Abstract
Two new blue-light-emitting polyphosphazenes (1 and 2) containing carbazolyl groups as side chains were synthesized from a highly reactive macromolecular intermediate by a nucleophilic substitution reaction. Molecular structural characterization for the polymers was presented by 1H NMR, IR, and ultraviolet-visible spectra, gel permeation chromatography, and differential scanning calorimetry. The polymers exhibited excellent solubility in common organic solvents and were thermally stable. A fluorescence analysis of the two materials in tetrahydrofuran showed a strong blue light emitting. The quantum yields of the polyphosphazenes were 0.55 for 1 and 0.64 for 2, relative to quinoline (in 0.1 N H2SO4). An electroluminescent diode was fabricated, and a bright blue light was observed; the maximum external quantum efficiency was about 0.026% at an applied forward voltage of 23 V.
| Original language | English |
|---|---|
| Pages (from-to) | 3428-3433 |
| Number of pages | 6 |
| Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
| Volume | 39 |
| Issue number | 19 |
| DOIs | |
| State | Published - 1 Oct 2001 |
| Externally published | Yes |
Keywords
- Luminescence
- Polyphosphazenes
- Synthesis
Fingerprint
Dive into the research topics of 'Synthesis and luminescence of polyphosphazenes with carbazolyl side chains'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver