4.2 Article

Postfunctionalization of polyoxanorbornene backbone through the combination of bromination and nitroxide radical coupling reactions

Journal

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 53, Issue 20, Pages 2381-2389

Publisher

WILEY
DOI: 10.1002/pola.27697

Keywords

bromination; Controlled; living polymerization (CLP); IR spectroscopy; nitroxide radical coupling (NRC); poly (oxanorbornene imide) (PONB); post-functionalization; ring-opening metathesis polymerization (ROMP) and NMR; UV spectroscopy; 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)

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The brominated backbone of poly(oxanorbornene imide) (PONB) (PONB-Br) was functionalized with 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-acrylate, -epoxy, and poly (ethylene glycol) (PEG) yielding PONB-acrylate, PONB-epoxy, and PONB-PEG through the nitroxide radical coupling (NRC) reaction. Although an excess amount of functional-TEMPOs were used. The observed NRC efficiencies were found in the range of 7-25%. Notably, H-1 NMR spectra of all polymers exhibited a signal at 6.08 ppm after NRC reactions indicating rebuilding of the main chain double bond and further identified by C-13 NMR analysis. The inevitable formation of double bond through the tendency of the recombination of the formed radicals was supported by a separate experiment conducted without utilizing functional-TEMPO. Besides, the versatility of the ROMP backbone further demonstrated by the introduction hetero functionality onto the polymer by a consecutive reactions. (c) 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 2381-2389

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