Abstract
A novel synthesis is presented of a fourfold ethynyl-substituted perylene diimide dye 4, which acts as a core molecule for the buildup of polyphenylene dendrimers. Around the luminescent core 4, a first-generation (5), a second-generation (6), and a third-generation (7) polyphenylene dendritic environment consisting of pentaphenylbenzene building blocks are constructed. The dendrimers 5 and 6 are synthesized by an exclusively divergent route, whereas for 7, a combination of a divergent and convergent approaches is applied. Absorption and emission spectra of 5 - 7 in different solvents and in a film have been measured and compared to a nondendronized model compound 13. In solution, the internal chromophore is scarcely influenced by the dendritic scaffold; however, in the solid state, aggregation of the perylene diimide is prevented very effectively by the four rigid dendrons. Additionally, fluorescence quantum yields in solution have been determined for 5 - 7 and 13; they decrease as the number of generation increases.
| Original language | English |
|---|---|
| Pages (from-to) | 4844-4853 |
| Number of pages | 10 |
| Journal | Chemistry |
| Volume | 7 |
| Issue number | 22 |
| Publication status | Published - 2001 |
Keywords
- perylenes
- dyes/pigments
- dendrimers
- cycloaddition
- aggregation