The Synthesis And Optoelectronic Properties Of Oxadiazole-Based Polymers
- 1 January 1995
- journal article
- Published by Springer Nature in MRS Proceedings
Abstract
New oxadiazole-based polymeric materials have been synthesized either as side chain copolymers with polymethacrylate or as main chain copolymers carrying solubilizing elements such as hexafluoropropylidene or meta-linked aromatic spacer units. Many of these materials exhibit blue luminescence in the solid state. The materials have been evaluated by photoluminescence and cyclic voltammetry studies, and as the electron transporting layer in a two-layer electroluminescent device with poly(p-phenylenevinylene) (PPV) as the emissive layer. The major conclusion is that these materials function by providing large heterojunction offsets at the Highest Occupied Molecular Orbital (HOMO) which block the passage of holes through the device.Keywords
This publication has 18 references indexed in Scilit:
- 1,3,4-Oxadiazole-Containing Polymers as Electron-Injection and Blue Electroluminescent Materials in Polymer Light-Emitting DiodesChemistry of Materials, 1995
- Bright blue electroluminescence from an oxadiazole‐containing copolymerAdvanced Materials, 1995
- Electron injection polymer for polymer light-emitting diodesJournal of Applied Physics, 1995
- Design and Application of Electron-Transporting Organic MaterialsScience, 1995
- Electrical Properties of Pyrolyzed and Electrochemically Lithium-Doped Poly(hydrazocarbonyl-1,4-phenylenecarbonyl) FilmJapanese Journal of Applied Physics, 1994
- Efficient light-emitting diodes based on polymers with high electron affinitiesNature, 1993
- Light-emitting diodes based on conjugated polymersNature, 1990
- High‐strength, high‐modulus fibers from hydrazide polymers and copolymersJournal of Applied Polymer Science, 1979
- 2,5-Diaryloxazoles and 2,5-Diaryl-1,3,4-oxadiazolesJournal of the American Chemical Society, 1955
- Chemotherapy of Experimental Tuberculosis. VIII. The Synthesis of Acid Hydrazides, their Derivatives and Related Compounds1,2Journal of the American Chemical Society, 1953