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Conducting polyfurans by electropolymerization of oligofurans
Polyfurans have never been established as useful conjugated polymers, as previously they were considered to be inherently unstable and poorly conductive. Here, we show the preparation of stable and conducting polyfuran films by electropolymerization of a series of oligofurans of different chain leng...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586207/ https://www.ncbi.nlm.nih.gov/pubmed/28966762 http://dx.doi.org/10.1039/c4sc02664k |
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author | Sheberla, Dennis Patra, Snehangshu Wijsboom, Yair H. Sharma, Sagar Sheynin, Yana Haj-Yahia, Abd-Elrazek Barak, Adva Hayoun Gidron, Ori Bendikov, Michael |
author_facet | Sheberla, Dennis Patra, Snehangshu Wijsboom, Yair H. Sharma, Sagar Sheynin, Yana Haj-Yahia, Abd-Elrazek Barak, Adva Hayoun Gidron, Ori Bendikov, Michael |
author_sort | Sheberla, Dennis |
collection | PubMed |
description | Polyfurans have never been established as useful conjugated polymers, as previously they were considered to be inherently unstable and poorly conductive. Here, we show the preparation of stable and conducting polyfuran films by electropolymerization of a series of oligofurans of different chain lengths substituted with alkyl groups. The polyfuran films show good conductivity in the order of 1 S cm(–1), good environmental and electrochemical stabilities, very smooth morphologies (roughness 1–5 nm), long effective conjugation lengths, well-defined spectroelectrochemistry and electro-optical switching (in the Vis-NIR region), and have optical band-gaps in the range of 2.2–2.3 eV. A low oxidation potential needed for polymerization of oligofurans (compared to furan) is a key factor in achievement of improved properties of polyfurans reported in this work. DFT calculations and experiments show that polyfurans are much more rigid than polythiophenes, and alkyl substitution does not disturb backbone planarity and conjugation. The obtained properties of polyfuran films are similar or superior to the properties of electrochemically prepared poly(oligothiophene)s under similar conditions. |
format | Online Article Text |
id | pubmed-5586207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-55862072017-09-29 Conducting polyfurans by electropolymerization of oligofurans Sheberla, Dennis Patra, Snehangshu Wijsboom, Yair H. Sharma, Sagar Sheynin, Yana Haj-Yahia, Abd-Elrazek Barak, Adva Hayoun Gidron, Ori Bendikov, Michael Chem Sci Chemistry Polyfurans have never been established as useful conjugated polymers, as previously they were considered to be inherently unstable and poorly conductive. Here, we show the preparation of stable and conducting polyfuran films by electropolymerization of a series of oligofurans of different chain lengths substituted with alkyl groups. The polyfuran films show good conductivity in the order of 1 S cm(–1), good environmental and electrochemical stabilities, very smooth morphologies (roughness 1–5 nm), long effective conjugation lengths, well-defined spectroelectrochemistry and electro-optical switching (in the Vis-NIR region), and have optical band-gaps in the range of 2.2–2.3 eV. A low oxidation potential needed for polymerization of oligofurans (compared to furan) is a key factor in achievement of improved properties of polyfurans reported in this work. DFT calculations and experiments show that polyfurans are much more rigid than polythiophenes, and alkyl substitution does not disturb backbone planarity and conjugation. The obtained properties of polyfuran films are similar or superior to the properties of electrochemically prepared poly(oligothiophene)s under similar conditions. Royal Society of Chemistry 2015-01-01 2014-10-17 /pmc/articles/PMC5586207/ /pubmed/28966762 http://dx.doi.org/10.1039/c4sc02664k Text en This journal is © The Royal Society of Chemistry 2014 https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Sheberla, Dennis Patra, Snehangshu Wijsboom, Yair H. Sharma, Sagar Sheynin, Yana Haj-Yahia, Abd-Elrazek Barak, Adva Hayoun Gidron, Ori Bendikov, Michael Conducting polyfurans by electropolymerization of oligofurans |
title | Conducting polyfurans by electropolymerization of oligofurans
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title_full | Conducting polyfurans by electropolymerization of oligofurans
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title_fullStr | Conducting polyfurans by electropolymerization of oligofurans
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title_full_unstemmed | Conducting polyfurans by electropolymerization of oligofurans
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title_short | Conducting polyfurans by electropolymerization of oligofurans
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title_sort | conducting polyfurans by electropolymerization of oligofurans |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586207/ https://www.ncbi.nlm.nih.gov/pubmed/28966762 http://dx.doi.org/10.1039/c4sc02664k |
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