Article
Synthesis and characterization of soluble conjugated polymers having pyrene moiety in the main chain
Article first published online: 13 OCT 2010
DOI: 10.1002/pola.24369
Copyright © 2010 Wiley Periodicals, Inc.
Issue

Journal of Polymer Science Part A: Polymer Chemistry
Volume 48, Issue 23, pages 5562–5569, 1 December 2010
Additional Information
How to Cite
Chen, H., Hu, X. and Ng, S.-C. (2010), Synthesis and characterization of soluble conjugated polymers having pyrene moiety in the main chain. J. Polym. Sci. A Polym. Chem., 48: 5562–5569. doi: 10.1002/pola.24369
Publication History
- Issue published online: 28 OCT 2010
- Article first published online: 13 OCT 2010
- Manuscript Accepted: 1 SEP 2010
- Manuscript Received: 7 JUN 2010
Funded by
- PMED. Grant Number: SERC 052 117 0029
- Abstract
- Article
- References
- Cited By
Keywords:
- conjugated polymers;
- polycondensation;
- pyrene;
- thiophene;
- UV–vis spectroscopy
Abstract
Three new alternating conjugated polymers consisting of pyrene and 3-dodecylthiophene (PPyMT), 4,4′-didodecyl-2,2′-bithiophene (PPyBT), or 9,9-didodecylfluorene (PPyFlu) moieties have been prepared using Suzuki coupling reaction or Sugimoto approaches. The polymers were readily soluble in common organic solvents and exhibited good thermal stability in nitrogen and air atmospheres. The structures and optical properties of the polymers were characterized by NMR, FTIR, XRD, UV–vis, and fluorescence spectroscopy. PPyMT and PPYBT showed blue-light emission in solution, whereas PPyFlu performed blue-light emitting in film state. The polymers exhibited an intermolecular aggregation and structural ordering due to pyrene–pyrene π–π stacking interaction. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010

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