Synthesis and Characterization of Regioregular Polymers Containing Substituted Thienylene/Bithienylene and Phenylene Repeating Units

Regioregular polymers poly(3-alkyl-2,5-thienylene-alt-1,4-phenylene) (PBTC n , n = 4, 8, 12) and poly[1,4-bis(3-alkyl-2-thienyl)phenylene] (PBTBC n , n = 4, 8, 12), which contain alternating phenylene and substituted thienylene or bithienylene repeating units, have been chemically and/or electrochem...

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Veröffentlicht in:Macromolecules 2000-10, Vol.33 (20), p.7349-7358
Hauptverfasser: Ng, S. C, Xu, J. M, Chan, Hardy S. O
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container_title Macromolecules
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creator Ng, S. C
Xu, J. M
Chan, Hardy S. O
description Regioregular polymers poly(3-alkyl-2,5-thienylene-alt-1,4-phenylene) (PBTC n , n = 4, 8, 12) and poly[1,4-bis(3-alkyl-2-thienyl)phenylene] (PBTBC n , n = 4, 8, 12), which contain alternating phenylene and substituted thienylene or bithienylene repeating units, have been chemically and/or electrochemically synthesized and characterized. Their structures are consistent with that expected as indicated by NMR, FTIR, and microanalysis. The change in glass transition temperature and UV−vis and fluorescence spectra with modification of polymer backbone and increase of the alkyl chain length has been observed and discussed. The PBTC n series shows better thermal stability in air, and the compounds in the series are partially crystalline. The PBTC n polymers have liquid crystalline properties as shown by MDSC, XRD, and polarized optical microscopy. XPS study performed on both the neutral and doped states shows the formation of charge carrier in the polymer backbone when doped. The polymers are both p- and n-dopable as indicated by cyclic voltammetry. Electrochromism when the polymers are p-doped is also evidenced by the spectral changes in UV−vis−NIR region.
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XPS study performed on both the neutral and doped states shows the formation of charge carrier in the polymer backbone when doped. The polymers are both p- and n-dopable as indicated by cyclic voltammetry. 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The PBTC n series shows better thermal stability in air, and the compounds in the series are partially crystalline. The PBTC n polymers have liquid crystalline properties as shown by MDSC, XRD, and polarized optical microscopy. XPS study performed on both the neutral and doped states shows the formation of charge carrier in the polymer backbone when doped. The polymers are both p- and n-dopable as indicated by cyclic voltammetry. Electrochromism when the polymers are p-doped is also evidenced by the spectral changes in UV−vis−NIR region.</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>2000</creationdate><recordtype>article</recordtype><recordid>eNptkEtPwzAQhC0EEqVw4B_kAAcOobbzPkJ5q4jStGdrk6xbQ-pUtiNRzvxwAoVy4bQa7Tez2iHkmNFzRjkbLCHLOKXU7ZAeizj1ozSIdkmPUh76Gc-SfXJg7QuljEVh0CMf-Vq7BVplPdCVN1yAgdKhUe_gVKO9RnoTnKvG4LytwXjjpl4v0Vhv2GgHSis99_K2sE651mHlTRcK9bpGjYNL5bbiO3y8-FUTXGGX33lnWjl7SPYk1BaPfmafzG6up8M7f_R0ez-8GPkQZNT5VVqGccAxAJ5RqAqWYChpgbFkFFOsIJEpFknGZURRZmXIMWW8iFjY8WFZBX1ytsktTWOtQSlWRi3BrAWj4qs-sa2vY0827ApsCbU0oEtl_wwRS2MWdJi_wZR1-LZdg3kVcRIkkZiOc5E_Xj3zUfIgeMefbngorXhpWqO7h_85_wmdwY6G</recordid><startdate>20001003</startdate><enddate>20001003</enddate><creator>Ng, S. 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O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a390t-d8c4632e3a290adb17e4f0be6f10e8eda7f8eb792f50ef9c42e812b5142904cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</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>Ng, S. C</creatorcontrib><creatorcontrib>Xu, J. M</creatorcontrib><creatorcontrib>Chan, Hardy S. 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The change in glass transition temperature and UV−vis and fluorescence spectra with modification of polymer backbone and increase of the alkyl chain length has been observed and discussed. The PBTC n series shows better thermal stability in air, and the compounds in the series are partially crystalline. The PBTC n polymers have liquid crystalline properties as shown by MDSC, XRD, and polarized optical microscopy. XPS study performed on both the neutral and doped states shows the formation of charge carrier in the polymer backbone when doped. The polymers are both p- and n-dopable as indicated by cyclic voltammetry. Electrochromism when the polymers are p-doped is also evidenced by the spectral changes in UV−vis−NIR region.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma992000t</doi><tpages>10</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 Synthesis and Characterization of Regioregular Polymers Containing Substituted Thienylene/Bithienylene and Phenylene Repeating Units
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