Abstract
The degrdn. of two defect-free pi-conjugated oligomers and the participation of their solubilizing side chains in the process are studied in unprecedented detail. The detected intermediate products reveal a mechanism of successive shortening of alkyl and oligo(ethylene glycol) substituents. Eventually, these processes cause chem. modifications in the conjugated backbone, which strongly influence the electronic properties of the materials.
Original language | English |
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Pages (from-to) | 597-602 |
Journal | Advanced Materials |
Volume | 21 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2009 |