CHAPTER 9 - Polythiophenes
Identifieur interne : 004517 ( Main/Exploration ); précédent : 004516; suivant : 004518CHAPTER 9 - Polythiophenes
Auteurs : Dahlia Haynes [États-Unis] ; Richard Mccullough [États-Unis]Source :
- RSC Polymer Chemistry Series [ 2044-0790 ]
Descripteurs français
- Wicri :
- topic : Polymère.
English descriptors
- KwdEn :
- Catalyst, Chcl3, Chem, Commun, Ether, Experimental procedures, Fecl3, Grignard, Hexane, Ltered, Macromolecule, Mater, Mccullough, Mccullough method, Meoh, Mmol, Molecular weights, Monomer, Nonsubstituted, Nonsubstituted polythiophenes, P3ats, Polym, Polymer, Polymerization, Polystyrene standards, Polythiophene, Polythiophenes, Quenched, Reaction mixture, Regioregular, Regioregular polythiophenes, Rieke, Soxhlet, Soxhlet extractions, Soxhlet thimble, Synth, Synthetic method, Synthetic methods, Synthetic procedures, Thiophene, Thiophene monomers.
- Teeft :
- Catalyst, Chcl3, Chem, Commun, Ether, Experimental procedures, Fecl3, Grignard, Hexane, Ltered, Macromolecule, Mater, Mccullough, Mccullough method, Meoh, Mmol, Molecular weights, Monomer, Nonsubstituted, Nonsubstituted polythiophenes, P3ats, Polym, Polymer, Polymerization, Polystyrene standards, Polythiophene, Polythiophenes, Quenched, Reaction mixture, Regioregular, Regioregular polythiophenes, Rieke, Soxhlet, Soxhlet extractions, Soxhlet thimble, Synth, Synthetic method, Synthetic methods, Synthetic procedures, Thiophene, Thiophene monomers.
Abstract
Conjugated polymers have garnered a surplus of attention ever since the discovery of their promising and diverse electrical and optical properties. Thus, the term “organic electronics” has arisen due to the vast amount of interest in semiconductor polymeric materials. Of this conjugated polymers family, Polythiophenes and their derivatives remain one of the most highly researched in the “organic electronics” area. Their solubility, processability, high conductivity, low cost and ease of synthesis offer an attractive route towards modifiable semiconductors that can be tailored for specific applications. This chapter will delve into the history of polythiophenes with emphasis on polymerization techniques and synthetic experimental details.
Url:
DOI: 10.1039/9781849739771-00180
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001E75
- to stream Istex, to step Curation: 001E75
- to stream Istex, to step Checkpoint: 000019
- to stream Main, to step Merge: 004748
- to stream Main, to step Curation: 004517
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title>CHAPTER 9 - Polythiophenes</title>
<author><name sortKey="Haynes, Dahlia" sort="Haynes, Dahlia" uniqKey="Haynes D" first="Dahlia" last="Haynes">Dahlia Haynes</name>
</author>
<author><name sortKey="Mccullough, Richard" sort="Mccullough, Richard" uniqKey="Mccullough R" first="Richard" last="Mccullough">Richard Mccullough</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:84C4226EB7729DC751C30AC714D830E327E0913B</idno>
<date when="2014" year="2014">2014</date>
<idno type="doi">10.1039/9781849739771-00180</idno>
<idno type="url">https://api.istex.fr/document/84C4226EB7729DC751C30AC714D830E327E0913B/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001E75</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001E75</idno>
<idno type="wicri:Area/Istex/Curation">001E75</idno>
<idno type="wicri:Area/Istex/Checkpoint">000019</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000019</idno>
<idno type="wicri:Area/Main/Merge">004748</idno>
<idno type="wicri:Area/Main/Curation">004517</idno>
<idno type="wicri:Area/Main/Exploration">004517</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a">CHAPTER 9 - Polythiophenes</title>
<author><name sortKey="Haynes, Dahlia" sort="Haynes, Dahlia" uniqKey="Haynes D" first="Dahlia" last="Haynes">Dahlia Haynes</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<placeName><region type="state">Pennsylvanie</region>
</placeName>
<wicri:cityArea>a Carnegie Mellon University Department of Chemistry, Mellon Institute</wicri:cityArea>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>b Harvard University 1350 Massachusetts Avenue, Holyoke Center, Suite 836, Cambridge</wicri:regionArea>
<wicri:noRegion>Cambridge</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country wicri:rule="url">États-Unis</country>
</affiliation>
</author>
<author><name sortKey="Mccullough, Richard" sort="Mccullough, Richard" uniqKey="Mccullough R" first="Richard" last="Mccullough">Richard Mccullough</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<placeName><region type="state">Pennsylvanie</region>
</placeName>
<wicri:cityArea>a Carnegie Mellon University Department of Chemistry, Mellon Institute</wicri:cityArea>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>b Harvard University 1350 Massachusetts Avenue, Holyoke Center, Suite 836, Cambridge</wicri:regionArea>
<wicri:noRegion>Cambridge</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country wicri:rule="url">États-Unis</country>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="s">RSC Polymer Chemistry Series</title>
<idno type="ISSN">2044-0790</idno>
<idno type="eISSN">2044-0804</idno>
<idno type="ISSN">2044-0790</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">2044-0790</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Catalyst</term>
<term>Chcl3</term>
<term>Chem</term>
<term>Commun</term>
<term>Ether</term>
<term>Experimental procedures</term>
<term>Fecl3</term>
<term>Grignard</term>
<term>Hexane</term>
<term>Ltered</term>
<term>Macromolecule</term>
<term>Mater</term>
<term>Mccullough</term>
<term>Mccullough method</term>
<term>Meoh</term>
<term>Mmol</term>
<term>Molecular weights</term>
<term>Monomer</term>
<term>Nonsubstituted</term>
<term>Nonsubstituted polythiophenes</term>
<term>P3ats</term>
<term>Polym</term>
<term>Polymer</term>
<term>Polymerization</term>
<term>Polystyrene standards</term>
<term>Polythiophene</term>
<term>Polythiophenes</term>
<term>Quenched</term>
<term>Reaction mixture</term>
<term>Regioregular</term>
<term>Regioregular polythiophenes</term>
<term>Rieke</term>
<term>Soxhlet</term>
<term>Soxhlet extractions</term>
<term>Soxhlet thimble</term>
<term>Synth</term>
<term>Synthetic method</term>
<term>Synthetic methods</term>
<term>Synthetic procedures</term>
<term>Thiophene</term>
<term>Thiophene monomers</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Catalyst</term>
<term>Chcl3</term>
<term>Chem</term>
<term>Commun</term>
<term>Ether</term>
<term>Experimental procedures</term>
<term>Fecl3</term>
<term>Grignard</term>
<term>Hexane</term>
<term>Ltered</term>
<term>Macromolecule</term>
<term>Mater</term>
<term>Mccullough</term>
<term>Mccullough method</term>
<term>Meoh</term>
<term>Mmol</term>
<term>Molecular weights</term>
<term>Monomer</term>
<term>Nonsubstituted</term>
<term>Nonsubstituted polythiophenes</term>
<term>P3ats</term>
<term>Polym</term>
<term>Polymer</term>
<term>Polymerization</term>
<term>Polystyrene standards</term>
<term>Polythiophene</term>
<term>Polythiophenes</term>
<term>Quenched</term>
<term>Reaction mixture</term>
<term>Regioregular</term>
<term>Regioregular polythiophenes</term>
<term>Rieke</term>
<term>Soxhlet</term>
<term>Soxhlet extractions</term>
<term>Soxhlet thimble</term>
<term>Synth</term>
<term>Synthetic method</term>
<term>Synthetic methods</term>
<term>Synthetic procedures</term>
<term>Thiophene</term>
<term>Thiophene monomers</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Polymère</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract">Conjugated polymers have garnered a surplus of attention ever since the discovery of their promising and diverse electrical and optical properties. Thus, the term “organic electronics” has arisen due to the vast amount of interest in semiconductor polymeric materials. Of this conjugated polymers family, Polythiophenes and their derivatives remain one of the most highly researched in the “organic electronics” area. Their solubility, processability, high conductivity, low cost and ease of synthesis offer an attractive route towards modifiable semiconductors that can be tailored for specific applications. This chapter will delve into the history of polythiophenes with emphasis on polymerization techniques and synthetic experimental details.</div>
</front>
</TEI>
<affiliations><list><country><li>États-Unis</li>
</country>
<region><li>Pennsylvanie</li>
</region>
</list>
<tree><country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Haynes, Dahlia" sort="Haynes, Dahlia" uniqKey="Haynes D" first="Dahlia" last="Haynes">Dahlia Haynes</name>
</region>
<name sortKey="Haynes, Dahlia" sort="Haynes, Dahlia" uniqKey="Haynes D" first="Dahlia" last="Haynes">Dahlia Haynes</name>
<name sortKey="Haynes, Dahlia" sort="Haynes, Dahlia" uniqKey="Haynes D" first="Dahlia" last="Haynes">Dahlia Haynes</name>
<name sortKey="Mccullough, Richard" sort="Mccullough, Richard" uniqKey="Mccullough R" first="Richard" last="Mccullough">Richard Mccullough</name>
<name sortKey="Mccullough, Richard" sort="Mccullough, Richard" uniqKey="Mccullough R" first="Richard" last="Mccullough">Richard Mccullough</name>
<name sortKey="Mccullough, Richard" sort="Mccullough, Richard" uniqKey="Mccullough R" first="Richard" last="Mccullough">Richard Mccullough</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Amérique/explor/PittsburghV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004517 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 004517 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Amérique |area= PittsburghV1 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:84C4226EB7729DC751C30AC714D830E327E0913B |texte= CHAPTER 9 - Polythiophenes }}
This area was generated with Dilib version V0.6.38. |