Polymers Derived from 3,6-Fluorene and Tetraphenylsilane Derivatives: Solution-Processable Host Materials for Green Phosphorescent OLEDs
Author(s) -
Huan-Chi Yeh,
ChenHan Chien,
PingI Shih,
MaoChuan Yuan,
ChingFong Shu
Publication year - 2008
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/ma800391e
Subject(s) - fluorene , phosphorescence , polymer , materials science , carbazole , copolymer , monomer , thermal stability , polymer chemistry , glass transition , oled , polyfluorene , iridium , silane , photochemistry , chemical engineering , chemistry , layer (electronics) , organic chemistry , catalysis , nanotechnology , composite material , fluorescence , physics , quantum mechanics , engineering
We have synthesized two fluorene-based polymeric host materials, P1 and P2, through palladium-catalyzed Suzuki couplings of monomers containing tetraphenylsilane and 3,6-disubstituted fluorene frameworks, respectively. The resultant copolymers exhibited high glass transition temperatures (Tg ≥ 215 °C) and excellent thermal stability. The conjugation lengths of polymers P1 and P2 were effectively confined through the presence of the 3,6-linkages and silane units in the polymer skeleton. The structural features endowed these copolymers with UV−violet emissions in the solid state, together with high triplet energies (ET = 2.60 eV), which were sufficiently high for P1 and P2 to serve as appropriate hosts for green-emitting phosphors. In the case of polymer P2, the incorporation of pendent carbazole groups increased the HOMO level markedly and balanced the rates of charge injection and transportation. Employing P2 doped with green-emitting fac-tris(2-phenylpyridine)iridium as the emissive layer, we fabricated ...
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