemical engineering , organic chemistry , polyurethane , engineering
The synthesis of two types of isocyanate side chain containing copolymers, poly(methyl methacrylate‐ co ‐isocyanatoethyl methacrylate) (P(MMA‐ co ‐IEM)) and poly(benzyl methacrylate‐ co ‐isocyanatoethyl methacrylate) (P(BnMA‐ co ‐IEM)), which were synthesized by Cu(0)‐mediated radical polymerization, is reported. Polymerization proceeded to high conversion giving polymers of relatively narrow molar mass distributions. The incorporation of the bulky aromatic groups in the latter copolymer rendered it sufficiently stable toward hydrolysis and enabled the isolation of the product and its characterization by 1 H and 13 C NMR, and FTIR spectroscopy and SEC. Both P(MMA‐ co ‐IEM) and P(BnMA‐ co ‐IEM) were functionalized with dibutylamine, octylamine, and ( R )‐(+)‐α‐methylbenzyl‐amine, which further proved the successful incorporation of the isocyanate groups. Furthermore, P(BnMA‐ co ‐IEM) was used for the fabrication of liquid core microcapsules via oil‐in‐water interfacial polymerization with diethylenetriamine as crosslinker. The particles obtained were in the size range of 10–90 µm in diameter independent of the composition of copolymer. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 2698–2705

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