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Functional Graphene by Thiol‐ene Click Chemistry

Thiol‐ene click reaction was successfully employed for chemical modification of graphene oxide (GO) by one‐step synthesis. Herein, 2,2‐azobis(2‐methylpropionitrile) (AIBN) was used as thermal catalyst and cysteamine hydrochloride (HS−(CH(2))(2)−NH(2)HCl) was used as thiol‐containing compound, which...

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Autores principales: Luong, Nguyen Dang, Sinh, Le Hoang, Johansson, Leena‐Sisko, Campell, Joseph, Seppälä, Jukka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174942/
https://www.ncbi.nlm.nih.gov/pubmed/25580698
http://dx.doi.org/10.1002/chem.201405734
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author Luong, Nguyen Dang
Sinh, Le Hoang
Johansson, Leena‐Sisko
Campell, Joseph
Seppälä, Jukka
author_facet Luong, Nguyen Dang
Sinh, Le Hoang
Johansson, Leena‐Sisko
Campell, Joseph
Seppälä, Jukka
author_sort Luong, Nguyen Dang
collection PubMed
description Thiol‐ene click reaction was successfully employed for chemical modification of graphene oxide (GO) by one‐step synthesis. Herein, 2,2‐azobis(2‐methylpropionitrile) (AIBN) was used as thermal catalyst and cysteamine hydrochloride (HS−(CH(2))(2)−NH(2)HCl) was used as thiol‐containing compound, which is incorporated to GO surface upon reaction with the C=C bonds. The hydrochloride acts as protecting group for the amine, which is finally eliminated by adding sodium hydroxide. The modified GO contains both S‐ and N‐containing groups (NS‐GO). We found that NS‐GO sheets form good dispersion in water, ethanol, and ethylene glycol. These graphene dispersions can be processed into functionalized graphene film. Besides, it was demonstrated that NS‐GO was proved to be an excellent host matrix for platinum nanoparticles. The developed method paves a new way for graphene modification and its functional nanocomposites.
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spelling pubmed-61749422018-10-15 Functional Graphene by Thiol‐ene Click Chemistry Luong, Nguyen Dang Sinh, Le Hoang Johansson, Leena‐Sisko Campell, Joseph Seppälä, Jukka Chemistry Communications Thiol‐ene click reaction was successfully employed for chemical modification of graphene oxide (GO) by one‐step synthesis. Herein, 2,2‐azobis(2‐methylpropionitrile) (AIBN) was used as thermal catalyst and cysteamine hydrochloride (HS−(CH(2))(2)−NH(2)HCl) was used as thiol‐containing compound, which is incorporated to GO surface upon reaction with the C=C bonds. The hydrochloride acts as protecting group for the amine, which is finally eliminated by adding sodium hydroxide. The modified GO contains both S‐ and N‐containing groups (NS‐GO). We found that NS‐GO sheets form good dispersion in water, ethanol, and ethylene glycol. These graphene dispersions can be processed into functionalized graphene film. Besides, it was demonstrated that NS‐GO was proved to be an excellent host matrix for platinum nanoparticles. The developed method paves a new way for graphene modification and its functional nanocomposites. John Wiley and Sons Inc. 2015-01-07 2015-02-16 /pmc/articles/PMC6174942/ /pubmed/25580698 http://dx.doi.org/10.1002/chem.201405734 Text en © 20115 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Luong, Nguyen Dang
Sinh, Le Hoang
Johansson, Leena‐Sisko
Campell, Joseph
Seppälä, Jukka
Functional Graphene by Thiol‐ene Click Chemistry
title Functional Graphene by Thiol‐ene Click Chemistry
title_full Functional Graphene by Thiol‐ene Click Chemistry
title_fullStr Functional Graphene by Thiol‐ene Click Chemistry
title_full_unstemmed Functional Graphene by Thiol‐ene Click Chemistry
title_short Functional Graphene by Thiol‐ene Click Chemistry
title_sort functional graphene by thiol‐ene click chemistry
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174942/
https://www.ncbi.nlm.nih.gov/pubmed/25580698
http://dx.doi.org/10.1002/chem.201405734
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