Donor–Acceptor Conjugated Polymers Based on p- and o-Benzodifuranone and Thiophene Derivatives: Electrochemical Preparation and Optical and Electronic Properties
A series of π-conjugated polymers consisting of bis-EDOT or bis-EDTT units and p- or o-diphenylbenzodifuranones have been prepared electrochemically. The monomers and polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. The monomers were synthesized from 3,4-ethyle...
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Veröffentlicht in: | Macromolecules 2012-01, Vol.45 (2), p.743-750 |
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creator | Zhang, Kai Tieke, Bernd Forgie, John C Vilela, Filipe Skabara, Peter J |
description | A series of π-conjugated polymers consisting of bis-EDOT or bis-EDTT units and p- or o-diphenylbenzodifuranones have been prepared electrochemically. The monomers and polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. The monomers were synthesized from 3,4-ethylenedioxythien-2-yl or 3,4-ethylenedithiathien-2-yl trimethylstannane and 3,7-bis(4-bromophenyl)benzo[1,2-b:4,5-b′]difuran-2,6-dione or 3,6-bis(4-bromophenyl)benzo[1,2-b:6,5-b′]difuran-2,7-dione using Stille coupling. The polymers exhibit broad absorption bands, and strong donor–acceptor characteristics with very small band gaps (in a range from 0.40 to 1.20 eV). Electrochemically grown polymer thin films exhibit reversible behavior under oxidative and reductive conditions. Under reduction, the polymer films show color changes from dark to almost transparent. |
doi_str_mv | 10.1021/ma202387t |
format | Article |
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The monomers and polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. The monomers were synthesized from 3,4-ethylenedioxythien-2-yl or 3,4-ethylenedithiathien-2-yl trimethylstannane and 3,7-bis(4-bromophenyl)benzo[1,2-b:4,5-b′]difuran-2,6-dione or 3,6-bis(4-bromophenyl)benzo[1,2-b:6,5-b′]difuran-2,7-dione using Stille coupling. The polymers exhibit broad absorption bands, and strong donor–acceptor characteristics with very small band gaps (in a range from 0.40 to 1.20 eV). Electrochemically grown polymer thin films exhibit reversible behavior under oxidative and reductive conditions. Under reduction, the polymer films show color changes from dark to almost transparent.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma202387t</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Physicochemistry of polymers ; Polymerization ; Polymers and radiations</subject><ispartof>Macromolecules, 2012-01, Vol.45 (2), p.743-750</ispartof><rights>Copyright © 2011 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a355t-501ac3641d085c8dcf5cf39b306cf0087d3793306b4cbb476afe7350b7191e343</citedby><cites>FETCH-LOGICAL-a355t-501ac3641d085c8dcf5cf39b306cf0087d3793306b4cbb476afe7350b7191e343</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/ma202387t$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma202387t$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2764,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25476022$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Kai</creatorcontrib><creatorcontrib>Tieke, Bernd</creatorcontrib><creatorcontrib>Forgie, John C</creatorcontrib><creatorcontrib>Vilela, Filipe</creatorcontrib><creatorcontrib>Skabara, Peter J</creatorcontrib><title>Donor–Acceptor Conjugated Polymers Based on p- and o-Benzodifuranone and Thiophene Derivatives: Electrochemical Preparation and Optical and Electronic Properties</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>A series of π-conjugated polymers consisting of bis-EDOT or bis-EDTT units and p- or o-diphenylbenzodifuranones have been prepared electrochemically. The monomers and polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. The monomers were synthesized from 3,4-ethylenedioxythien-2-yl or 3,4-ethylenedithiathien-2-yl trimethylstannane and 3,7-bis(4-bromophenyl)benzo[1,2-b:4,5-b′]difuran-2,6-dione or 3,6-bis(4-bromophenyl)benzo[1,2-b:6,5-b′]difuran-2,7-dione using Stille coupling. The polymers exhibit broad absorption bands, and strong donor–acceptor characteristics with very small band gaps (in a range from 0.40 to 1.20 eV). Electrochemically grown polymer thin films exhibit reversible behavior under oxidative and reductive conditions. Under reduction, the polymer films show color changes from dark to almost transparent.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Physicochemistry of polymers</subject><subject>Polymerization</subject><subject>Polymers and radiations</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNptkEtOwzAQhi0EEqWw4AbZsGAR8CNuEnZ98ZAqtYuyjhxnQl2ldmS7lcqKO3AEbsZJcB-CDauZf-abX_aP0DXBdwRTcr8SFFOWpf4EdQinOOYZ46eogzFN4pzm6Tm6cG6JMSE8YR30NTLa2O-Pz76U0Hpjo6HRy_Wb8FBFM9NsV2BdNBAuSKOjNo6EDl08AP1uKlWvrdBGw346XyjTLiCoEVi1EV5twD1E4wakt0YuYKWkaKKZhVbYsA1-u7Np6_fzXX9ktZIBMy1Yr8BdorNaNA6ujrWLXh_H8-FzPJk-vQz7k1gwzn3MMRGS9RJS4YzLrJI1lzXLS4Z7ssY4SyuW5iyoMpFlmaQ9UUPKOC5TkhNgCeui24OvtMY5C3XRWrUSdlsQXOzSLX7TDezNgW2FC4-vQwxSud8DyoM_pvSPE9IVS7O2OvzgH78fAF2J1w</recordid><startdate>20120124</startdate><enddate>20120124</enddate><creator>Zhang, Kai</creator><creator>Tieke, Bernd</creator><creator>Forgie, John C</creator><creator>Vilela, Filipe</creator><creator>Skabara, Peter J</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20120124</creationdate><title>Donor–Acceptor Conjugated Polymers Based on p- and o-Benzodifuranone and Thiophene Derivatives: Electrochemical Preparation and Optical and Electronic Properties</title><author>Zhang, Kai ; Tieke, Bernd ; Forgie, John C ; Vilela, Filipe ; Skabara, Peter J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a355t-501ac3641d085c8dcf5cf39b306cf0087d3793306b4cbb476afe7350b7191e343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Physicochemistry of polymers</topic><topic>Polymerization</topic><topic>Polymers and radiations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Kai</creatorcontrib><creatorcontrib>Tieke, Bernd</creatorcontrib><creatorcontrib>Forgie, John C</creatorcontrib><creatorcontrib>Vilela, Filipe</creatorcontrib><creatorcontrib>Skabara, Peter J</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Kai</au><au>Tieke, Bernd</au><au>Forgie, John C</au><au>Vilela, Filipe</au><au>Skabara, Peter J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Donor–Acceptor Conjugated Polymers Based on p- and o-Benzodifuranone and Thiophene Derivatives: Electrochemical Preparation and Optical and Electronic Properties</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2012-01-24</date><risdate>2012</risdate><volume>45</volume><issue>2</issue><spage>743</spage><epage>750</epage><pages>743-750</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>A series of π-conjugated polymers consisting of bis-EDOT or bis-EDTT units and p- or o-diphenylbenzodifuranones have been prepared electrochemically. The monomers and polymers were investigated using UV/vis absorption spectroscopy and cyclic voltammetry. The monomers were synthesized from 3,4-ethylenedioxythien-2-yl or 3,4-ethylenedithiathien-2-yl trimethylstannane and 3,7-bis(4-bromophenyl)benzo[1,2-b:4,5-b′]difuran-2,6-dione or 3,6-bis(4-bromophenyl)benzo[1,2-b:6,5-b′]difuran-2,7-dione using Stille coupling. The polymers exhibit broad absorption bands, and strong donor–acceptor characteristics with very small band gaps (in a range from 0.40 to 1.20 eV). Electrochemically grown polymer thin films exhibit reversible behavior under oxidative and reductive conditions. Under reduction, the polymer films show color changes from dark to almost transparent.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma202387t</doi><tpages>8</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Physicochemistry of polymers Polymerization Polymers and radiations |
title | Donor–Acceptor Conjugated Polymers Based on p- and o-Benzodifuranone and Thiophene Derivatives: Electrochemical Preparation and Optical and Electronic Properties |
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