TY  - JOUR
A1  - Qu, J. Q.
A1  - Zhang, J. Y.
A1  - Grimsdale, A. C.
A1  - Mullen, K.
A1  - Jaiser, Frank
A1  - Yang, X. H.
A1  - Neher, Dieter
T1  - Dendronized perylene diimide emitters : Synthesis, luminescence, and electron and energy transfer studies
N2  - Aggregation of chromophores in the solid state commonly causes undesirable red shifts in the emission spectra and/or emission quenching. To overcome this problem, we have prepared soluble perylenetetracarboxidiimide dyes in which the chromophores are effectively shielded by polyphenylene dendrimers attached in the bay positions. Models show that attachment of the shielding units in the bay position should provide more efficient shielding than attaching them via the imide moieties. The dendrimers possess excellent film-forming properties due to alkyl substituents on their peripheries. The lack of a red shift in emission upon going from solution to the solid state indicates the dendrons suppress interaction of the emissive cores, leading to pure red-orange emission. Single-layer LEDs produce red-orange emission with relatively low efficiency especially for the higher generation dendrons, which is attributed to poor charge conduction. LEDs using blends of the dendrimers and the undendronized dye as a model compound in PVK have been investigated, and a model to extract relative charge injection rates through the dendritic scaffold from the spectral contributions in the EL spectra is developed
Y1  - 2004
SN  - 0024-9297
ER  -