Extended conjugation in poly(triarylamine)s:synthesis, structure and impact on field-effect mobility

Sprick, Reiner Sebastian and Hoyos, Mario and Wrackmeyer, Marion Sofia and Parry, Adam Valentine Sheridan and Grace, Iain Mark and Lambert, Colin and Navarro, Oscar and Turner, Michael Lewis (2014) Extended conjugation in poly(triarylamine)s:synthesis, structure and impact on field-effect mobility. Journal of Materials Chemistry C, 2 (32). pp. 6520-6528. ISSN 2050-7526

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Abstract

Polytriarylamines with extended fused backbones are accessible by the coupling of anilines with dibromoarenes based on substituted indenofluorenes, diindenofluorenes, carbazoles and indolocarbazoles. The optical and electrochemical properties of these polymers show an increase in the HOMO energy levels and the onset of absorption on extending the length of the fused ring segment. The polymer derived from the indenofluorene unit shows the highest reported performance for a polytriarylamine in an OFET and this observation can be rationalized by DFT calculations of model oligomers that show higher calculated reorganization energies for the more extended diindenofluorene units.

Item Type:
Journal Article
Journal or Publication Title:
Journal of Materials Chemistry C
Additional Information:
This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/2500/2505
Subjects:
?? LIGHT-EMITTING-DIODESCHARGE-CARRIER MOBILITYEFFECT TRANSISTORSP-PHENYLENEELECTROLUMINESCENT DEVICESSEMICONDUCTING POLYMERSORGANIC SEMICONDUCTORSTRIARYLAMINE POLYMERSSOLAR-CELLSPOLYTRIPHENYLAMINECHEMISTRY(ALL)MATERIALS CHEMISTRY ??
ID Code:
72157
Deposited By:
Deposited On:
15 Dec 2014 13:39
Refereed?:
Yes
Published?:
Published
Last Modified:
17 Sep 2023 01:35