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    Thermoresponsive Poly(2-oxazoline) Molecular Brushes by Living Ionic Polymerization: Kinetic Investigations of Pendant Chain Grafting and Cloud Point Modulation by Backbone and Side Chain Length Variation

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    Type
    Article
    Authors
    Zhang, Ning
    Luxenhofer, Robert
    Jordan, Rainer
    Date
    2012-04-17
    Online Publication Date
    2012-04-17
    Print Publication Date
    2012-05-14
    Permanent link to this record
    http://hdl.handle.net/10754/600004
    
    Metadata
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    Abstract
    Molecular brushes of poly(2-oxazoline)s were prepared by living anionic polymerization of 2-iso-propenyl-2-oxazoline to form the backbone and subsequent living cationic ring-opening polymerization of 2-n- or 2-iso-propyl-2-oxazoline for pendant chain grafting. In situ kinetic studies indicate that the initiation efficiency and polymerization rates are independent from the number of initiator functions per initiator molecule. This was attributed to the high efficiency of oxazolinium salt and the stretched conformation of the backbone, which is caused by the electrostatic repulsion of the oxazolinium moieties along the macroinitiator. The resulting molecular brushes showed thermoresponsive properties, that is, having a defined cloud point (CP). The dependence of the CP as a function of backbone and side chain length as well as concentration was studied. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
    Citation
    Zhang N, Luxenhofer R, Jordan R (2012) Thermoresponsive Poly(2-oxazoline) Molecular Brushes by Living Ionic Polymerization: Kinetic Investigations of Pendant Chain Grafting and Cloud Point Modulation by Backbone and Side Chain Length Variation. Macromolecular Chemistry and Physics 213: 973–981. Available: http://dx.doi.org/10.1002/macp.201200015.
    Sponsors
    This work was supported by the Elitenetzwerk Bayern in the frame of the international graduate school CompInt ("Materials Science of Complex Interfaces") as part of the IGSSE ("International Graduate School for Science and Engineering") at the Technische Universitat Munchen. R.J. thanks for additional support by the Cluster of excellence "Center for Regenerative Therapies Dresden" (CRTD). R. L. was supported by a postdoctoral stipend from the King Abdullah University of Science and Technology (KAUST).
    Publisher
    Wiley
    Journal
    Macromolecular Chemistry and Physics
    DOI
    10.1002/macp.201200015
    ae974a485f413a2113503eed53cd6c53
    10.1002/macp.201200015
    Scopus Count
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