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- W2149798336 abstract "A series of blue-emitting triarylamines containing pyrene and hexaphenylbenzene dendrons were successfully synthesized by employing the Diels–Alder and palladium catalyzed C–N coupling reactions. They display high glass transition temperatures (>140 °C) in differential scanning calorimetry and facile reversible oxidation couple in cyclic voltammetry. They are also thermally stable exhibiting decomposition temperature above 385 °C. Efficient blue-emitting electroluminescent devices were fabricated using these novel amines as the hole transporting layer and 1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene (TPBI) as the electron transporting layer. Colour mixing or green emission was observed when tris(8-hydroxyquinoline)aluminium (Alq3) was used as the electron transporting layer. However insertion of a thin layer of TPBI or 1,3,5-tris(4-tert-butylphenyl-1,3,4-oxadiazolyl)benzene (TPOB) in between the HTL and Alq3 layers led to pure blue emission owing to the confinement of recombination inside the HTL layer containing the compounds." @default.
- W2149798336 created "2016-06-24" @default.
- W2149798336 creator A5030027887 @default.
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- W2149798336 date "2005-01-01" @default.
- W2149798336 modified "2023-10-16" @default.
- W2149798336 title "Hexaphenylphenylene dendronised pyrenylamines for efficient organic light-emitting diodes" @default.
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- W2149798336 doi "https://doi.org/10.1039/b509325b" @default.
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