Abstract
In this paper we present the synthesis and characterization of a new light-emitting copolymer constituted of regularly alternating segments of 3,3′-didecyl-2,2′-bithiophene and 2,6-bis(1,3,4-oxadiazolyl)-toluene, which are p-dopable and n-dopable, respectively. The new polymer emits intense green light under the irradiation of UV light in its film states and shows strong solvatochromism both on absorption and on emission. The n-doping potential of the polymer is measured to be similar with that of 2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD) and other reported oxadiazole-containing polymers, the currently excellent electron-transporting materials, while its p-doping potential is much lower than those of other oxadiazole-containing light-emitting polymers and is comparable with that of poly-(p-phenylenevinylene) (PPV) and polythiophenes (PT), the typical p-dope type materials. The presented synthesis reveals a possible approach to balance the rates of injection of electrons and holes from opposite contacts into an emissive layer in polymer light-emitting diodes by controlling the intrinsic properties of light-emitting materials.
Original language | English |
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Pages (from-to) | 4838-4844 |
Number of pages | 7 |
Journal | Macromolecules |
Volume | 31 |
Issue number | 15 |
DOIs | |
State | Published - 28 Jul 1998 |
Externally published | Yes |