Abstract
We have prepared poly(3-octyl-2,2′-bithiophene) and poly(3′-octyl-2,2′;5′2″-terthiophene) and found that they show better stability against thermal dedoping than poly(3-octylthiophene). A reduction of the number of alkyl side chains in a regular way lead to better space for the counter ion on doping, more planar π-system and a more rigid polymer backbone, compared to poly(3-octylthiophene).
Original language | English |
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Pages (from-to) | 1227-1231 |
Number of pages | 5 |
Journal | Synthetic Metals |
Volume | 55 |
Issue number | 2 -3 pt 2 |
DOIs | |
Publication status | Published - Jan 1993 |
Event | Proceedings of the International Conference on Science and Technology of Metals - ICSM'92 - Goteborg, Swed Duration: 12 Aug 1992 → 18 Aug 1992 |