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Blue-Emitting Soluble Poly(m-phenylenevinylene) Derivatives
Soluble poly(m-phenylenevinylene) derivatives (4) were synthesized via Wittig−Horner reaction. The number-average degree of polymerization was estimated to be around 25−35. On the basis of FT-IR and 1H NMR spectra, the olefins in the polymers were confirmed to be predominantly in the trans-configura...
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Published in: | Macromolecules 2001-10, Vol.34 (21), p.7300-7305 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Soluble poly(m-phenylenevinylene) derivatives (4) were synthesized via Wittig−Horner reaction. The number-average degree of polymerization was estimated to be around 25−35. On the basis of FT-IR and 1H NMR spectra, the olefins in the polymers were confirmed to be predominantly in the trans-configuration. A model compound, 3,5-distyryl-4-hexyloxytoluene (5), was also synthesized to aid the structural characterization. Comparison of photoabsorption and emission characteristics between 4 and 5 indicated that the m-phenylene effectively interrupted the conjugation, allowing predictable color control in the π-conjugated polymers. At low temperature, the fluorescence of 4 was readily resolved into two peaks, suggesting the predominant emissions were from 0−1 and 0−2 transitions. Polymers 4 were found to be highly luminescent in both solution and film states. LED devices using 4 gave blue EL output (emission λmax at 445 and 462 nm). |
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ISSN: | 0024-9297 1520-5835 |
DOI: | 10.1021/ma0108923 |