Article
Terpyridine-modified poly(vinyl chloride): Possibilities for supramolecular grafting and crosslinking
Article first published online: 8 AUG 2003
DOI: 10.1002/pola.10881
Copyright © 2003 Wiley Periodicals, Inc.
Issue
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Journal of Polymer Science Part A: Polymer Chemistry
Volume 41, Issue 19, pages 2964–2973, 1 October 2003
Additional Information
How to Cite
Meier, M. A. R. and Schubert, U. S. (2003), Terpyridine-modified poly(vinyl chloride): Possibilities for supramolecular grafting and crosslinking. Journal of Polymer Science Part A: Polymer Chemistry, 41: 2964–2973. doi: 10.1002/pola.10881
Publication History
- Issue published online: 8 AUG 2003
- Article first published online: 8 AUG 2003
- Manuscript Accepted: 30 JUN 2003
- Manuscript Received: 13 MAY 2003
Funded by
- Dutch Polymer Institute
- Fonds der Chemischen Industrie
- Abstract
- Article
- References
- Cited By
Keywords:
- poly(vinyl chloride) (PVC);
- terpyridine;
- metal-polymer complexes;
- crosslinking;
- grafting
Graphical Abstract

A schematic representation of functionalized poly(vinyl chloride) (PVC) as it was used for this study. The functionalized material contained metal-ion binding sites, which could be used for crosslinking reactions with transition-metal ions. The complexation of the modified PVC with several transition-metal ions was studied with ultraviolet–visible spectroscopy and gel permeation chromatography.
Abstract
Commercially available poly(vinyl chloride) (PVC) was covalently modified with terpyridine supramolecular binding units in a two-step reaction. First, PVC was modified with aromatic thiols to introduce OH functionalities into the polymer backbone, which were subsequently reacted with an isocyanate-functionalized terpyridine binding unit. The resulting functionalized material contained metal-ion binding sites, which could be used for grafting and crosslinking reactions. A grafting experiment was performed with a small organic terpyridine ligand. The complexation of the modified PVC with several transition-metal ions was studied with ultraviolet–visible spectroscopy and gel permeation chromatography. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2964–2973, 2003

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