Curtin University Homepage
  • Library
  • Help
    • Admin

    espace - Curtin’s institutional repository

    JavaScript is disabled for your browser. Some features of this site may not work without it.
    View Item 
    • espace Home
    • espace
    • Curtin Research Publications
    • View Item
    • espace Home
    • espace
    • Curtin Research Publications
    • View Item

    Composing Well-Defined Stimulus-Responsive Materials Through Postpolymerization Modification Reactions

    227048_227048a.pdf (1.155Mb)
    Access Status
    Open access
    Authors
    Roth, Peter
    Date
    2014
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Roth, P. 2014. Composing Well-Defined Stimulus-Responsive Materials Through Postpolymerization Modification Reactions. Macromolecular Chemistry and Physics. 215 (9): pp. 825-838.
    Source Title
    Macromolecular Chemistry and Physics
    DOI
    10.1002/macp.201400073
    ISSN
    1022-1352
    Remarks

    This is the peer reviewed version of the following article: Roth, P. 2014. Composing Well-Defined Stimulus-Responsive Materials Through Postpolymerization Modification Reactions. Macromolecular Chemistry and Physics. 215 (9): pp. 825-838, which has been published in final form at http://doi.org/10.1002/macp.201400073. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving at http://olabout.wiley.com/WileyCDA/Section/id-820227.html#terms

    URI
    http://hdl.handle.net/20.500.11937/31971
    Collection
    • Curtin Research Publications
    Abstract

    Postpolymerization modification—the installation of functional groups into a premade, reactive polymeric precursor—is emerging as an advantageous synthetic strategy toward tailored materials. In this article, the preparation of environmentally sensitive, “smart,” polymers by virtue of postpolymerization modification is presented. The underlying fundamentals of different types of stimulus-responsiveness are highlighted with an emphasis on thermo­responsiveness, encompassing lower and upper critical solution temperature (LCST and UCST) behavior. Using a range of postpolymerization modifications as examples, properties imparted through incorporation of specific functional groups and their structure–property relations are discussed. Strategies for an appropriate choice of functionality in order to obtain well-defined materials with custom-made behavior are presented.

    Related items

    Showing items related by title, author, creator and subject.

    • The synthesis and aqueous solution properties of sulfobutylbetaine (co)polymers: comparison of synthetic routes and tuneable upper critical solution temperatures
      Zhu, Y.; Noy, J.; Lowe, Andrew; Roth, P. (2015)
      Polysulfobutylbetaine (SBB) (co)polymers, zwitterionic species bearing ammonium and sulfonate groups separated by a butyl spacer in every repeat unit, were prepared through three different synthetic routes and their aqueous ...
    • Thiol-Michael coupling chemistry: Facile access to a library of functional exo-7-oxanorbornenes and their ring-opening metathesis (co)polymerization
      Liu, M.; Van Hensbergen, J.; Burford, R.; Lowe, Andrew (2012)
      The nucleophile initiated thiol-Michael reaction of a wide range of mono and multifunctional thiols with a novel acrylic exo-7-oxanorbornene is described. We highlight how this process affords ready access to a large ...
    • Hydrophobically Modified Sulfobetaine Copolymers with Tunable Aqueous UCST through Postpolymerization Modification of Poly(pentafluorophenyl acrylate)
      Woodfield, P.; Zhu, Y.; Pei, Y.; Roth, Peter (2014)
      Polysulfobetaines, polymers carrying highly polar zwitterionic side chains, present a promising research field by virtue of their antifouling properties, hemocompatibility, and stimulus-responsive behavior. However, limited ...
    Advanced search

    Browse

    Communities & CollectionsIssue DateAuthorTitleSubjectDocument TypeThis CollectionIssue DateAuthorTitleSubjectDocument Type

    My Account

    Admin

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    Follow Curtin

    • 
    • 
    • 
    • 
    • 

    CRICOS Provider Code: 00301JABN: 99 143 842 569TEQSA: PRV12158

    Copyright | Disclaimer | Privacy statement | Accessibility

    Curtin would like to pay respect to the Aboriginal and Torres Strait Islander members of our community by acknowledging the traditional owners of the land on which the Perth campus is located, the Whadjuk people of the Nyungar Nation; and on our Kalgoorlie campus, the Wongutha people of the North-Eastern Goldfields.