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Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination
Different types of high‐yield, easily scalable syntheses for cyano(fluoro)borates Kt[BF(n)(CN)(4−n)] (n=0–2) (Kt=cation), which are versatile building blocks for materials applications and chemical synthesis, have been developed. Tetrafluoroborates react with trimethylsilyl cyanide in the presence o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540003/ https://www.ncbi.nlm.nih.gov/pubmed/32453869 http://dx.doi.org/10.1002/chem.202002324 |
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author | Drisch, Michael Bischoff, Lisa A. Sprenger, Jan A. P. Hennig, Philipp T. Wirthensohn, Raphael Landmann, Johannes Konieczka, Szymon Z. Hailmann, Michael Ignat'ev, Nikolai V. Finze, Maik |
author_facet | Drisch, Michael Bischoff, Lisa A. Sprenger, Jan A. P. Hennig, Philipp T. Wirthensohn, Raphael Landmann, Johannes Konieczka, Szymon Z. Hailmann, Michael Ignat'ev, Nikolai V. Finze, Maik |
author_sort | Drisch, Michael |
collection | PubMed |
description | Different types of high‐yield, easily scalable syntheses for cyano(fluoro)borates Kt[BF(n)(CN)(4−n)] (n=0–2) (Kt=cation), which are versatile building blocks for materials applications and chemical synthesis, have been developed. Tetrafluoroborates react with trimethylsilyl cyanide in the presence of metal‐free Brønsted or Lewis acid catalysts under unprecedentedly mild conditions to give tricyanofluoroborates or tetracyanoborates. Analogously, pentafluoroethyltrifluoroborates are converted into pentafluoroethyltricyanoborates. Boron trifluoride etherate, alkali metal salts, and trimethylsilyl cyanide selectively yield dicyanodifluoroborates or tricyanofluoroborates. Fluorination of cyanohydridoborates is the third reaction type that includes direct fluorination with, for example, elemental fluorine, stepwise halogenation/fluorination reactions, and electrochemical fluorination (ECF) according to the Simons process. In addition, fluorination of [BH(CN)(2){OC(O)Et}](−) to result in [BF(CN)(2){OC(O)Et}](−) is described. |
format | Online Article Text |
id | pubmed-7540003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75400032020-10-09 Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination Drisch, Michael Bischoff, Lisa A. Sprenger, Jan A. P. Hennig, Philipp T. Wirthensohn, Raphael Landmann, Johannes Konieczka, Szymon Z. Hailmann, Michael Ignat'ev, Nikolai V. Finze, Maik Chemistry Full Papers Different types of high‐yield, easily scalable syntheses for cyano(fluoro)borates Kt[BF(n)(CN)(4−n)] (n=0–2) (Kt=cation), which are versatile building blocks for materials applications and chemical synthesis, have been developed. Tetrafluoroborates react with trimethylsilyl cyanide in the presence of metal‐free Brønsted or Lewis acid catalysts under unprecedentedly mild conditions to give tricyanofluoroborates or tetracyanoborates. Analogously, pentafluoroethyltrifluoroborates are converted into pentafluoroethyltricyanoborates. Boron trifluoride etherate, alkali metal salts, and trimethylsilyl cyanide selectively yield dicyanodifluoroborates or tricyanofluoroborates. Fluorination of cyanohydridoborates is the third reaction type that includes direct fluorination with, for example, elemental fluorine, stepwise halogenation/fluorination reactions, and electrochemical fluorination (ECF) according to the Simons process. In addition, fluorination of [BH(CN)(2){OC(O)Et}](−) to result in [BF(CN)(2){OC(O)Et}](−) is described. John Wiley and Sons Inc. 2020-08-04 2020-09-04 /pmc/articles/PMC7540003/ /pubmed/32453869 http://dx.doi.org/10.1002/chem.202002324 Text en © 2020 The Authors. Published by Wiley-VCH GmbH 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 | Full Papers Drisch, Michael Bischoff, Lisa A. Sprenger, Jan A. P. Hennig, Philipp T. Wirthensohn, Raphael Landmann, Johannes Konieczka, Szymon Z. Hailmann, Michael Ignat'ev, Nikolai V. Finze, Maik Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination |
title | Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination |
title_full | Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination |
title_fullStr | Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination |
title_full_unstemmed | Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination |
title_short | Innovative Syntheses of Cyano(fluoro)borates: Catalytic Cyanation, Electrochemical and Electrophilic Fluorination |
title_sort | innovative syntheses of cyano(fluoro)borates: catalytic cyanation, electrochemical and electrophilic fluorination |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540003/ https://www.ncbi.nlm.nih.gov/pubmed/32453869 http://dx.doi.org/10.1002/chem.202002324 |
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