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Interfacial Oxidative Oligomerization of Catechol
[Image: see text] The heterogeneous reaction between thin films of catechol exposed to O(3)(g) creates hydroxyl radicals (HO(•)) in situ, which in turn generate semiquinone radical intermediates in the path to form heavier polyhydroxylated biphenyl, terphenyl, and triphenylene products. Herein, the...
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/PMC9558612/ https://www.ncbi.nlm.nih.gov/pubmed/36249361 http://dx.doi.org/10.1021/acsomega.2c05290 |
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author | Guzman, Marcelo I. Pillar-Little, Elizabeth A. Eugene, Alexis J. |
author_facet | Guzman, Marcelo I. Pillar-Little, Elizabeth A. Eugene, Alexis J. |
author_sort | Guzman, Marcelo I. |
collection | PubMed |
description | [Image: see text] The heterogeneous reaction between thin films of catechol exposed to O(3)(g) creates hydroxyl radicals (HO(•)) in situ, which in turn generate semiquinone radical intermediates in the path to form heavier polyhydroxylated biphenyl, terphenyl, and triphenylene products. Herein, the alteration of catechol aromatic surfaces and their chemical composition are studied during the heterogeneous oxidation of catechol films by O(3)(g) molar ratios ≥ 230 ppbv at variable relative humidity levels (0% ≤ RH ≤ 90%). Fourier transform infrared micro-spectroscopy, atomic force microscopy, electrospray ionization mass spectrometry, and reverse-phase liquid chromatography with UV–visible and mass spectrometry detection provide new physical insights into understanding the surface reaction. A Langmuir–Hinshelwood mechanism is accounted to report reaction rates, half-lives, and reactive uptake coefficients for the system under variable relative humidity levels. The reactions reported explain how the oligomerization of polyphenols proceeds at interfaces to contribute to the formation of brown organic carbon in atmospheric aerosols. |
format | Online Article Text |
id | pubmed-9558612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95586122022-10-14 Interfacial Oxidative Oligomerization of Catechol Guzman, Marcelo I. Pillar-Little, Elizabeth A. Eugene, Alexis J. ACS Omega [Image: see text] The heterogeneous reaction between thin films of catechol exposed to O(3)(g) creates hydroxyl radicals (HO(•)) in situ, which in turn generate semiquinone radical intermediates in the path to form heavier polyhydroxylated biphenyl, terphenyl, and triphenylene products. Herein, the alteration of catechol aromatic surfaces and their chemical composition are studied during the heterogeneous oxidation of catechol films by O(3)(g) molar ratios ≥ 230 ppbv at variable relative humidity levels (0% ≤ RH ≤ 90%). Fourier transform infrared micro-spectroscopy, atomic force microscopy, electrospray ionization mass spectrometry, and reverse-phase liquid chromatography with UV–visible and mass spectrometry detection provide new physical insights into understanding the surface reaction. A Langmuir–Hinshelwood mechanism is accounted to report reaction rates, half-lives, and reactive uptake coefficients for the system under variable relative humidity levels. The reactions reported explain how the oligomerization of polyphenols proceeds at interfaces to contribute to the formation of brown organic carbon in atmospheric aerosols. American Chemical Society 2022-09-22 /pmc/articles/PMC9558612/ /pubmed/36249361 http://dx.doi.org/10.1021/acsomega.2c05290 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 | Guzman, Marcelo I. Pillar-Little, Elizabeth A. Eugene, Alexis J. Interfacial Oxidative Oligomerization of Catechol |
title | Interfacial Oxidative
Oligomerization of Catechol |
title_full | Interfacial Oxidative
Oligomerization of Catechol |
title_fullStr | Interfacial Oxidative
Oligomerization of Catechol |
title_full_unstemmed | Interfacial Oxidative
Oligomerization of Catechol |
title_short | Interfacial Oxidative
Oligomerization of Catechol |
title_sort | interfacial oxidative
oligomerization of catechol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558612/ https://www.ncbi.nlm.nih.gov/pubmed/36249361 http://dx.doi.org/10.1021/acsomega.2c05290 |
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