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H-shaped anthracene-based semiconducting molecules bearing a 9,10-bis((4-hexylphenyl)ethynyl)anthracene dimer

Authors
Kim, Kyung HwanShin, JicheolChoi, Dong Hoon
Issue Date
8월-2012
Publisher
ELSEVIER SCIENCE SA
Keywords
Conjugated molecules; Anthracene; Semiconductor; Mobility; Organic thin film transistor
Citation
SYNTHETIC METALS, v.162, no.13-14, pp.1140 - 1146
Indexed
SCIE
SCOPUS
Journal Title
SYNTHETIC METALS
Volume
162
Number
13-14
Start Page
1140
End Page
1146
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/107820
DOI
10.1016/j.synthmet.2012.05.001
ISSN
0379-6779
Abstract
We have successfully synthesized and characterized H-shaped anthracene-based semiconducting molecules that are solution processable. They were synthesized using 9,10-bis((4-hexylphenyl)ethynyl)anthracene via the Stille coupling reaction. The two molecules not only form uniformly smooth films on large surfaces but also show better homogeneous layer formation with relatively small crystallites. The semiconducting properties of the two pi-conjugated molecules, 3 and 4. were evaluated by using the molecules in organic thin-film transistors (OTFTs). As-spun films of these molecules showed fairly high charge carrier mobilities of around 0.013-0.037 cm(2) V-1 s(-1) (I-on/I-off > 10(4-5)) without additional thermal treatment. The molecule bearing a bithiophene connecting group unexpectedly showed relatively poor carrier mobility, which is attributed to a less-ordered structure and poor anisotropic arrangement of the crystallites without annealing process. (C) 2012 Elsevier B.V. All rights reserved.
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CHOI, DONG HOON
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