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A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect
Natural and anthropogenic activities result in the production of polycyclic aromatic hydrocarbons (PAHs), persistent pollutants that negatively impact the environment and human health. Rapid and reliable methods for the detection and discrimination of these compounds remains a technological challeng...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020785/ https://www.ncbi.nlm.nih.gov/pubmed/32110311 http://dx.doi.org/10.1039/c9sc03405f |
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author | Tropp, Joshua Ihde, Michael H. Williams, Abagail K. White, Nicholas J. Eedugurala, Naresh Bell, Noel C. Azoulay, Jason D. Bonizzoni, Marco |
author_facet | Tropp, Joshua Ihde, Michael H. Williams, Abagail K. White, Nicholas J. Eedugurala, Naresh Bell, Noel C. Azoulay, Jason D. Bonizzoni, Marco |
author_sort | Tropp, Joshua |
collection | PubMed |
description | Natural and anthropogenic activities result in the production of polycyclic aromatic hydrocarbons (PAHs), persistent pollutants that negatively impact the environment and human health. Rapid and reliable methods for the detection and discrimination of these compounds remains a technological challenge owing to their relatively featureless properties, structural similarities, and existence as complex mixtures. Here, we demonstrate that the inner filter effect (IFE), in combination with conjugated polymer (CP) array-based sensing, offers a straightforward approach for the quantitative and qualitative profiling of PAHs. The sensor array was constructed from six fluorescent fluorene-based copolymers, which incorporate side chains with peripheral 2-phenylbenzimidazole substituents that provide spectral overlap with PAHs and give rise to a pronounced IFE. Subtle structural differences in copolymer structure result in distinct spectral signatures, which provide a unique “chemical fingerprint” for each PAH. The discriminatory power of the array was evaluated using linear discriminant analysis (LDA) and principal component analysis (PCA) in order to discriminate between 16 PAH compounds identified as priority pollutants by the US Environmental Protection Agency (EPA). This array is the first multivariate system reliant on the modulation of the spectral signatures of CPs through the IFE for the detection and discrimination of closely related polynuclear aromatic species. |
format | Online Article Text |
id | pubmed-7020785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-70207852020-02-27 A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect Tropp, Joshua Ihde, Michael H. Williams, Abagail K. White, Nicholas J. Eedugurala, Naresh Bell, Noel C. Azoulay, Jason D. Bonizzoni, Marco Chem Sci Chemistry Natural and anthropogenic activities result in the production of polycyclic aromatic hydrocarbons (PAHs), persistent pollutants that negatively impact the environment and human health. Rapid and reliable methods for the detection and discrimination of these compounds remains a technological challenge owing to their relatively featureless properties, structural similarities, and existence as complex mixtures. Here, we demonstrate that the inner filter effect (IFE), in combination with conjugated polymer (CP) array-based sensing, offers a straightforward approach for the quantitative and qualitative profiling of PAHs. The sensor array was constructed from six fluorescent fluorene-based copolymers, which incorporate side chains with peripheral 2-phenylbenzimidazole substituents that provide spectral overlap with PAHs and give rise to a pronounced IFE. Subtle structural differences in copolymer structure result in distinct spectral signatures, which provide a unique “chemical fingerprint” for each PAH. The discriminatory power of the array was evaluated using linear discriminant analysis (LDA) and principal component analysis (PCA) in order to discriminate between 16 PAH compounds identified as priority pollutants by the US Environmental Protection Agency (EPA). This array is the first multivariate system reliant on the modulation of the spectral signatures of CPs through the IFE for the detection and discrimination of closely related polynuclear aromatic species. Royal Society of Chemistry 2019-10-07 /pmc/articles/PMC7020785/ /pubmed/32110311 http://dx.doi.org/10.1039/c9sc03405f Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Tropp, Joshua Ihde, Michael H. Williams, Abagail K. White, Nicholas J. Eedugurala, Naresh Bell, Noel C. Azoulay, Jason D. Bonizzoni, Marco A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect |
title | A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect
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title_full | A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect
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title_fullStr | A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect
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title_full_unstemmed | A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect
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title_short | A sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect
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title_sort | sensor array for the discrimination of polycyclic aromatic hydrocarbons using conjugated polymers and the inner filter effect |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020785/ https://www.ncbi.nlm.nih.gov/pubmed/32110311 http://dx.doi.org/10.1039/c9sc03405f |
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