Functionalized poly(oxanorbornene)‐block‐copolymers: Preparation via ROMP/click‐methodology |
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Authors: | Christian Kluger Wolfgang H. Binder |
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Affiliation: | 1. Division of Macromolecular Chemistry, Institute of Applied Synthetic Chemistry, Vienna University of Technology, Getreidemarkt 9/163/MC, A‐1060 Wien, Austria;2. Division of Macromolecular Chemistry, Institute of Applied Synthetic Chemistry, Vienna University of Technology, Getreidemarkt 9/163/MC, A‐1060 Wien, AustriaDivision of Macromolecular Chemistry, Institute of Applied Synthetic Chemistry, Vienna University of Technology, Getreidemarkt 9/163/MC, A‐1060 Wien, Austria |
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Abstract: | Block copolymers on basis of poly(oxanorbornenes) bearing functional moieties in their side‐chains are prepared via a combination of ROMP‐methods and 1,3‐dipolar‐“click”‐reactions. Starting from N‐substituted‐ω‐bromoalkyl‐oxanorbornenes and alkyl‐/perfluoroalkyl‐oxanorbornenes, block copolymers with molecular weights up to 25,000 g mol?1 were generated. Subsequent nucleophilic exchange‐reactions yielded the block‐copolymers functionalized with ω‐azidoalkyl‐moieties in one block. The 1,3‐azide/alkine‐“click” reactions with a variety of terminal alkynes in the presence of a catalyst system consisting of tetrakis(acetonitrile)hexafluorophosphate copper(I) and tris(1‐benzyl‐5‐methyl‐1H‐ [1,2,3]triazol‐4‐ylmethyl)‐amine furnished the substituted block copolymers in high yields, as proven by NMR‐spectroscopy. The resulting polymers were investigated via temperature‐dependent SAXS‐methods, revealing their microphase separated structure as well as their temperature‐dependent behavior. The presented method offers the generation of a large set of different block‐copolymers from only a small set of starting materials because of the high versatility of the “click” reaction, thus enabling a simple and complete functionalization after the initial polymerization reaction. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 485–499, 2007 |
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Keywords: | block copolymers 1,3‐dipolar cycloaddition reaction click‐reaction ROMP synthesis |
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