One-pot synthesis of methacrylic acid-ethylene oxide branched block and graft copolymers

Susan Graham, Steve P. Rannard, Peter A.G. Cormack, David C. Sherrington

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Despite the large volume of academic literature on the synthesis and physico-chemical characterization of block copolymers and their potential for application in a wide variety of products, relatively few of these materials have been commercialized. More often than not the main obstacle to this is the high cost of synthesis versus the extra value added to potential products. Devising more cost-effective routes to block copolymers therefore remains an important challenge to polymer chemists. Using conventional solution free radical polymerization we have now synthesized, each in one-pot, architecturally complex ‘branched diblock copolymers’ and compositionally related ‘grafted branched copolymers’, exploiting a generic branching synthetic methodology developed in our own laboratory. In each case blocks of poly(methacrylic acid) and poly(ethylene glycol) (PEG) are involved. The first group was obtained by copolymerization of methacrylic acid with a PEG dimethacrylate with branching favoured in competition with crosslinking by use of appropriate levels of free radical chain transfer agent. For the second series methacrylic acid has been copolymerized with a PEG monomethacrylate and ethylene glycol dimethacrylate, again with crosslinking inhibited by use of a chain transfer agent. Good yields of products are obtained and typically the polymerization mole feed compositions have been chosen to yield an even mass balance of poly(methacrylic acid) and PEG blocks in the copolymers, though this parameter is readily adjustable. The molecular composition of the products has been characterized by elemental microanalysis and 1H NMR spectroscopy, with the latter also combining with multi-angle light scattering size exclusion chromatographic (MALS/SEC) molar mass data to provide information on the branching architecture. The products are complex mixtures in terms of both architecture and molar mass, but the synthetic strategy is far simpler, more practical and more cost-effective than alternative routes to structurally more uniform analogues via multi-step living polymerization procedures are likely to be. The materials are therefore complementary to, rather than competitive with, these analogues. The present approach lends itself to efficient scale-up, and could make significant quantities of materials readily available for further physico-chemical characterization and applications evaluation.
LanguageEnglish
Pages545-552
Number of pages8
JournalJournal of Materials Chemistry
Volume17
Issue number6
Early online date17 Nov 2006
DOIs
Publication statusPublished - 2007

Fingerprint

Ethylene Oxide
Graft copolymers
Polyethylene glycols
Block copolymers
Ethylene
Oxides
Acids
Molar mass
Crosslinking
Copolymers
Costs
Living polymerization
Microanalysis
Free radical polymerization
Complex Mixtures
Chemical analysis
Light scattering
Copolymerization
Nuclear magnetic resonance spectroscopy
Free Radicals

Keywords

  • one-pot synthesis
  • methacrylic acid–ethylene oxide
  • copolymers

Cite this

Graham, Susan ; Rannard, Steve P. ; Cormack, Peter A.G. ; Sherrington, David C. / One-pot synthesis of methacrylic acid-ethylene oxide branched block and graft copolymers. In: Journal of Materials Chemistry. 2007 ; Vol. 17, No. 6. pp. 545-552.
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One-pot synthesis of methacrylic acid-ethylene oxide branched block and graft copolymers. / Graham, Susan; Rannard, Steve P.; Cormack, Peter A.G.; Sherrington, David C.

In: Journal of Materials Chemistry, Vol. 17, No. 6, 2007, p. 545-552.

Research output: Contribution to journalArticle

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T1 - One-pot synthesis of methacrylic acid-ethylene oxide branched block and graft copolymers

AU - Graham, Susan

AU - Rannard, Steve P.

AU - Cormack, Peter A.G.

AU - Sherrington, David C.

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KW - one-pot synthesis

KW - methacrylic acid–ethylene oxide

KW - copolymers

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VL - 17

SP - 545

EP - 552

JO - Journal of Materials Chemistry

T2 - Journal of Materials Chemistry

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