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Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols

An efficient one-pot synthesis for Janus-type fullerenol derivatives and how to characterize them is reported. This synthesis provides access to asymmetrically substituted fullerenol with five substituents on one pole of the fullerene and polyhydroxylation moieties, mostly ether and hydroxy groups,...

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Autores principales: Kunkel, Marius, Polarz, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466692/
https://www.ncbi.nlm.nih.gov/pubmed/31019582
http://dx.doi.org/10.3762/bjoc.15.87
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author Kunkel, Marius
Polarz, Sebastian
author_facet Kunkel, Marius
Polarz, Sebastian
author_sort Kunkel, Marius
collection PubMed
description An efficient one-pot synthesis for Janus-type fullerenol derivatives and how to characterize them is reported. This synthesis provides access to asymmetrically substituted fullerenol with five substituents on one pole of the fullerene and polyhydroxylation moieties, mostly ether and hydroxy groups, on the rest of the fullerene core. As substituents a broad variety of primary amines can be used to obtain Janus-type amphiphilic fullerenols in good to excellent yield. These fullerenol amphiphiles can serve as suitable precursors for further reactions resulting in new applications for fullerenols.
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spelling pubmed-64666922019-04-24 Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols Kunkel, Marius Polarz, Sebastian Beilstein J Org Chem Letter An efficient one-pot synthesis for Janus-type fullerenol derivatives and how to characterize them is reported. This synthesis provides access to asymmetrically substituted fullerenol with five substituents on one pole of the fullerene and polyhydroxylation moieties, mostly ether and hydroxy groups, on the rest of the fullerene core. As substituents a broad variety of primary amines can be used to obtain Janus-type amphiphilic fullerenols in good to excellent yield. These fullerenol amphiphiles can serve as suitable precursors for further reactions resulting in new applications for fullerenols. Beilstein-Institut 2019-04-12 /pmc/articles/PMC6466692/ /pubmed/31019582 http://dx.doi.org/10.3762/bjoc.15.87 Text en Copyright © 2019, Kunkel and Polarz https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Kunkel, Marius
Polarz, Sebastian
Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols
title Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols
title_full Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols
title_fullStr Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols
title_full_unstemmed Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols
title_short Easy, efficient and versatile one-pot synthesis of Janus-type-substituted fullerenols
title_sort easy, efficient and versatile one-pot synthesis of janus-type-substituted fullerenols
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466692/
https://www.ncbi.nlm.nih.gov/pubmed/31019582
http://dx.doi.org/10.3762/bjoc.15.87
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