Abstract
The successful design and synthesis of two novel benzo[1,2-b:3,4-b′: 5,6-d′]trithiophene-containing polymers is presented. The planar benzotrithiophene core induces strong aggregation effects in alternating co-polymers with both thiophene and thieno[3,2-b]thiophene. Co-monomer choice is found to play a crucial role in determining the backbone conformation, the interchain interactions, and the polymer solubility. Despite molecular disorder introduced by a branched solubilizing alkyl chain and a regiorandom polymerization of the asymmetric benzotrithiophene unit, these co-polymers exhibit hole mobilities as high as 0.24 cm2/(V s).
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4025-4031 |
| Number of pages | 7 |
| Journal | Chemistry of Materials |
| Volume | 23 |
| Issue number | 17 |
| DOIs | |
| State | Published - Sep 13 2011 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General Chemistry
- General Chemical Engineering
- Materials Chemistry
Keywords
- Transistors
- benzotrithiophene
- conjugated polymers
- holemobility