Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors

碩士 === 國立中央大學 === 化學學系 === 106 === New small molecules based on TSBT, DSDTT, and SeBT cores have been synthesized for organic thin film transistors (OTFTs). For the first TSBT series, n-type TSBTQ-14 (TSBTQ with C14H29 chains) and TSBTQ-6 (TSBTQ with C6H13 chains) exhibited mobility of 0.14 cm2V-1s-...

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Main Authors: Chang-Hui Cho, 卓長輝
Other Authors: Ming-Chou Chen
Format: Others
Language:en_US
Published: 2018
Online Access:http://ndltd.ncl.edu.tw/handle/gbp646
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spelling ndltd-TW-106NCU050650542019-11-14T05:35:43Z http://ndltd.ncl.edu.tw/handle/gbp646 Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors 具硫醚及硒醚鏈之可溶性有機薄膜電晶體噻吩小分子之開發 Chang-Hui Cho 卓長輝 碩士 國立中央大學 化學學系 106 New small molecules based on TSBT, DSDTT, and SeBT cores have been synthesized for organic thin film transistors (OTFTs). For the first TSBT series, n-type TSBTQ-14 (TSBTQ with C14H29 chains) and TSBTQ-6 (TSBTQ with C6H13 chains) exhibited mobility of 0.14 cm2V-1s-1 and 0.10 cm2V-1s-1. To further complete the side chains effect study, TSBTQ-10 (1; TSBTQ with C10H21 chains) was synthesized and characterized. Via solution shearing, TSBT-10 exhibits the best mobility up to 0.18 cm2V-1s-1 in this series. For the second DSDTT series, DDTT-DSDTT-10 (DSDTT with C10H21 chains) exhibited high mobility 2.6 cm2V-1s-1. To further complete the side chains effect study, DDTT-DSDTT-8 (2; with C8H17 chains) was synthesized and characterized. Via solution shearing, DDTT-DSDTT-8 demonstrates the best mobility up to 3.2 cm2V-1s-1. Both molecular structures of DSDTTs were determined by single crystal X-ray diffraction and exhibits two parallel face-to-face columnar stacking’s with a very close interplanar core distance of 3.6 Å . For the third series, a couple new small molecules based on the selenylated bithiophene (SeBT) with different end-capped aromatic groups and alkyl chains were developed. DDTT-SeBT-14 (7; with C14H29 chains) exhibits the highest mobility of 4.00 cm2V-1s-1 via solution shearing. The molecular structures of DDTT-SeBT-14 and DDTT-SeBT-10 (6) were determined by single crystal X-ray diffraction and showed brick-type iv molecular stacking. Ming-Chou Chen 陳銘洲 2018 學位論文 ; thesis 190 en_US
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language en_US
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description 碩士 === 國立中央大學 === 化學學系 === 106 === New small molecules based on TSBT, DSDTT, and SeBT cores have been synthesized for organic thin film transistors (OTFTs). For the first TSBT series, n-type TSBTQ-14 (TSBTQ with C14H29 chains) and TSBTQ-6 (TSBTQ with C6H13 chains) exhibited mobility of 0.14 cm2V-1s-1 and 0.10 cm2V-1s-1. To further complete the side chains effect study, TSBTQ-10 (1; TSBTQ with C10H21 chains) was synthesized and characterized. Via solution shearing, TSBT-10 exhibits the best mobility up to 0.18 cm2V-1s-1 in this series. For the second DSDTT series, DDTT-DSDTT-10 (DSDTT with C10H21 chains) exhibited high mobility 2.6 cm2V-1s-1. To further complete the side chains effect study, DDTT-DSDTT-8 (2; with C8H17 chains) was synthesized and characterized. Via solution shearing, DDTT-DSDTT-8 demonstrates the best mobility up to 3.2 cm2V-1s-1. Both molecular structures of DSDTTs were determined by single crystal X-ray diffraction and exhibits two parallel face-to-face columnar stacking’s with a very close interplanar core distance of 3.6 Å . For the third series, a couple new small molecules based on the selenylated bithiophene (SeBT) with different end-capped aromatic groups and alkyl chains were developed. DDTT-SeBT-14 (7; with C14H29 chains) exhibits the highest mobility of 4.00 cm2V-1s-1 via solution shearing. The molecular structures of DDTT-SeBT-14 and DDTT-SeBT-10 (6) were determined by single crystal X-ray diffraction and showed brick-type iv molecular stacking.
author2 Ming-Chou Chen
author_facet Ming-Chou Chen
Chang-Hui Cho
卓長輝
author Chang-Hui Cho
卓長輝
spellingShingle Chang-Hui Cho
卓長輝
Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors
author_sort Chang-Hui Cho
title Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors
title_short Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors
title_full Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors
title_fullStr Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors
title_full_unstemmed Development of Solution Processable Thioalkylated and Selenalkylated Thiophenes for Small Molecular Organic Thin Film Transistors
title_sort development of solution processable thioalkylated and selenalkylated thiophenes for small molecular organic thin film transistors
publishDate 2018
url http://ndltd.ncl.edu.tw/handle/gbp646
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