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) |
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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
- benzotrithiophene
- conjugated polymers
- holemobility
- Transistors