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A Facile Route to C2-Substituted Imidazolium Ionic Liquids
A convenient route for the preparation of C2-substituted imidazolium ionic liquids is reported. This method involves the alkylation of N-heterocyclic carbenes, which are readily generated from the C2-unsubstituted imidazolium ionic liquids. It works well for non-functionalized alkyl chlorides, and l...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254211/ https://www.ncbi.nlm.nih.gov/pubmed/19553895 http://dx.doi.org/10.3390/molecules14062235 |
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author | Ennis, Elliot Handy, Scott T. |
author_facet | Ennis, Elliot Handy, Scott T. |
author_sort | Ennis, Elliot |
collection | PubMed |
description | A convenient route for the preparation of C2-substituted imidazolium ionic liquids is reported. This method involves the alkylation of N-heterocyclic carbenes, which are readily generated from the C2-unsubstituted imidazolium ionic liquids. It works well for non-functionalized alkyl chlorides, and less well for alkyl bromides and iodides, likely due to competing elimination reactions. The resulting C2-substituted salts can be transformed into ionic liquids via standard anion metathesis reactions. |
format | Online Article Text |
id | pubmed-6254211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62542112018-11-30 A Facile Route to C2-Substituted Imidazolium Ionic Liquids Ennis, Elliot Handy, Scott T. Molecules Article A convenient route for the preparation of C2-substituted imidazolium ionic liquids is reported. This method involves the alkylation of N-heterocyclic carbenes, which are readily generated from the C2-unsubstituted imidazolium ionic liquids. It works well for non-functionalized alkyl chlorides, and less well for alkyl bromides and iodides, likely due to competing elimination reactions. The resulting C2-substituted salts can be transformed into ionic liquids via standard anion metathesis reactions. Molecular Diversity Preservation International 2009-06-19 /pmc/articles/PMC6254211/ /pubmed/19553895 http://dx.doi.org/10.3390/molecules14062235 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Ennis, Elliot Handy, Scott T. A Facile Route to C2-Substituted Imidazolium Ionic Liquids |
title | A Facile Route to C2-Substituted Imidazolium Ionic Liquids |
title_full | A Facile Route to C2-Substituted Imidazolium Ionic Liquids |
title_fullStr | A Facile Route to C2-Substituted Imidazolium Ionic Liquids |
title_full_unstemmed | A Facile Route to C2-Substituted Imidazolium Ionic Liquids |
title_short | A Facile Route to C2-Substituted Imidazolium Ionic Liquids |
title_sort | facile route to c2-substituted imidazolium ionic liquids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254211/ https://www.ncbi.nlm.nih.gov/pubmed/19553895 http://dx.doi.org/10.3390/molecules14062235 |
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