Abstract
We present the novel 1,4-difunctionalisation of benzocarborane with organometallic groups suitable for cross-coupling and its subsequent insertion for the first time into conjugated polymer backbones. Copolymers with solubilised cyclopentadithiophene and diketopyrrolopyrrole derivatives were prepared by Stille polymerisation in good molecular weight. The physical, material and optoelectronic properties of the resulting polymers were investigated, demonstrating that benzocarborane acts similarly to a stabilised, electron-deficient cis-diene linker. We also report the first polymer field effect transistors incorporating a benzocarborane in the backbone. © The Royal Society of Chemistry.
Original language | English (US) |
---|---|
Pages (from-to) | 232-239 |
Number of pages | 8 |
Journal | Journal of Materials Chemistry C |
Volume | 2 |
Issue number | 2 |
DOIs | |
State | Published - Jan 14 2014 |
Externally published | Yes |