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A First Synthesis and Physical Properties of Asymmetric Anthracenes-Thiophenes Bridged with Ethylene SCIE SCOPUS KCI

Title
A First Synthesis and Physical Properties of Asymmetric Anthracenes-Thiophenes Bridged with Ethylene
Authors
Hwang, MJPark, JHJeong, EBKang, IDong Hoon LeePark, CESingh, OMChoi, HKim, YHYoon, YJKwon, SKLee, SG
Date Issued
2012-11-20
Publisher
KOREAN CHEMICAL SOCIETY
Abstract
Here we report our recent result of a new semiconductor material, which has an asymmetric structure. The synthesized molecules consist of anthracene and thiophene connected by bridged ethylene and substituted with hexyl or dodecyl groups as pendants. The semiconductors were synthesized using a McMurry coupling reaction between anthracene-2-carbaldehyde and corresponding 5-hexyl(or dodecyl)thiophene-2-carbaldehyde. A first investigation of synthesized asymmetry AVHT (9a) and AVDT (9b) for the physical properties showed that they have high oxidation potential and thermal stability. The devices prepared by using AVHT (9a) and AVDT (9b) showed the mobility of 2.6 x 10(-2) cm(2)/Vs and 4.4 x 10(-3) cm(2)/Vs, respectively, in solution processed OTFTs.
Keywords
Organic thin-film transistors; McMurry coupling; Asymmetric anthracene derivatives; Solution-processing; p-Type charge carrier mobility; THIN-FILM TRANSISTORS; FIELD-EFFECT TRANSISTORS; END-CAPPED OLIGOMERS; HIGH-PERFORMANCE SEMICONDUCTORS; ORGANIC SEMICONDUCTORS; DERIVATIVES; ELECTRONICS; NAPHTHALENE; MOLECULES; MOBILITY
URI
https://oasis.postech.ac.kr/handle/2014.oak/15542
DOI
10.5012/BKCS.2012.33.11.3810
ISSN
0253-2964
Article Type
Article
Citation
Korean Chemical Society. Bulletin, vol. 33, no. 11, page. 38103816 - 3816, 2012-11-20
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박찬언PARK, CHAN EON
Dept. of Chemical Enginrg
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