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Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers

The implementation of nano/microelectronic devices requires efficient strategies for the realization of supramolecular structures with desired function and supported on appropriate substrates. This article illustrates a strategy based on the synthesis of thiophene oligomers having the same “sulfur‐o...

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Detalles Bibliográficos
Autores principales: Zangoli, Mattia, Di Maria, Francesca, Barbarella, Giovanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175019/
https://www.ncbi.nlm.nih.gov/pubmed/32328405
http://dx.doi.org/10.1002/open.201900347
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author Zangoli, Mattia
Di Maria, Francesca
Barbarella, Giovanna
author_facet Zangoli, Mattia
Di Maria, Francesca
Barbarella, Giovanna
author_sort Zangoli, Mattia
collection PubMed
description The implementation of nano/microelectronic devices requires efficient strategies for the realization of supramolecular structures with desired function and supported on appropriate substrates. This article illustrates a strategy based on the synthesis of thiophene oligomers having the same “sulfur‐overrich” quaterthiophene inner core (non bonding interactional algorithm) and different terminal groups. Nano/microfibers are formed on surfaces having a morphology independent of the nature of the deposition substrate and displaying a wide tuning of properties that make the fibers optoelectronically suitable for application in devices.
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spelling pubmed-71750192020-04-23 Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers Zangoli, Mattia Di Maria, Francesca Barbarella, Giovanna ChemistryOpen Minireviews The implementation of nano/microelectronic devices requires efficient strategies for the realization of supramolecular structures with desired function and supported on appropriate substrates. This article illustrates a strategy based on the synthesis of thiophene oligomers having the same “sulfur‐overrich” quaterthiophene inner core (non bonding interactional algorithm) and different terminal groups. Nano/microfibers are formed on surfaces having a morphology independent of the nature of the deposition substrate and displaying a wide tuning of properties that make the fibers optoelectronically suitable for application in devices. John Wiley and Sons Inc. 2020-04-22 /pmc/articles/PMC7175019/ /pubmed/32328405 http://dx.doi.org/10.1002/open.201900347 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Minireviews
Zangoli, Mattia
Di Maria, Francesca
Barbarella, Giovanna
Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers
title Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers
title_full Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers
title_fullStr Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers
title_full_unstemmed Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers
title_short Supramolecular Assembly of Thiophene‐Based Oligomers into Nanostructured Fluorescent Conductive and Chiral Microfibers
title_sort supramolecular assembly of thiophene‐based oligomers into nanostructured fluorescent conductive and chiral microfibers
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175019/
https://www.ncbi.nlm.nih.gov/pubmed/32328405
http://dx.doi.org/10.1002/open.201900347
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