Issue 2, 2012

Alkyne–azide coupling of tailored poly(vinylidene fluoride) and polystyrene for the synthesis of block copolymers

Abstract

The synthesis of block copolymers consisting of poly(vinylidene fluoride) (PVDF) and polystyrene (PS) is reported. Firstly, a propargyl-functionalized alkoxyamine initiator (PgOTIPNO) was prepared and subsequently used for the preparation of a propargyl-terminated PS homopolymer of different chain lengths with low dispersities via nitroxide-mediated radical polymerization. A tailored PVDF homopolymer with iodine end groups originating from iodine transfer polymerization was transformed to PVDF with azide end group. Then, alkyne-terminated PS with different molecular weights and azide-terminated PVDF were joined together via copper-catalyzed alkyneazide coupling. The block copolymers were characterized using 1H-NMR, 19F-NMR, IR, SEC, and DSC.

Graphical abstract: Alkyne–azide coupling of tailored poly(vinylidene fluoride) and polystyrene for the synthesis of block copolymers

Supplementary files

Article information

Article type
Paper
Submitted
21 Sep 2011
Accepted
10 Nov 2011
First published
01 Dec 2011

Polym. Chem., 2012,3, 409-414

Alkyneazide coupling of tailored poly(vinylidene fluoride) and polystyrene for the synthesis of block copolymers

R. Vukićević, U. Schwadtke, S. Schmücker, P. Schäfer, D. Kuckling and S. Beuermann, Polym. Chem., 2012, 3, 409 DOI: 10.1039/C1PY00427A

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