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Conducting Bipyridine-Bithiophene Copolymers
The synthesis and electrochemical polymerization of 6,6‘-bis(2‘‘-thienyl)-3,3‘-bipyridine (2) and 6,6‘-bis(2‘‘-thienyl)-2,2‘-bipyridine (3) are reported. Cyclic voltammetry shows that the resulting polymers have high bandgaps (3.0 and 3.2 eV, respectively) and are unstable in their p-doped (oxidized...
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Published in: | Chemistry of materials 1997-05, Vol.9 (5), p.1213-1216 |
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container_issue | 5 |
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container_title | Chemistry of materials |
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creator | Jenkins, Ieuan H Rees, Neale G Pickup, Peter G |
description | The synthesis and electrochemical polymerization of 6,6‘-bis(2‘‘-thienyl)-3,3‘-bipyridine (2) and 6,6‘-bis(2‘‘-thienyl)-2,2‘-bipyridine (3) are reported. Cyclic voltammetry shows that the resulting polymers have high bandgaps (3.0 and 3.2 eV, respectively) and are unstable in their p-doped (oxidized) states. Both polymers are stable when n-doped, but electronic conductivities determined by impedance spectroscopy were only ca. 3 × 10-8 S cm-2. Surprisingly, the greater conjugation in poly-2, which is demonstrated by its lower bandgap, does not lead to enhanced conductivity. |
doi_str_mv | 10.1021/cm960604v |
format | article |
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Cyclic voltammetry shows that the resulting polymers have high bandgaps (3.0 and 3.2 eV, respectively) and are unstable in their p-doped (oxidized) states. Both polymers are stable when n-doped, but electronic conductivities determined by impedance spectroscopy were only ca. 3 × 10-8 S cm-2. Surprisingly, the greater conjugation in poly-2, which is demonstrated by its lower bandgap, does not lead to enhanced conductivity.</description><identifier>ISSN: 0897-4756</identifier><identifier>EISSN: 1520-5002</identifier><identifier>DOI: 10.1021/cm960604v</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>Chemistry of materials, 1997-05, Vol.9 (5), p.1213-1216</ispartof><rights>Copyright © 1997 American Chemical Society</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-ac2182728dff8496e672c4da57c99e3a5731b160b04590078970583d1b5817513</citedby><cites>FETCH-LOGICAL-a324t-ac2182728dff8496e672c4da57c99e3a5731b160b04590078970583d1b5817513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2711619$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jenkins, Ieuan H</creatorcontrib><creatorcontrib>Rees, Neale G</creatorcontrib><creatorcontrib>Pickup, Peter G</creatorcontrib><title>Conducting Bipyridine-Bithiophene Copolymers</title><title>Chemistry of materials</title><addtitle>Chem. Mater</addtitle><description>The synthesis and electrochemical polymerization of 6,6‘-bis(2‘‘-thienyl)-3,3‘-bipyridine (2) and 6,6‘-bis(2‘‘-thienyl)-2,2‘-bipyridine (3) are reported. Cyclic voltammetry shows that the resulting polymers have high bandgaps (3.0 and 3.2 eV, respectively) and are unstable in their p-doped (oxidized) states. Both polymers are stable when n-doped, but electronic conductivities determined by impedance spectroscopy were only ca. 3 × 10-8 S cm-2. Surprisingly, the greater conjugation in poly-2, which is demonstrated by its lower bandgap, does not lead to enhanced conductivity.</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>0897-4756</issn><issn>1520-5002</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNptzz1PwzAQBmALgUQpDPyDDjAgYbhz4o-MEEEBVYBEUUfLdRzq0iaRnSL67wkK6sR0wz338RJyinCFwPDarjMBAtKvPTJAzoByALZPBqAySVPJxSE5inEJgB1XA3KZ11Wxsa2vPka3vtkGX_jK0VvfLnzdLFzlRnnd1Kvt2oV4TA5Ks4ru5K8Oyfv93TR_oJOX8WN-M6EmYWlLjWWomGSqKEuVZsIJyWxaGC5tlrmkqwnOUcAcUp4ByO414CopcM4VSo7JkFz0e22oYwyu1E3waxO2GkH_xtS7mJ09621jojWrMpjK-rgbYBJRYNYx2jMfW_e9a5vwqYVMJNfT1zedyKfZ82wMWnT-vPfGRr2sN6HqAv9z_gdr9mrp</recordid><startdate>19970515</startdate><enddate>19970515</enddate><creator>Jenkins, Ieuan H</creator><creator>Rees, Neale G</creator><creator>Pickup, Peter G</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19970515</creationdate><title>Conducting Bipyridine-Bithiophene Copolymers</title><author>Jenkins, Ieuan H ; Rees, Neale G ; Pickup, Peter G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-ac2182728dff8496e672c4da57c99e3a5731b160b04590078970583d1b5817513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</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>Jenkins, Ieuan H</creatorcontrib><creatorcontrib>Rees, Neale G</creatorcontrib><creatorcontrib>Pickup, Peter G</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Chemistry of materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jenkins, Ieuan H</au><au>Rees, Neale G</au><au>Pickup, Peter G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conducting Bipyridine-Bithiophene Copolymers</atitle><jtitle>Chemistry of materials</jtitle><addtitle>Chem. Mater</addtitle><date>1997-05-15</date><risdate>1997</risdate><volume>9</volume><issue>5</issue><spage>1213</spage><epage>1216</epage><pages>1213-1216</pages><issn>0897-4756</issn><eissn>1520-5002</eissn><abstract>The synthesis and electrochemical polymerization of 6,6‘-bis(2‘‘-thienyl)-3,3‘-bipyridine (2) and 6,6‘-bis(2‘‘-thienyl)-2,2‘-bipyridine (3) are reported. Cyclic voltammetry shows that the resulting polymers have high bandgaps (3.0 and 3.2 eV, respectively) and are unstable in their p-doped (oxidized) states. Both polymers are stable when n-doped, but electronic conductivities determined by impedance spectroscopy were only ca. 3 × 10-8 S cm-2. Surprisingly, the greater conjugation in poly-2, which is demonstrated by its lower bandgap, does not lead to enhanced conductivity.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/cm960604v</doi><tpages>4</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts |
title | Conducting Bipyridine-Bithiophene Copolymers |
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