Cruciform p–n diblock conjugated oligomers for electroluminescent applications
- 20 March 2006
- journal article
- letter
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 30 (5) , 667-670
- https://doi.org/10.1039/b517067b
Abstract
The optoelectronic properties of the cruciform p–n diblock oligomers 1–3 can be independently tuned by the oligofluorene and oxadiazole branches to increase the charge mobility.Keywords
This publication has 20 references indexed in Scilit:
- Cruciform π-systems: effect of aggregation on emissionChemical Communications, 2004
- Cruciform π-systems: hybrid phenylene-ethynylene/phenylene-vinylene oligomersChemical Communications, 2003
- Highly Efficient Blue-Light-Emitting Diodes from Polyfluorene Containing Bipolar Pendant GroupsMacromolecules, 2003
- Cruciform π-Systems for Molecular Electronics ApplicationsJournal of the American Chemical Society, 2003
- Band Gap Engineering of Poly(p-phenyleneethynylene)s: Cross-Conjugated PPE−PPV HybridsMacromolecules, 2002
- Blue-Light-Emitting Fluorene-Based Polymers with Tunable Electronic PropertiesChemistry of Materials, 2001
- Photoluminescent Poly(p-phenylenevinylene)s with an Aromatic Oxadiazole Moiety as the Side Chain: Synthesis, Electrochemistry, and Spectroscopy StudyMacromolecules, 1999
- Iterative Synthesis and Properties of Cross-Conjugated iso-Polydiacetylene OligomersJournal of the American Chemical Society, 1999
- Tuning Redox Behavior and Emissive Wavelength of Conjugated Polymers by p−n Diblock StructuresJournal of the American Chemical Society, 1998
- Synthesis and Characterization of a New p−n Diblock Light-Emitting CopolymerMacromolecules, 1998