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Synthesis and Characterization of π-Conjugated Polymers Based on 2-arylbenzimidazole and 4,7-di-thiophene-2-yl-4,5,6,7-tetrahydro-benzo[1,2,5]thiadiazole
A newly designed 2-arylbenzimidazole derivative which plays a role of co-acceptor unit has been prepared for the synthesis of conjugated polymer. 2-arylbenzimidazole derivative has been incorporated into 4,7-dithiophen-2-yl-benzo(2,1,3)thiadiazole (TBT) and fluorene based alternating copolymers with...
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Published in: | Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003) Pa. : 2003), 2013-01, Vol.581 (1), p.31-37 |
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container_title | Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003) |
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creator | Do, Thu Trang Bae, Jun Huei Yoo, Seong Il Lim, Kwon Taek Woo, Han Young Kim, Joo Hyun |
description | A newly designed 2-arylbenzimidazole derivative which plays a role of co-acceptor unit has been prepared for the synthesis of conjugated polymer. 2-arylbenzimidazole derivative has been incorporated into 4,7-dithiophen-2-yl-benzo(2,1,3)thiadiazole (TBT) and fluorene based alternating copolymers with different ratios of 5 mol.% and 10 mol.% named POFTBT-IMD5, POFTBT-IMD10, respectively. We also synthesized alternating copolymer of 9,9-dioctylfluorene and TBT (POFTBT) to compare physical properties. POFTBT-IMD5, POFTBT-IMD10 films showed absorption peaks at 559 and 555 nm, respectively. The HOMO and LUMO energy levels of POFTBT-IMD5, POFTBT-IMD10 were −5.4/−3.84 eV and −5.4/−3.81 eV, respectively, which were similar to those of POFTBT (−5.3/−3.7 eV). |
doi_str_mv | 10.1080/15421406.2013.808145 |
format | article |
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We also synthesized alternating copolymer of 9,9-dioctylfluorene and TBT (POFTBT) to compare physical properties. POFTBT-IMD5, POFTBT-IMD10 films showed absorption peaks at 559 and 555 nm, respectively. 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We also synthesized alternating copolymer of 9,9-dioctylfluorene and TBT (POFTBT) to compare physical properties. POFTBT-IMD5, POFTBT-IMD10 films showed absorption peaks at 559 and 555 nm, respectively. The HOMO and LUMO energy levels of POFTBT-IMD5, POFTBT-IMD10 were −5.4/−3.84 eV and −5.4/−3.81 eV, respectively, which were similar to those of POFTBT (−5.3/−3.7 eV).</description><subject>2-arylbenzimidazole; benzothiadiazole</subject><subject>conjugated polymer</subject><subject>Copolymers</subject><subject>Crystals</subject><subject>Derivatives</subject><subject>Energy levels</subject><subject>Liquid crystals</subject><subject>low band gap</subject><subject>Physical properties</subject><subject>Polymers</subject><subject>Synthesis</subject><issn>1542-1406</issn><issn>1563-5287</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhSMEEqXwBiyyZBFP_Z_MCsGo0EqVigSsELJuYoe4cuzB9ghlVjwHL8Ur1enAtqt7j-53jnR1quo1wRuCO3xBBKeEY7mhmLBNhzvCxZPqjAjJkKBd-3TdOUUr87x6kdIdxpS3pDur_nxefJ5MsqkGr-vdBBGGbKI9QrbB12Gs__5Gu-DvDj8gG11_Cm6ZTUz1e0hFFoQiiIvrjT_a2Wo4BmcesnjTIm1RnmzYT8YbRNHiEG9EI8slmxxhWnQMaLWGb6ShjfheaND2IeRl9WwEl8yrf_O8-vrh8svuCt3cfrzevbtBA-M4I-BMSyHHVva0Mz0U3UrWc0a3dJRbKeUwEIwFENFTzrdaCACgvGtbw3pg7Lx6c8rdx_DzYFJWs02DcQ68CYekiMCSdaJYC8pP6BBDStGMah_tXN5XBKu1CvW_CrVWoU5VFNvbk836McQZfoXotMqwuBDHCH6wSbFHE-4B4XSQIA</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Do, Thu Trang</creator><creator>Bae, Jun Huei</creator><creator>Yoo, Seong Il</creator><creator>Lim, Kwon Taek</creator><creator>Woo, Han Young</creator><creator>Kim, Joo Hyun</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130101</creationdate><title>Synthesis and Characterization of π-Conjugated Polymers Based on 2-arylbenzimidazole and 4,7-di-thiophene-2-yl-4,5,6,7-tetrahydro-benzo[1,2,5]thiadiazole</title><author>Do, Thu Trang ; Bae, Jun Huei ; Yoo, Seong Il ; Lim, Kwon Taek ; Woo, Han Young ; Kim, Joo Hyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-a43d656f76b28ebaa43763b43292f69666cc1005a15b2449d55aaa24877e3ba33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>2-arylbenzimidazole; benzothiadiazole</topic><topic>conjugated polymer</topic><topic>Copolymers</topic><topic>Crystals</topic><topic>Derivatives</topic><topic>Energy levels</topic><topic>Liquid crystals</topic><topic>low band gap</topic><topic>Physical properties</topic><topic>Polymers</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Do, Thu Trang</creatorcontrib><creatorcontrib>Bae, Jun Huei</creatorcontrib><creatorcontrib>Yoo, Seong Il</creatorcontrib><creatorcontrib>Lim, Kwon Taek</creatorcontrib><creatorcontrib>Woo, Han Young</creatorcontrib><creatorcontrib>Kim, Joo Hyun</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Do, Thu Trang</au><au>Bae, Jun Huei</au><au>Yoo, Seong Il</au><au>Lim, Kwon Taek</au><au>Woo, Han Young</au><au>Kim, Joo Hyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of π-Conjugated Polymers Based on 2-arylbenzimidazole and 4,7-di-thiophene-2-yl-4,5,6,7-tetrahydro-benzo[1,2,5]thiadiazole</atitle><jtitle>Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003)</jtitle><date>2013-01-01</date><risdate>2013</risdate><volume>581</volume><issue>1</issue><spage>31</spage><epage>37</epage><pages>31-37</pages><issn>1542-1406</issn><eissn>1563-5287</eissn><abstract>A newly designed 2-arylbenzimidazole derivative which plays a role of co-acceptor unit has been prepared for the synthesis of conjugated polymer. 2-arylbenzimidazole derivative has been incorporated into 4,7-dithiophen-2-yl-benzo(2,1,3)thiadiazole (TBT) and fluorene based alternating copolymers with different ratios of 5 mol.% and 10 mol.% named POFTBT-IMD5, POFTBT-IMD10, respectively. We also synthesized alternating copolymer of 9,9-dioctylfluorene and TBT (POFTBT) to compare physical properties. POFTBT-IMD5, POFTBT-IMD10 films showed absorption peaks at 559 and 555 nm, respectively. The HOMO and LUMO energy levels of POFTBT-IMD5, POFTBT-IMD10 were −5.4/−3.84 eV and −5.4/−3.81 eV, respectively, which were similar to those of POFTBT (−5.3/−3.7 eV).</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/15421406.2013.808145</doi><tpages>7</tpages></addata></record> |
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subjects | 2-arylbenzimidazole benzothiadiazole conjugated polymer Copolymers Crystals Derivatives Energy levels Liquid crystals low band gap Physical properties Polymers Synthesis |
title | Synthesis and Characterization of π-Conjugated Polymers Based on 2-arylbenzimidazole and 4,7-di-thiophene-2-yl-4,5,6,7-tetrahydro-benzo[1,2,5]thiadiazole |
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