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). © 2011 American Chemical Society.
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Schroeder, B. C., Nielsen, C. B., Kim, Y. J., Smith, J., Huang, Z., Durrant, J., … McCulloch, I. (2011). Benzotrithiophene Co-polymers with high charge carrier mobilities in field-effect transistors. Chemistry of Materials, 23(17), 4025–4031. https://doi.org/10.1021/cm2015884
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