Cargando…
Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media
Soluble model compounds, such as flavones, are frequently employed in initial and mechanistic studies under homogeneous conditions in the search for effective bleaching catalysts for raw cotton. The relevance of model substrates, such as morin and chrysin, and especially their reactivity with mangan...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474262/ https://www.ncbi.nlm.nih.gov/pubmed/31031566 http://dx.doi.org/10.1002/ejic.201800288 |
_version_ | 1783412604807413760 |
---|---|
author | Abdolahzadeh, Shaghayegh Boyle, Nicola M. Hage, Ronald de Boer, Johannes W. Browne, Wesley R. |
author_facet | Abdolahzadeh, Shaghayegh Boyle, Nicola M. Hage, Ronald de Boer, Johannes W. Browne, Wesley R. |
author_sort | Abdolahzadeh, Shaghayegh |
collection | PubMed |
description | Soluble model compounds, such as flavones, are frequently employed in initial and mechanistic studies under homogeneous conditions in the search for effective bleaching catalysts for raw cotton. The relevance of model substrates, such as morin and chrysin, and especially their reactivity with manganese catalysts [i.e. in combination with 1,4,7‐triazacyclononane (tacn) based ligands] applied in raw cotton bleaching with H(2)O(2) in alkaline solutions is examined. We show that morin, used frequently as a model, is highly sensitive to oxidation with O(2), by processes catalyzed by trace metal ions, that can be accelerated photochemically, although not involve generation of (1)O(2). The structurally related chrysin is not susceptible to such photo‐accelerated oxidation with O(2). Furthermore, chrysin is oxidized by H(2)O(2) only in the presence of a Mn‐tacn based catalyst, and does not undergo oxidation with O(2) as terminal oxidant. Chrysin mimics the behavior of raw cotton's chromophores in their catalyzed oxidation with H(2)O(2), and is likely a mechanistically relevant model compound for the study of transition metal catalysts for dye bleaching catalysts under homogeneous conditions. |
format | Online Article Text |
id | pubmed-6474262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64742622019-04-24 Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media Abdolahzadeh, Shaghayegh Boyle, Nicola M. Hage, Ronald de Boer, Johannes W. Browne, Wesley R. Eur J Inorg Chem Full Papers Soluble model compounds, such as flavones, are frequently employed in initial and mechanistic studies under homogeneous conditions in the search for effective bleaching catalysts for raw cotton. The relevance of model substrates, such as morin and chrysin, and especially their reactivity with manganese catalysts [i.e. in combination with 1,4,7‐triazacyclononane (tacn) based ligands] applied in raw cotton bleaching with H(2)O(2) in alkaline solutions is examined. We show that morin, used frequently as a model, is highly sensitive to oxidation with O(2), by processes catalyzed by trace metal ions, that can be accelerated photochemically, although not involve generation of (1)O(2). The structurally related chrysin is not susceptible to such photo‐accelerated oxidation with O(2). Furthermore, chrysin is oxidized by H(2)O(2) only in the presence of a Mn‐tacn based catalyst, and does not undergo oxidation with O(2) as terminal oxidant. Chrysin mimics the behavior of raw cotton's chromophores in their catalyzed oxidation with H(2)O(2), and is likely a mechanistically relevant model compound for the study of transition metal catalysts for dye bleaching catalysts under homogeneous conditions. John Wiley and Sons Inc. 2018-05-29 2018-06-22 /pmc/articles/PMC6474262/ /pubmed/31031566 http://dx.doi.org/10.1002/ejic.201800288 Text en © 2018 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-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 Abdolahzadeh, Shaghayegh Boyle, Nicola M. Hage, Ronald de Boer, Johannes W. Browne, Wesley R. Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media |
title | Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media |
title_full | Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media |
title_fullStr | Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media |
title_full_unstemmed | Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media |
title_short | Metal‐Catalyzed Photooxidation of Flavones in Aqueous Media |
title_sort | metal‐catalyzed photooxidation of flavones in aqueous media |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474262/ https://www.ncbi.nlm.nih.gov/pubmed/31031566 http://dx.doi.org/10.1002/ejic.201800288 |
work_keys_str_mv | AT abdolahzadehshaghayegh metalcatalyzedphotooxidationofflavonesinaqueousmedia AT boylenicolam metalcatalyzedphotooxidationofflavonesinaqueousmedia AT hageronald metalcatalyzedphotooxidationofflavonesinaqueousmedia AT deboerjohannesw metalcatalyzedphotooxidationofflavonesinaqueousmedia AT brownewesleyr metalcatalyzedphotooxidationofflavonesinaqueousmedia |