Abstract
Typical syntheses of conjugated polymers rely heavily on organometallic reagents and metal-catalyzed cross-coupling reactions. Here, we show that an environmentally benign aldol polymerization can be used to synthesize poly(bisisoindigo), an analog of polyisoindigo with a ring-fused structural repeat unit. Owing to its extended conjugation length, poly(bisisoindigo) absorbs across the UV/vis/NIR spectrum, with an absorption tail that reaches 1000 nm. Due to the four electron-deficient lactam units on each repeat unit, poly(bisoindigo) possesses a low-lying LUMO, which lies at -3.94 eV relative to vacuum. Incorporation of the ring-fused monomer unit also lowered the overall torsional strain in the polymer backbone (relative to polyisoindigo), and the polymer was successfully used in prototype unipolar n-channel organic thin-film transistors.
| Original language | English |
|---|---|
| Pages (from-to) | 14265-14271 |
| Number of pages | 7 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 12 |
| Issue number | 12 |
| DOIs | |
| State | Published - 25 Mar 2020 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 American Chemical Society.
Keywords
- OTFTs
- aldol polymerization
- charge transport
- conjugated polymers
- organic thin-film transistors
ASJC Scopus subject areas
- General Materials Science