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Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles
Selective in situ methylation of terminal chalcogenide ligands of molecular chalcogenido metalate anions in ionothermal reactions with alkylimidazolium-based ionic liquids yields a series of organo-functionalized chalcogenido metalate compounds. We present the syntheses and crystal structures of (C(...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540918/ https://www.ncbi.nlm.nih.gov/pubmed/31191876 http://dx.doi.org/10.1039/c9sc01358j |
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author | Peters, Bertram Santner, Silke Donsbach, Carsten Vöpel, Pascal Smarsly, Bernd Dehnen, Stefanie |
author_facet | Peters, Bertram Santner, Silke Donsbach, Carsten Vöpel, Pascal Smarsly, Bernd Dehnen, Stefanie |
author_sort | Peters, Bertram |
collection | PubMed |
description | Selective in situ methylation of terminal chalcogenide ligands of molecular chalcogenido metalate anions in ionothermal reactions with alkylimidazolium-based ionic liquids yields a series of organo-functionalized chalcogenido metalate compounds. We present the syntheses and crystal structures of (C(4)C(1)C(1)Im)(4+x)[Sn(10)S(16)O(4)(SMe)(4)][An](x) (1a–1f), (dmmpH)(6)[Mn(4)Sn(4)Se(13)(SeMe)(4)] (2), and (C(n)C(1)Im)(6)[Hg(6)Te(10)(TeMe)(2)] (3a, 3b). The methylation was confirmed by Raman spectroscopy, and the optical absorption properties of the methylated compounds were determined and compared to purely inorganic analogs. |
format | Online Article Text |
id | pubmed-6540918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-65409182019-06-12 Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles Peters, Bertram Santner, Silke Donsbach, Carsten Vöpel, Pascal Smarsly, Bernd Dehnen, Stefanie Chem Sci Chemistry Selective in situ methylation of terminal chalcogenide ligands of molecular chalcogenido metalate anions in ionothermal reactions with alkylimidazolium-based ionic liquids yields a series of organo-functionalized chalcogenido metalate compounds. We present the syntheses and crystal structures of (C(4)C(1)C(1)Im)(4+x)[Sn(10)S(16)O(4)(SMe)(4)][An](x) (1a–1f), (dmmpH)(6)[Mn(4)Sn(4)Se(13)(SeMe)(4)] (2), and (C(n)C(1)Im)(6)[Hg(6)Te(10)(TeMe)(2)] (3a, 3b). The methylation was confirmed by Raman spectroscopy, and the optical absorption properties of the methylated compounds were determined and compared to purely inorganic analogs. Royal Society of Chemistry 2019-04-22 /pmc/articles/PMC6540918/ /pubmed/31191876 http://dx.doi.org/10.1039/c9sc01358j Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Peters, Bertram Santner, Silke Donsbach, Carsten Vöpel, Pascal Smarsly, Bernd Dehnen, Stefanie Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles |
title | Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles
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title_full | Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles
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title_fullStr | Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles
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title_full_unstemmed | Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles
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title_short | Ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles
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title_sort | ionic liquid cations as methylation agent for extremely weak chalcogenido metalate nucleophiles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540918/ https://www.ncbi.nlm.nih.gov/pubmed/31191876 http://dx.doi.org/10.1039/c9sc01358j |
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