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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...

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Autores principales: Gomez, Karen P., Clay-Barbour, Emma, Schiet, Giselle Z., Stubbs, Samantha, AbuBakar, Mohammed, Shanker, Rhyan B., Schultz, Erica E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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