Synthesis of Soluble Organic Thin film transistors.

碩士 === 國立中央大學 === 化學研究所 === 99 === Asymmetric fused thiophene compound (11) was synthesized by “one-pot” reaction. Based on compound (11), derivatives (1) and (2) have been developed. Both compounds exhibit p-type field-effect performances with mobility of 0.026 and 9x10-4 cm2/Vs via vacuum evaporat...

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Main Authors:	Chia-Ming Yeh, 葉佳明
Other Authors:	Ming-Chou Chen
Format:	Others
Language:	zh-TW
Published:	2011
Online Access:	http://ndltd.ncl.edu.tw/handle/40109234357727157180

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spelling	ndltd-TW-099NCU050650822017-07-07T04:31:05Z http://ndltd.ncl.edu.tw/handle/40109234357727157180 Synthesis of Soluble Organic Thin film transistors. 有機薄膜電晶體材料苯三併環噻吩及可溶性聯噻吩衍生物之開發 Chia-Ming Yeh 葉佳明碩士國立中央大學化學研究所 99 Asymmetric fused thiophene compound (11) was synthesized by “one-pot” reaction. Based on compound (11), derivatives (1) and (2) have been developed. Both compounds exhibit p-type field-effect performances with mobility of 0.026 and 9x10-4 cm2/Vs via vacuum evaporation, respectively. Compounds (3) ~ (9) have been successfully developed based on bithiophene compound (18). Preparation of soluble compound (18) has been improved with better yield. Compounds (6), (7), and (8) exhibit good field-effect performances with high mobility of 0.15, 0.38, and 0.24 cm2/Vs via solution process, respectively. All of these new semiconductor materials exhibit good stability under light, air, and thermal conditions. Ming-Chou Chen 陳銘洲 2011 學位論文 ; thesis 163 zh-TW
collection	NDLTD
language	zh-TW
format	Others
sources	NDLTD
description	碩士 === 國立中央大學 === 化學研究所 === 99 === Asymmetric fused thiophene compound (11) was synthesized by “one-pot” reaction. Based on compound (11), derivatives (1) and (2) have been developed. Both compounds exhibit p-type field-effect performances with mobility of 0.026 and 9x10-4 cm2/Vs via vacuum evaporation, respectively. Compounds (3) ~ (9) have been successfully developed based on bithiophene compound (18). Preparation of soluble compound (18) has been improved with better yield. Compounds (6), (7), and (8) exhibit good field-effect performances with high mobility of 0.15, 0.38, and 0.24 cm2/Vs via solution process, respectively. All of these new semiconductor materials exhibit good stability under light, air, and thermal conditions.
author2	Ming-Chou Chen
author_facet	Ming-Chou Chen Chia-Ming Yeh 葉佳明
author	Chia-Ming Yeh 葉佳明
spellingShingle	Chia-Ming Yeh 葉佳明 Synthesis of Soluble Organic Thin film transistors.
author_sort	Chia-Ming Yeh
title	Synthesis of Soluble Organic Thin film transistors.
title_short	Synthesis of Soluble Organic Thin film transistors.
title_full	Synthesis of Soluble Organic Thin film transistors.
title_fullStr	Synthesis of Soluble Organic Thin film transistors.
title_full_unstemmed	Synthesis of Soluble Organic Thin film transistors.
title_sort	synthesis of soluble organic thin film transistors.
publishDate	2011
url	http://ndltd.ncl.edu.tw/handle/40109234357727157180
work_keys_str_mv	AT chiamingyeh synthesisofsolubleorganicthinfilmtransistors AT yèjiāmíng synthesisofsolubleorganicthinfilmtransistors AT chiamingyeh yǒujībáomódiànjīngtǐcáiliàoběnsānbìnghuánsāifēnjíkěróngxìngliánsāifēnyǎnshēngwùzhīkāifā AT yèjiāmíng yǒujībáomódiànjīngtǐcáiliàoběnsānbìnghuánsāifēnjíkěróngxìngliánsāifēnyǎnshēngwùzhīkāifā
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Synthesis of Soluble Organic Thin film transistors.

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