| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218928 | Tetrahedron | 2013 | 6 Pages |
Abstract
Dissymmetric Ï-conjugated oligomers incorporating 3,4-ethylenedioxythiophene (EDOT) units and bearing nitro and amino end-groups were synthesized in good yields through Pd-catalyzed Suzuki coupling reactions and direct C-H bond arylation. Their spectroscopic properties show that they have a low HOMO-LUMO gap. They are easily oxidized at low potential and could be used in various applications ranging from photovoltaics to molecular electronics.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Gaëlle Trippé-Allard, Jean-Christophe Lacroix,