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Hydrodechlorination of Aryl Chlorides Under Biocompatible Conditions
[Image: see text] Developing nonenzymatic chemistry that is nontoxic to microbial organisms creates the potential to integrate synthetic chemistry with metabolism and offers new remediation strategies. Chlorinated organic compounds known to bioaccumulate and cause harmful environmental impact can be...
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/PMC9097202/ https://www.ncbi.nlm.nih.gov/pubmed/35571846 http://dx.doi.org/10.1021/acsomega.2c01204 |
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author | Gomez, Karen P. Clay-Barbour, Emma Schiet, Giselle Z. Stubbs, Samantha AbuBakar, Mohammed Shanker, Rhyan B. Schultz, Erica E. |
author_facet | Gomez, Karen P. Clay-Barbour, Emma Schiet, Giselle Z. Stubbs, Samantha AbuBakar, Mohammed Shanker, Rhyan B. Schultz, Erica E. |
author_sort | Gomez, Karen P. |
collection | PubMed |
description | [Image: see text] Developing nonenzymatic chemistry that is nontoxic to microbial organisms creates the potential to integrate synthetic chemistry with metabolism and offers new remediation strategies. Chlorinated organic compounds known to bioaccumulate and cause harmful environmental impact can be converted into less damaging derivatives through hydrodehalogenation. The hydrodechlorination of substituted aryl chlorides using Pd/C and ammonium formate in biological media under physiological conditions (neutral pH, moderate temperature, and ambient pressure) is reported. The reaction conditions were successful for a range of aryl chlorides with electron-donating and -withdrawing groups, limited by the solubility of substrates in aqueous media. Soluble substrates gave good yields (60–98%) of the reduction product within 48 h. The relative toxicities of each reaction component were tested separately and together against bacteria, and the reaction proceeded in bacterial cultures containing an aryl chloride with robust cell growth. This work offers an initial step toward the removal of aryl chlorides from waste streams that currently use bacterial degradation to remove pollutants. |
format | Online Article Text |
id | pubmed-9097202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90972022022-05-13 Hydrodechlorination of Aryl Chlorides Under Biocompatible Conditions Gomez, Karen P. Clay-Barbour, Emma Schiet, Giselle Z. Stubbs, Samantha AbuBakar, Mohammed Shanker, Rhyan B. Schultz, Erica E. ACS Omega [Image: see text] Developing nonenzymatic chemistry that is nontoxic to microbial organisms creates the potential to integrate synthetic chemistry with metabolism and offers new remediation strategies. Chlorinated organic compounds known to bioaccumulate and cause harmful environmental impact can be converted into less damaging derivatives through hydrodehalogenation. The hydrodechlorination of substituted aryl chlorides using Pd/C and ammonium formate in biological media under physiological conditions (neutral pH, moderate temperature, and ambient pressure) is reported. The reaction conditions were successful for a range of aryl chlorides with electron-donating and -withdrawing groups, limited by the solubility of substrates in aqueous media. Soluble substrates gave good yields (60–98%) of the reduction product within 48 h. The relative toxicities of each reaction component were tested separately and together against bacteria, and the reaction proceeded in bacterial cultures containing an aryl chloride with robust cell growth. This work offers an initial step toward the removal of aryl chlorides from waste streams that currently use bacterial degradation to remove pollutants. American Chemical Society 2022-04-25 /pmc/articles/PMC9097202/ /pubmed/35571846 http://dx.doi.org/10.1021/acsomega.2c01204 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Gomez, Karen P. Clay-Barbour, Emma Schiet, Giselle Z. Stubbs, Samantha AbuBakar, Mohammed Shanker, Rhyan B. Schultz, Erica E. Hydrodechlorination of Aryl Chlorides Under Biocompatible Conditions |
title | Hydrodechlorination of Aryl Chlorides Under Biocompatible
Conditions |
title_full | Hydrodechlorination of Aryl Chlorides Under Biocompatible
Conditions |
title_fullStr | Hydrodechlorination of Aryl Chlorides Under Biocompatible
Conditions |
title_full_unstemmed | Hydrodechlorination of Aryl Chlorides Under Biocompatible
Conditions |
title_short | Hydrodechlorination of Aryl Chlorides Under Biocompatible
Conditions |
title_sort | hydrodechlorination of aryl chlorides under biocompatible
conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097202/ https://www.ncbi.nlm.nih.gov/pubmed/35571846 http://dx.doi.org/10.1021/acsomega.2c01204 |
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