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Effects of alkyl chain positioning on conjugated polymer microstructure and field-effect mobilities
Author(s) -
Bob C. Schroeder,
Christian B. Nielsen,
Paul Westacott,
Jeremy Smith,
Stephan Rossbauer,
Thomas D. Anthopoulos,
Natalie Stingelin,
Iain McCulloch
Publication year - 2015
Publication title -
mrs communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.751
H-Index - 31
eISSN - 2159-6859
pISSN - 2159-6867
DOI - 10.1557/mrc.2015.49
Subject(s) - alkyl , materials science , crystallinity , conjugated system , side chain , polymer , solubility , microstructure , chemical engineering , solid state , charge carrier , organic semiconductor , chemical physics , organic chemistry , polymer chemistry , composite material , optoelectronics , chemistry , engineering
Solubilizing alkyl chains play a crucial role in the design of semiconducting polymers because they define the materials solubility and processability as well as both the crystallinity and solid-state microstructure. In this paper, we present a scarcely explored design approach by attaching the alkyl side chains on one side (cis-) or on both sides (trans-) of the conjugated backbone. We further investigate the effects of this structural modification on the solid-state properties of the polymers and on the charge-carrier mobilities in organic thin-film transistors.

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