Suzuki Coupling Reaction of 1,6,7,12-Tetrabromoperylene Bisimide
Organic Letters2006Vol. 8(5), pp. 867–870
Citations Over TimeTop 10% of 2006 papers
Abstract
1,6,7,12-Tetrabromoperylene-3,4,9,10-tetracarboxylic acid bisanhydride and the corresponding tetrabrominated perylene bisimide were first synthesized with high yields. The Suzuki coupling reaction of novel tetrabromoperylene bisimide with phenylbonoric acid was studied. The four bromines in the bay position of the perylene core were substituted successfully to yield 1,6,7,12-teraphenylperylene bisimide. The photochemical properties of the novel perylene bisimides were studied and presented.
Related Papers
- → Perylene monoanhydride diester: a versatile intermediate for the synthesis of unsymmetrically substituted perylene tetracarboxylic derivatives(2008)47 cited
- → Theoretical investigations on absorption and fluorescence of perylene and its tetracarboxylic derivatives(1997)30 cited
- → Annellation effects in the perylene and coronene series(1966)13 cited
- → Perylene Pigments(2009)13 cited
- → Simultaneous determination of perylene and benzo[g,h,i]perylene by synchronous fluorescence using a micellar system(1992)10 cited