Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sheberla, Dennis, Patra, Snehangshu, Wijsboom, Yair H., Sharma, Sagar, Sheynin, Yana, Haj-Yahia, Abd-Elrazek, Barak, Adva Hayoun, Gidron, Ori, Bendikov, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
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
_version_ 1783261770297638912
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
title_full Conducting polyfurans by electropolymerization of oligofurans
title_fullStr Conducting polyfurans by electropolymerization of oligofurans
title_full_unstemmed Conducting polyfurans by electropolymerization of oligofurans
title_short Conducting polyfurans by electropolymerization of oligofurans
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
work_keys_str_mv AT sheberladennis conductingpolyfuransbyelectropolymerizationofoligofurans
AT patrasnehangshu conductingpolyfuransbyelectropolymerizationofoligofurans
AT wijsboomyairh conductingpolyfuransbyelectropolymerizationofoligofurans
AT sharmasagar conductingpolyfuransbyelectropolymerizationofoligofurans
AT sheyninyana conductingpolyfuransbyelectropolymerizationofoligofurans
AT hajyahiaabdelrazek conductingpolyfuransbyelectropolymerizationofoligofurans
AT barakadvahayoun conductingpolyfuransbyelectropolymerizationofoligofurans
AT gidronori conductingpolyfuransbyelectropolymerizationofoligofurans
AT bendikovmichael conductingpolyfuransbyelectropolymerizationofoligofurans