Spray Coatable Electrochromic Dioxythiophene Polymers with High Coloration Efficiencies
Four new disubstituted propylenedioxythiophene polymers have been synthesized by Grignard metathesis on the 1−5 g scale. All polymers were found to be soluble in chloroform, methylene chloride, toluene, and tetrahydrofuran and were fully structurally characterized having GPC determined number-averag...
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Veröffentlicht in: | Macromolecules 2004-10, Vol.37 (20), p.7559-7569 |
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description | Four new disubstituted propylenedioxythiophene polymers have been synthesized by Grignard metathesis on the 1−5 g scale. All polymers were found to be soluble in chloroform, methylene chloride, toluene, and tetrahydrofuran and were fully structurally characterized having GPC determined number-average molecular weights ranging from 33000 to 47000 g mol-1. Dilute polymer solutions in toluene exhibited strong red fluorescence with moderate quantum efficiencies from 0.38 to 0.50. Homogeneous thin films were formed by electropolymerization and spray casting polymer solutions onto ITO coated glass slides at thicknesses of ca. 150 nm. The films were electroactive, switching from a dark blue-purple to a transmissive sky blue upon p-doping, often with subsecond switching times, and high electrochromic contrast luminance changes (% ΔY) of 40−70%. These studies revealed that the branched derivatives, [poly(3,3-bis(2-ethylhexyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(6,8-dibromo-3,3-bis(2-ethylhexyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)], gave an electrochemical response and associated color change over a much smaller voltage range in comparison to the linear chain substituted derivatives, [poly(3,3-dihexyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(3,3-bis(octadecyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)]. Composite coloration efficiency values were found up to 1365 cm2/C; this was considerably larger than values obtained from previously studied alkylenedioxythiophene based polymers (∼375 cm2/C). |
doi_str_mv | 10.1021/ma049222y |
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G ; Argun, Avni A ; Cirpan, Ali ; McCarley, Tracy D ; Reynolds, John R</creator><creatorcontrib>Reeves, Benjamin D ; Grenier, Christophe R. G ; Argun, Avni A ; Cirpan, Ali ; McCarley, Tracy D ; Reynolds, John R</creatorcontrib><description>Four new disubstituted propylenedioxythiophene polymers have been synthesized by Grignard metathesis on the 1−5 g scale. All polymers were found to be soluble in chloroform, methylene chloride, toluene, and tetrahydrofuran and were fully structurally characterized having GPC determined number-average molecular weights ranging from 33000 to 47000 g mol-1. Dilute polymer solutions in toluene exhibited strong red fluorescence with moderate quantum efficiencies from 0.38 to 0.50. Homogeneous thin films were formed by electropolymerization and spray casting polymer solutions onto ITO coated glass slides at thicknesses of ca. 150 nm. The films were electroactive, switching from a dark blue-purple to a transmissive sky blue upon p-doping, often with subsecond switching times, and high electrochromic contrast luminance changes (% ΔY) of 40−70%. These studies revealed that the branched derivatives, [poly(3,3-bis(2-ethylhexyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(6,8-dibromo-3,3-bis(2-ethylhexyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)], gave an electrochemical response and associated color change over a much smaller voltage range in comparison to the linear chain substituted derivatives, [poly(3,3-dihexyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(3,3-bis(octadecyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)]. Composite coloration efficiency values were found up to 1365 cm2/C; this was considerably larger than values obtained from previously studied alkylenedioxythiophene based polymers (∼375 cm2/C).</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma049222y</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Macromolecules, 2004-10, Vol.37 (20), p.7559-7569</ispartof><rights>Copyright © 2004 American Chemical Society</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a287t-2aaf3d294137d5faa67b243f5d2fbae599b8e6d953ae82a1bb4ecb0082cf880d3</citedby><cites>FETCH-LOGICAL-a287t-2aaf3d294137d5faa67b243f5d2fbae599b8e6d953ae82a1bb4ecb0082cf880d3</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/ma049222y$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma049222y$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27081,27929,27930,56743,56793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16160332$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Reeves, Benjamin D</creatorcontrib><creatorcontrib>Grenier, Christophe R. G</creatorcontrib><creatorcontrib>Argun, Avni A</creatorcontrib><creatorcontrib>Cirpan, Ali</creatorcontrib><creatorcontrib>McCarley, Tracy D</creatorcontrib><creatorcontrib>Reynolds, John R</creatorcontrib><title>Spray Coatable Electrochromic Dioxythiophene Polymers with High Coloration Efficiencies</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Four new disubstituted propylenedioxythiophene polymers have been synthesized by Grignard metathesis on the 1−5 g scale. All polymers were found to be soluble in chloroform, methylene chloride, toluene, and tetrahydrofuran and were fully structurally characterized having GPC determined number-average molecular weights ranging from 33000 to 47000 g mol-1. Dilute polymer solutions in toluene exhibited strong red fluorescence with moderate quantum efficiencies from 0.38 to 0.50. Homogeneous thin films were formed by electropolymerization and spray casting polymer solutions onto ITO coated glass slides at thicknesses of ca. 150 nm. The films were electroactive, switching from a dark blue-purple to a transmissive sky blue upon p-doping, often with subsecond switching times, and high electrochromic contrast luminance changes (% ΔY) of 40−70%. These studies revealed that the branched derivatives, [poly(3,3-bis(2-ethylhexyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(6,8-dibromo-3,3-bis(2-ethylhexyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)], gave an electrochemical response and associated color change over a much smaller voltage range in comparison to the linear chain substituted derivatives, [poly(3,3-dihexyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(3,3-bis(octadecyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)]. Composite coloration efficiency values were found up to 1365 cm2/C; this was considerably larger than values obtained from previously studied alkylenedioxythiophene based polymers (∼375 cm2/C).</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNptkE9LxDAUxIMoWFcPfoNcPHioJi9N_xxlXV1hQUHFY3lNE5ulbUpS0X57KyvuxcPwLr8Z3gwh55xdcQb8ukOWFAAwHZCIS2CxzIU8JBFjkMQFFNkxOQlhyxjnMhEReXsePE506XDEqtV01Wo1eqca7zqr6K11X9PYWDc0utf0ybVTp32gn3Zs6Nq-N7OzdR5H63q6MsYqq_tZ4ZQcGWyDPvu9C_J6t3pZruPN4_3D8mYTI-TZGAOiETUUCRdZLQ1imlWQCCNrMBVqWRRVrtO6kAJ1DsirKtGqYiwHZfKc1WJBLne5yrsQvDbl4G2Hfio5K38WKf8WmdmLHTtgUNgaj_OrYW9IecqEgD2HKpRb9-H7ucE_ed-0mG6B</recordid><startdate>20041005</startdate><enddate>20041005</enddate><creator>Reeves, Benjamin D</creator><creator>Grenier, Christophe R. G</creator><creator>Argun, Avni A</creator><creator>Cirpan, Ali</creator><creator>McCarley, Tracy D</creator><creator>Reynolds, John R</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20041005</creationdate><title>Spray Coatable Electrochromic Dioxythiophene Polymers with High Coloration Efficiencies</title><author>Reeves, Benjamin D ; Grenier, Christophe R. G ; Argun, Avni A ; Cirpan, Ali ; McCarley, Tracy D ; Reynolds, John R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a287t-2aaf3d294137d5faa67b243f5d2fbae599b8e6d953ae82a1bb4ecb0082cf880d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reeves, Benjamin D</creatorcontrib><creatorcontrib>Grenier, Christophe R. G</creatorcontrib><creatorcontrib>Argun, Avni A</creatorcontrib><creatorcontrib>Cirpan, Ali</creatorcontrib><creatorcontrib>McCarley, Tracy D</creatorcontrib><creatorcontrib>Reynolds, John R</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reeves, Benjamin D</au><au>Grenier, Christophe R. G</au><au>Argun, Avni A</au><au>Cirpan, Ali</au><au>McCarley, Tracy D</au><au>Reynolds, John R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spray Coatable Electrochromic Dioxythiophene Polymers with High Coloration Efficiencies</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2004-10-05</date><risdate>2004</risdate><volume>37</volume><issue>20</issue><spage>7559</spage><epage>7569</epage><pages>7559-7569</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Four new disubstituted propylenedioxythiophene polymers have been synthesized by Grignard metathesis on the 1−5 g scale. All polymers were found to be soluble in chloroform, methylene chloride, toluene, and tetrahydrofuran and were fully structurally characterized having GPC determined number-average molecular weights ranging from 33000 to 47000 g mol-1. Dilute polymer solutions in toluene exhibited strong red fluorescence with moderate quantum efficiencies from 0.38 to 0.50. Homogeneous thin films were formed by electropolymerization and spray casting polymer solutions onto ITO coated glass slides at thicknesses of ca. 150 nm. The films were electroactive, switching from a dark blue-purple to a transmissive sky blue upon p-doping, often with subsecond switching times, and high electrochromic contrast luminance changes (% ΔY) of 40−70%. These studies revealed that the branched derivatives, [poly(3,3-bis(2-ethylhexyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(6,8-dibromo-3,3-bis(2-ethylhexyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)], gave an electrochemical response and associated color change over a much smaller voltage range in comparison to the linear chain substituted derivatives, [poly(3,3-dihexyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)] and [poly(3,3-bis(octadecyloxymethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine)]. Composite coloration efficiency values were found up to 1365 cm2/C; this was considerably larger than values obtained from previously studied alkylenedioxythiophene based polymers (∼375 cm2/C).</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma049222y</doi><tpages>11</tpages></addata></record> |
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title | Spray Coatable Electrochromic Dioxythiophene Polymers with High Coloration Efficiencies |
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