journal article·2011-09-13

Benzotrithiophene Co-polymers with High Charge Carrier Mobilities in Field-Effect Transistors

Bob C. Schroeder, Christian B. Nielsen, Young Ju Kim, Jeremy Smith, Zhenggang Huang, James Durrant, Scott E. Watkins, Kigook Song, Thomas D. Anthopoulos, Iain McCulloch

Chemistry of Materials· Volume 23· Issue 17
Publisher page

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 cm 2 /(V s).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Molecular Junctions and Nanostructures · Thin-Film Transistor Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and Centre for Plastic Electronics, Imperial College London, London SW7 2AZ, United Kingdom

Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea

Department of Physics and Centre for Plastic Electronics, Imperial College London, London SW7 2AZ, United Kingdom

CSIRO Materials Science and Engineering, VIC 3169, Victoria, Australia

References (19)

Show source-provided references
1. Katz H. E. · Chem. Mater. · 2004 · 16 · 474810.1021/cm049781j ↗
2. Zaumseil J. · Chem. Rev. · 2007 · 107 · 129610.1021/cr0501543 ↗
3. McCulloch I. · Adv. Mater. · 2009 · 21 · 109110.1002/adma.200801650 ↗
4. Facchetti A. · Chem. Mater. · 2011 · 23 · 73310.1021/cm102419z ↗
5. Sun J. · Adv. Funct. Mater. · 2011 · 21 · 2910.1002/adfm.201001530 ↗
6. Garnier F. · Science · 1994 · 265 · 186410.1126/science.265.5179.1684 ↗
7. McCulloch I. · Nat. Mater. · 2006 · 5 · 32810.1038/nmat1612 ↗
8. Osaka I. · J. Am. Chem. Soc. · 2010 · 132 · 500010.1021/ja101125p ↗
9. Li Y. · Adv. Mater. · 2010 · 22 · 486210.1002/adma.201002313 ↗
10. Zhang W. · J. Am. Chem. Soc. · 2010 · 132 · 1143710.1021/ja1049324 ↗
11. Bronstein H. · J. Am. Chem. Soc. · 2011 · 133 · 327210.1021/ja110619k ↗
12. Lei T. · J. Am. Chem. Soc. · 2011 · 133 · 609910.1021/ja111066r ↗
13. Nielsen C. B. · Org. Lett. · 2011 · 13 · 241410.1021/ol200643z ↗
14. Rieger R. · Chem. Mater. · 2010 · 22 · 531410.1021/cm101577j ↗
15. Osaka I. · J. Am. Chem. Soc. · 2011 · 133 · 685210.1021/ja201591a ↗
16. Scheibe G. · Angew. Chem. · 1937 · 50 · 21210.1002/ange.19370501103 ↗
17. Menzel H. · Langmuir · 1994 · 10 · 192610.1021/la00018a052 ↗
18. Kim S.-o. · Adv. Funct. Mater. · 2011 · 21 · 161610.1002/adfm.201002367 ↗
19. Kline R. J. · Macromolecules · 2005 · 38 · 331210.1021/ma047415f ↗