Abstract
In this Letter, we report a facile approach to synthesize unsymmetrical 1-bromo-7-alkoxyl perylene diimides by the nucleophilic substitution of one of the two 1,7-dibromo units with an alkyl alcohol using K 2CO 3 as the base. A further replacement of another bromo, for example, by using 4-hydroxylpyridine resulted in unsymmetrical functionalizations at the 1,7-positions. The optical properties of the unsymmetrical PDI derivative were reported and compared with those of the symmetrical derivative.
Original language | English |
---|---|
Pages (from-to) | 1094-1097 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 53 |
Issue number | 9 |
DOIs | |
Publication status | Published - 29 Feb 2012 |
Keywords
- Nucleophile
- Nucleophilic substitution
- Perylene diimide
- Unsymmetrical functionalization