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Sensitive and fast fluorescence-based indirect sensing of TATP

Sensing of TATP vapours via the decomposition product, hydrogen peroxide, was achieved using a fluorescence “turn-on” mechanism through conversion of boronate esters to phenoxides under basic conditions in solid-state films. High sensitivity was achieved with two new fluorenylboronate esters compris...

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Detalles Bibliográficos
Autores principales: Fan, Shengqiang, Burn, Paul L., Shaw, Paul E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061106/
https://www.ncbi.nlm.nih.gov/pubmed/35518488
http://dx.doi.org/10.1039/c9ra00693a
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author Fan, Shengqiang
Burn, Paul L.
Shaw, Paul E.
author_facet Fan, Shengqiang
Burn, Paul L.
Shaw, Paul E.
author_sort Fan, Shengqiang
collection PubMed
description Sensing of TATP vapours via the decomposition product, hydrogen peroxide, was achieved using a fluorescence “turn-on” mechanism through conversion of boronate esters to phenoxides under basic conditions in solid-state films. High sensitivity was achieved with two new fluorenylboronate esters comprising either 2,4-difluorophenyl or 4-(trifluoromethyl)phenyl substituents. The key to the sensitivity was the fact that the phenoxide anion products from the hydrogen peroxide oxidation absorbed at longer wavelengths than the starting boronate esters. Selective excitation of the phenoxide anions avoided the background fluorescence from the corresponding boronate esters. The use of the electron withdrawing substituents also led to greater photostability. The derivative containing the 4-(trifluoromethyl)phenyl moiety was found to give the most stable phenoxide, and demonstrated fast fluorescence “turn-on” kinetics with a lower limit of detection of ≈2.5 ppb in 60 s.
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spelling pubmed-90611062022-05-04 Sensitive and fast fluorescence-based indirect sensing of TATP Fan, Shengqiang Burn, Paul L. Shaw, Paul E. RSC Adv Chemistry Sensing of TATP vapours via the decomposition product, hydrogen peroxide, was achieved using a fluorescence “turn-on” mechanism through conversion of boronate esters to phenoxides under basic conditions in solid-state films. High sensitivity was achieved with two new fluorenylboronate esters comprising either 2,4-difluorophenyl or 4-(trifluoromethyl)phenyl substituents. The key to the sensitivity was the fact that the phenoxide anion products from the hydrogen peroxide oxidation absorbed at longer wavelengths than the starting boronate esters. Selective excitation of the phenoxide anions avoided the background fluorescence from the corresponding boronate esters. The use of the electron withdrawing substituents also led to greater photostability. The derivative containing the 4-(trifluoromethyl)phenyl moiety was found to give the most stable phenoxide, and demonstrated fast fluorescence “turn-on” kinetics with a lower limit of detection of ≈2.5 ppb in 60 s. The Royal Society of Chemistry 2019-03-01 /pmc/articles/PMC9061106/ /pubmed/35518488 http://dx.doi.org/10.1039/c9ra00693a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Fan, Shengqiang
Burn, Paul L.
Shaw, Paul E.
Sensitive and fast fluorescence-based indirect sensing of TATP
title Sensitive and fast fluorescence-based indirect sensing of TATP
title_full Sensitive and fast fluorescence-based indirect sensing of TATP
title_fullStr Sensitive and fast fluorescence-based indirect sensing of TATP
title_full_unstemmed Sensitive and fast fluorescence-based indirect sensing of TATP
title_short Sensitive and fast fluorescence-based indirect sensing of TATP
title_sort sensitive and fast fluorescence-based indirect sensing of tatp
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061106/
https://www.ncbi.nlm.nih.gov/pubmed/35518488
http://dx.doi.org/10.1039/c9ra00693a
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