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A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex
Through a rapid screening of Cp*Ir complexes based on a turn‐on type fluorescence readout, a [Cp*Ir(dipyrido[3,2‐a : 2’,3’‐c]phenazine)Cl](+) complex was found to catalyze the blue‐light promoted dehydrogenation of N‐heterocycles under physiological conditions. In the dehydrogenation of tetrahydrois...
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/PMC7984327/ https://www.ncbi.nlm.nih.gov/pubmed/33777249 http://dx.doi.org/10.1002/cctc.202000488 |
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author | Davis, Holly Jane Häussinger, Daniel Ward, Thomas R. Okamoto, Yasunori |
author_facet | Davis, Holly Jane Häussinger, Daniel Ward, Thomas R. Okamoto, Yasunori |
author_sort | Davis, Holly Jane |
collection | PubMed |
description | Through a rapid screening of Cp*Ir complexes based on a turn‐on type fluorescence readout, a [Cp*Ir(dipyrido[3,2‐a : 2’,3’‐c]phenazine)Cl](+) complex was found to catalyze the blue‐light promoted dehydrogenation of N‐heterocycles under physiological conditions. In the dehydrogenation of tetrahydroisoquinolines, the catalyst preferentially yielded the monodehydrogenated product, accompanying H(2)O(2) generation. We surmise that this mechanism may be reminiscent of flavin‐dependent oxidases. |
format | Online Article Text |
id | pubmed-7984327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79843272021-03-24 A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex Davis, Holly Jane Häussinger, Daniel Ward, Thomas R. Okamoto, Yasunori ChemCatChem Communications Through a rapid screening of Cp*Ir complexes based on a turn‐on type fluorescence readout, a [Cp*Ir(dipyrido[3,2‐a : 2’,3’‐c]phenazine)Cl](+) complex was found to catalyze the blue‐light promoted dehydrogenation of N‐heterocycles under physiological conditions. In the dehydrogenation of tetrahydroisoquinolines, the catalyst preferentially yielded the monodehydrogenated product, accompanying H(2)O(2) generation. We surmise that this mechanism may be reminiscent of flavin‐dependent oxidases. John Wiley and Sons Inc. 2020-07-22 2020-09-17 /pmc/articles/PMC7984327/ /pubmed/33777249 http://dx.doi.org/10.1002/cctc.202000488 Text en © 2020 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 Davis, Holly Jane Häussinger, Daniel Ward, Thomas R. Okamoto, Yasunori A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex |
title | A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex |
title_full | A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex |
title_fullStr | A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex |
title_full_unstemmed | A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex |
title_short | A Visible‐Light Promoted Amine Oxidation Catalyzed by a Cp*Ir Complex |
title_sort | visible‐light promoted amine oxidation catalyzed by a cp*ir complex |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984327/ https://www.ncbi.nlm.nih.gov/pubmed/33777249 http://dx.doi.org/10.1002/cctc.202000488 |
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