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Toward Environmentally Benign Electrophilic Chlorinations: From Chloroperoxidase to Bioinspired Isoporphyrins
[Image: see text] Recent desires to develop environmentally benign procedures for electrophilic chlorinations have encouraged researchers to take inspiration from nature. In particular, the enzyme chloroperoxidase (CPO), which is capable of electrophilic chlorinations through the umpolung of chlorid...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157495/ https://www.ncbi.nlm.nih.gov/pubmed/35574587 http://dx.doi.org/10.1021/acs.inorgchem.2c00602 |
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author | Engbers, Silène Hage, Ronald Klein, Johannes E. M. N. |
author_facet | Engbers, Silène Hage, Ronald Klein, Johannes E. M. N. |
author_sort | Engbers, Silène |
collection | PubMed |
description | [Image: see text] Recent desires to develop environmentally benign procedures for electrophilic chlorinations have encouraged researchers to take inspiration from nature. In particular, the enzyme chloroperoxidase (CPO), which is capable of electrophilic chlorinations through the umpolung of chloride by oxidation with hydrogen peroxide (H(2)O(2)), has received lots of attention. CPO itself is unsuitable for industrial use because of its tendency to decompose in the presence of excess H(2)O(2). Biomimetic complexes (CPO active-site mimics) were then developed and have been shown to successfully catalyze electrophilic chlorinations but are too synthetically demanding to be economically viable. Reported efforts at generating the putative active chlorinating agent of CPO (an iron hypochlorite species) via the umpolung of chloride and using simple meso-substituted iron porphyrins were unsuccessful. Instead, a meso-chloroisoporphyrin intermediate was formed, which was shown to be equally capable of performing electrophilic chlorinations. The current developments toward a potential method involving this novel intermediate for environmentally benign electrophilic chlorinations are discussed. Although this novel pathway no longer follows the mechanism of CPO, it was developed from efforts to replicate its function, showing the power that drawing inspiration from nature can have. |
format | Online Article Text |
id | pubmed-9157495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91574952022-06-02 Toward Environmentally Benign Electrophilic Chlorinations: From Chloroperoxidase to Bioinspired Isoporphyrins Engbers, Silène Hage, Ronald Klein, Johannes E. M. N. Inorg Chem [Image: see text] Recent desires to develop environmentally benign procedures for electrophilic chlorinations have encouraged researchers to take inspiration from nature. In particular, the enzyme chloroperoxidase (CPO), which is capable of electrophilic chlorinations through the umpolung of chloride by oxidation with hydrogen peroxide (H(2)O(2)), has received lots of attention. CPO itself is unsuitable for industrial use because of its tendency to decompose in the presence of excess H(2)O(2). Biomimetic complexes (CPO active-site mimics) were then developed and have been shown to successfully catalyze electrophilic chlorinations but are too synthetically demanding to be economically viable. Reported efforts at generating the putative active chlorinating agent of CPO (an iron hypochlorite species) via the umpolung of chloride and using simple meso-substituted iron porphyrins were unsuccessful. Instead, a meso-chloroisoporphyrin intermediate was formed, which was shown to be equally capable of performing electrophilic chlorinations. The current developments toward a potential method involving this novel intermediate for environmentally benign electrophilic chlorinations are discussed. Although this novel pathway no longer follows the mechanism of CPO, it was developed from efforts to replicate its function, showing the power that drawing inspiration from nature can have. American Chemical Society 2022-05-15 2022-05-30 /pmc/articles/PMC9157495/ /pubmed/35574587 http://dx.doi.org/10.1021/acs.inorgchem.2c00602 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Engbers, Silène Hage, Ronald Klein, Johannes E. M. N. Toward Environmentally Benign Electrophilic Chlorinations: From Chloroperoxidase to Bioinspired Isoporphyrins |
title | Toward Environmentally Benign Electrophilic Chlorinations:
From Chloroperoxidase to Bioinspired Isoporphyrins |
title_full | Toward Environmentally Benign Electrophilic Chlorinations:
From Chloroperoxidase to Bioinspired Isoporphyrins |
title_fullStr | Toward Environmentally Benign Electrophilic Chlorinations:
From Chloroperoxidase to Bioinspired Isoporphyrins |
title_full_unstemmed | Toward Environmentally Benign Electrophilic Chlorinations:
From Chloroperoxidase to Bioinspired Isoporphyrins |
title_short | Toward Environmentally Benign Electrophilic Chlorinations:
From Chloroperoxidase to Bioinspired Isoporphyrins |
title_sort | toward environmentally benign electrophilic chlorinations:
from chloroperoxidase to bioinspired isoporphyrins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157495/ https://www.ncbi.nlm.nih.gov/pubmed/35574587 http://dx.doi.org/10.1021/acs.inorgchem.2c00602 |
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