Abstract
We report an electrochemical transformation of binaphthols to give peri-xanthenoxanthene (PXX) groups in small molecules and within polymer backbones. The monomer 7,7-bis(2,2-bithiophen-5-yl)-1,1-bi-2,2-naphthol (2) was subjected to electropolymerization, resulting in the segmented conducting polymer that is stable at low potentials. However, high-potential electrochemical oxidation promoted cyclization of binaphthol units gives PXX, which transforms the moderately conducting segmented polymer into a highly conducting fully conjugated polymer. This oxidative cyclization is a highly effective means by which to incorporate a planar polycyclic heteroaromatic structure (i.e., PXX) into thiophene-based conducting polymers. A model compound study conclusively proved the proposed oxidative cyclization scheme.
| Original language | English |
|---|---|
| Pages (from-to) | 1472-1475 |
| Number of pages | 4 |
| Journal | Macromolecules |
| Volume | 42 |
| Issue number | 5 |
| DOIs | |
| State | Published - 10 Mar 2009 |
| Externally published | Yes |