Diels-Alder reactions as an efficient route to high purity cyclic polymers
Glassner, Mathias , Blinco, James P., & Barner-Kowollik, Christopher (2011) Diels-Alder reactions as an efficient route to high purity cyclic polymers. Macromolecular Rapid Communications, 32(9-10), pp. 724-728.
A simple and efficient route for the synthesis of cyclic polymer systems is presented. Linear furan protected α-maleimide-ω-cyclopentadienyl functionalized precursors (poly(methyl methacrylate) and poly(tert-butyl acrylate)) were synthesized via atom transfer radical polymerization (ATRP) and subsequent substitution of the bromine end-group with cyclopentadiene. Upon heating at high dilution, deprotection of the dieneophile occurs followed by an intramolecular Diels–Alder reaction yielding a high purity cyclic product.
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|Item Type:||Journal Article|
|Keywords:||atom transfer radical polymerization;cyclic polymers;Diels–Alder reactions|
|Subjects:||Australian and New Zealand Standard Research Classification > CHEMICAL SCIENCE (030000) > MACROMOLECULAR AND MATERIALS CHEMISTRY (030300)|
Australian and New Zealand Standard Research Classification > CHEMICAL SCIENCE (030000) > MACROMOLECULAR AND MATERIALS CHEMISTRY (030300) > Synthesis of Materials (030306)
|Divisions:||Past > Schools > Chemistry|
Past > QUT Faculties & Divisions > Faculty of Science and Technology
|Deposited On:||13 Sep 2011 08:29|
|Last Modified:||13 Sep 2011 08:29|
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