Influence of Side-Chain Regiochemistry on the Transistor Performance of High-Mobility, All-Donor Polymers

Three novel polythiophene isomers are reported whereby the only difference in structure relates to the regiochemistry of the solubilizing side chains on the backbone. This is demonstrated to have a significant impact on the optoelectronic properties of the polymers and their propensity to aggregate...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the American Chemical Society 2014-10, Vol.136 (43), p.15154-15157
Hauptverfasser: Fei, Zhuping, Pattanasattayavong, Pichaya, Han, Yang, Schroeder, Bob C, Yan, Feng, Kline, R. Joseph, Anthopoulos, Thomas D, Heeney, Martin
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 15157
container_issue 43
container_start_page 15154
container_title Journal of the American Chemical Society
container_volume 136
creator Fei, Zhuping
Pattanasattayavong, Pichaya
Han, Yang
Schroeder, Bob C
Yan, Feng
Kline, R. Joseph
Anthopoulos, Thomas D
Heeney, Martin
description Three novel polythiophene isomers are reported whereby the only difference in structure relates to the regiochemistry of the solubilizing side chains on the backbone. This is demonstrated to have a significant impact on the optoelectronic properties of the polymers and their propensity to aggregate in solution. These differences are rationalized on the basis of differences in backbone torsion. The polymer with the largest effective conjugation length is demonstrated to exhibit the highest field-effect mobility, with peak values up to 4.6 cm2 V–1 s–1.
doi_str_mv 10.1021/ja508798s
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1618828544</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1618828544</sourcerecordid><originalsourceid>FETCH-LOGICAL-a416t-a67b16f3707bc1509339f50a07d91b69e7b3ccbcb19610ac1452dea47adc58403</originalsourceid><addsrcrecordid>eNptkF1LwzAUhoMobk4v_APSG0HBaJImTXs55scGE0XndUnSdM1Im5m0F_33dmx65dXhHJ7zwvsAcInRPUYEP2wEQynP0nAExpgRBBkmyTEYI4QI5GkSj8BZCJthpSTFp2BEWIwI5XQMzKIpbacbpSNXRp-m0HBWCdNEH3ptnKp0bULr-8g1UVvpaOVFE4aL89G79qXztTi8zs26gq9OGmva_i6aWgsfXbPjnO1r7cM5OCmFDfriMCfg6_lpNZvD5dvLYjZdQkFx0kKRcImTMuaIS4UZyuI4KxkSiBcZlkmmuYyVkkriLMFIKEwZKbSgXBSKpRTFE3Czz916993p0OZDBaWtFY12XchxgtOUpIzSAb3do8q7ELwu8603tfB9jlG-M5v_mR3Yq0NsJ2td_JG_Kgfgeg8IFfKN63wztPwn6AcaVn-g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1618828544</pqid></control><display><type>article</type><title>Influence of Side-Chain Regiochemistry on the Transistor Performance of High-Mobility, All-Donor Polymers</title><source>ACS Publications</source><creator>Fei, Zhuping ; Pattanasattayavong, Pichaya ; Han, Yang ; Schroeder, Bob C ; Yan, Feng ; Kline, R. Joseph ; Anthopoulos, Thomas D ; Heeney, Martin</creator><creatorcontrib>Fei, Zhuping ; Pattanasattayavong, Pichaya ; Han, Yang ; Schroeder, Bob C ; Yan, Feng ; Kline, R. Joseph ; Anthopoulos, Thomas D ; Heeney, Martin</creatorcontrib><description>Three novel polythiophene isomers are reported whereby the only difference in structure relates to the regiochemistry of the solubilizing side chains on the backbone. This is demonstrated to have a significant impact on the optoelectronic properties of the polymers and their propensity to aggregate in solution. These differences are rationalized on the basis of differences in backbone torsion. The polymer with the largest effective conjugation length is demonstrated to exhibit the highest field-effect mobility, with peak values up to 4.6 cm2 V–1 s–1.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja508798s</identifier><identifier>PMID: 25302474</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Journal of the American Chemical Society, 2014-10, Vol.136 (43), p.15154-15157</ispartof><rights>Copyright © 2014 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a416t-a67b16f3707bc1509339f50a07d91b69e7b3ccbcb19610ac1452dea47adc58403</citedby><cites>FETCH-LOGICAL-a416t-a67b16f3707bc1509339f50a07d91b69e7b3ccbcb19610ac1452dea47adc58403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja508798s$$EPDF$$P50$$Gacs$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja508798s$$EHTML$$P50$$Gacs$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25302474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fei, Zhuping</creatorcontrib><creatorcontrib>Pattanasattayavong, Pichaya</creatorcontrib><creatorcontrib>Han, Yang</creatorcontrib><creatorcontrib>Schroeder, Bob C</creatorcontrib><creatorcontrib>Yan, Feng</creatorcontrib><creatorcontrib>Kline, R. Joseph</creatorcontrib><creatorcontrib>Anthopoulos, Thomas D</creatorcontrib><creatorcontrib>Heeney, Martin</creatorcontrib><title>Influence of Side-Chain Regiochemistry on the Transistor Performance of High-Mobility, All-Donor Polymers</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Three novel polythiophene isomers are reported whereby the only difference in structure relates to the regiochemistry of the solubilizing side chains on the backbone. This is demonstrated to have a significant impact on the optoelectronic properties of the polymers and their propensity to aggregate in solution. These differences are rationalized on the basis of differences in backbone torsion. The polymer with the largest effective conjugation length is demonstrated to exhibit the highest field-effect mobility, with peak values up to 4.6 cm2 V–1 s–1.</description><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>N~.</sourceid><recordid>eNptkF1LwzAUhoMobk4v_APSG0HBaJImTXs55scGE0XndUnSdM1Im5m0F_33dmx65dXhHJ7zwvsAcInRPUYEP2wEQynP0nAExpgRBBkmyTEYI4QI5GkSj8BZCJthpSTFp2BEWIwI5XQMzKIpbacbpSNXRp-m0HBWCdNEH3ptnKp0bULr-8g1UVvpaOVFE4aL89G79qXztTi8zs26gq9OGmva_i6aWgsfXbPjnO1r7cM5OCmFDfriMCfg6_lpNZvD5dvLYjZdQkFx0kKRcImTMuaIS4UZyuI4KxkSiBcZlkmmuYyVkkriLMFIKEwZKbSgXBSKpRTFE3Czz916993p0OZDBaWtFY12XchxgtOUpIzSAb3do8q7ELwu8603tfB9jlG-M5v_mR3Yq0NsJ2td_JG_Kgfgeg8IFfKN63wztPwn6AcaVn-g</recordid><startdate>20141029</startdate><enddate>20141029</enddate><creator>Fei, Zhuping</creator><creator>Pattanasattayavong, Pichaya</creator><creator>Han, Yang</creator><creator>Schroeder, Bob C</creator><creator>Yan, Feng</creator><creator>Kline, R. Joseph</creator><creator>Anthopoulos, Thomas D</creator><creator>Heeney, Martin</creator><general>American Chemical Society</general><scope>N~.</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20141029</creationdate><title>Influence of Side-Chain Regiochemistry on the Transistor Performance of High-Mobility, All-Donor Polymers</title><author>Fei, Zhuping ; Pattanasattayavong, Pichaya ; Han, Yang ; Schroeder, Bob C ; Yan, Feng ; Kline, R. Joseph ; Anthopoulos, Thomas D ; Heeney, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a416t-a67b16f3707bc1509339f50a07d91b69e7b3ccbcb19610ac1452dea47adc58403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fei, Zhuping</creatorcontrib><creatorcontrib>Pattanasattayavong, Pichaya</creatorcontrib><creatorcontrib>Han, Yang</creatorcontrib><creatorcontrib>Schroeder, Bob C</creatorcontrib><creatorcontrib>Yan, Feng</creatorcontrib><creatorcontrib>Kline, R. Joseph</creatorcontrib><creatorcontrib>Anthopoulos, Thomas D</creatorcontrib><creatorcontrib>Heeney, Martin</creatorcontrib><collection>American Chemical Society (ACS) Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fei, Zhuping</au><au>Pattanasattayavong, Pichaya</au><au>Han, Yang</au><au>Schroeder, Bob C</au><au>Yan, Feng</au><au>Kline, R. Joseph</au><au>Anthopoulos, Thomas D</au><au>Heeney, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Side-Chain Regiochemistry on the Transistor Performance of High-Mobility, All-Donor Polymers</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2014-10-29</date><risdate>2014</risdate><volume>136</volume><issue>43</issue><spage>15154</spage><epage>15157</epage><pages>15154-15157</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Three novel polythiophene isomers are reported whereby the only difference in structure relates to the regiochemistry of the solubilizing side chains on the backbone. This is demonstrated to have a significant impact on the optoelectronic properties of the polymers and their propensity to aggregate in solution. These differences are rationalized on the basis of differences in backbone torsion. The polymer with the largest effective conjugation length is demonstrated to exhibit the highest field-effect mobility, with peak values up to 4.6 cm2 V–1 s–1.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25302474</pmid><doi>10.1021/ja508798s</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0002-7863
ispartof Journal of the American Chemical Society, 2014-10, Vol.136 (43), p.15154-15157
issn 0002-7863
1520-5126
language eng
recordid cdi_proquest_miscellaneous_1618828544
source ACS Publications
title Influence of Side-Chain Regiochemistry on the Transistor Performance of High-Mobility, All-Donor Polymers
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T03%3A39%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Influence%20of%20Side-Chain%20Regiochemistry%20on%20the%20Transistor%20Performance%20of%20High-Mobility,%20All-Donor%20Polymers&rft.jtitle=Journal%20of%20the%20American%20Chemical%20Society&rft.au=Fei,%20Zhuping&rft.date=2014-10-29&rft.volume=136&rft.issue=43&rft.spage=15154&rft.epage=15157&rft.pages=15154-15157&rft.issn=0002-7863&rft.eissn=1520-5126&rft_id=info:doi/10.1021/ja508798s&rft_dat=%3Cproquest_cross%3E1618828544%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1618828544&rft_id=info:pmid/25302474&rfr_iscdi=true