Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa

A series of selenophene oligomers incorporating conjugated fluorinated phenylene units have been synthesised as potential semiconductor materials for organic field-effect transistors (OFETs). X-ray crystallography shows that the molecules are held in close proximity by several short intermolecular c...

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Detalles Bibliográficos
Autores principales: Crouch, David J, Skabara, Peter J, Heeney, Martin, McCulloch, Iain, Sparrowe, David, Coles, Simon J, Hursthouse, Michael B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2008
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810712/
http://dx.doi.org/10.1002/marc.200800449
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author Crouch, David J
Skabara, Peter J
Heeney, Martin
McCulloch, Iain
Sparrowe, David
Coles, Simon J
Hursthouse, Michael B
author_facet Crouch, David J
Skabara, Peter J
Heeney, Martin
McCulloch, Iain
Sparrowe, David
Coles, Simon J
Hursthouse, Michael B
author_sort Crouch, David J
collection PubMed
description A series of selenophene oligomers incorporating conjugated fluorinated phenylene units have been synthesised as potential semiconductor materials for organic field-effect transistors (OFETs). X-ray crystallography shows that the molecules are held in close proximity by several short intermolecular contacts, making them ideal candidates for OFET applications.
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spelling pubmed-38107122013-11-06 Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa Crouch, David J Skabara, Peter J Heeney, Martin McCulloch, Iain Sparrowe, David Coles, Simon J Hursthouse, Michael B Macromol Rapid Commun Communications A series of selenophene oligomers incorporating conjugated fluorinated phenylene units have been synthesised as potential semiconductor materials for organic field-effect transistors (OFETs). X-ray crystallography shows that the molecules are held in close proximity by several short intermolecular contacts, making them ideal candidates for OFET applications. WILEY-VCH Verlag 2008-11-19 2008-10-15 /pmc/articles/PMC3810712/ http://dx.doi.org/10.1002/marc.200800449 Text en Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Communications
Crouch, David J
Skabara, Peter J
Heeney, Martin
McCulloch, Iain
Sparrowe, David
Coles, Simon J
Hursthouse, Michael B
Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa
title Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa
title_full Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa
title_fullStr Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa
title_full_unstemmed Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa
title_short Hexyl-Substituted Oligoselenophenes with Central Tetrafluorophenylene Units: Synthesis, Characterisation and Application in Organic Field Effect Transistorsa
title_sort hexyl-substituted oligoselenophenes with central tetrafluorophenylene units: synthesis, characterisation and application in organic field effect transistorsa
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810712/
http://dx.doi.org/10.1002/marc.200800449
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