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A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water

A V-Shaped 4-amino-1,8-napthalimide derived tetracarboxylic acid linker (L; bis-[N-(1,3-benzenedicarboxylic acid)]-9,18-methano-1,8-naphthalimide-[b,f][1,5]diazocine) comprising the Tröger's base (TB) structural motif was rationally designed and synthesised to access a nitrogen-rich fluorescent...

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Autores principales: Shanmugaraju, Sankarasekaran, Dabadie, Charlyne, Byrne, Kevin, Savyasachi, Aramballi J., Umadevi, Deivasigamani, Schmitt, Wolfgang, Kitchen, Jonathan A., Gunnlaugsson, Thorfinnur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452275/
https://www.ncbi.nlm.nih.gov/pubmed/28572910
http://dx.doi.org/10.1039/c6sc04367d
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author Shanmugaraju, Sankarasekaran
Dabadie, Charlyne
Byrne, Kevin
Savyasachi, Aramballi J.
Umadevi, Deivasigamani
Schmitt, Wolfgang
Kitchen, Jonathan A.
Gunnlaugsson, Thorfinnur
author_facet Shanmugaraju, Sankarasekaran
Dabadie, Charlyne
Byrne, Kevin
Savyasachi, Aramballi J.
Umadevi, Deivasigamani
Schmitt, Wolfgang
Kitchen, Jonathan A.
Gunnlaugsson, Thorfinnur
author_sort Shanmugaraju, Sankarasekaran
collection PubMed
description A V-Shaped 4-amino-1,8-napthalimide derived tetracarboxylic acid linker (L; bis-[N-(1,3-benzenedicarboxylic acid)]-9,18-methano-1,8-naphthalimide-[b,f][1,5]diazocine) comprising the Tröger's base (TB) structural motif was rationally designed and synthesised to access a nitrogen-rich fluorescent supramolecular coordination polymer. By adopting the straight forward precipitation method, a new luminescent nanoscale Zn(ii) coordination polymer (TB-Zn-CP) was synthesized in quantitative yield using Zn(OAc)(2)·2H(2)O and tetraacid linker L (1 : 0.5) in DMF at room temperature. The phase-purity of as-synthesised TB-Zn-CP was confirmed by X-ray powder diffraction analysis, infra-red spectroscopy, and elemental analysis. Thermogravimetric analysis suggests that TB-Zn-CP is thermally stable up to 330 °C and the morphological features of TB-Zn-CP was analysed by SEM and AFM techniques. The N(2) adsorption isotherm of thermally activated TB-Zn-CP at 77 K revealed a type-II reversible adsorption isotherm and the calculated Brunauer–Emmett–Teller (BET) surface area was found to be 72 m(2) g(–1). Furthermore, TB-Zn-CP displayed an excellent CO(2) uptake capacity of 76 mg g(–1) at 273 K and good adsorption selectivity for CO(2) over N(2) and H(2). The aqueous suspension of as-synthesized TB-Zn-CP showed strong green fluorescence (λ (max) = 520 nm) characteristics due to the internal-charge transfer (ICT) transition and was used as a fluorescent sensor for the discriminative sensing of nitroaromatic explosives. The aqueous suspension of TB-Zn-CP showed the largest quenching responses with high selectivity for phenolic-nitroaromatics (4-NP, 2,4-DNP and PA) even in the concurrent presence of other potentially competing nitroaromatic analytes. The fluorescence titration studies also provide evidence that TB-Zn-CP detects picric acid as low as the parts per billion (26.3 ppb) range. Furthermore, the observed fluorescence quenching responses of TB-Zn-CP towards picric acid were highly reversible. The highly selective fluorescence quenching responses including the reversible detection efficiency make the nanoscale coordination polymer TB-Zn-CP a potential material for the discriminative fluorescent sensing of nitroaromatic explosives.
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spelling pubmed-54522752017-06-01 A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water Shanmugaraju, Sankarasekaran Dabadie, Charlyne Byrne, Kevin Savyasachi, Aramballi J. Umadevi, Deivasigamani Schmitt, Wolfgang Kitchen, Jonathan A. Gunnlaugsson, Thorfinnur Chem Sci Chemistry A V-Shaped 4-amino-1,8-napthalimide derived tetracarboxylic acid linker (L; bis-[N-(1,3-benzenedicarboxylic acid)]-9,18-methano-1,8-naphthalimide-[b,f][1,5]diazocine) comprising the Tröger's base (TB) structural motif was rationally designed and synthesised to access a nitrogen-rich fluorescent supramolecular coordination polymer. By adopting the straight forward precipitation method, a new luminescent nanoscale Zn(ii) coordination polymer (TB-Zn-CP) was synthesized in quantitative yield using Zn(OAc)(2)·2H(2)O and tetraacid linker L (1 : 0.5) in DMF at room temperature. The phase-purity of as-synthesised TB-Zn-CP was confirmed by X-ray powder diffraction analysis, infra-red spectroscopy, and elemental analysis. Thermogravimetric analysis suggests that TB-Zn-CP is thermally stable up to 330 °C and the morphological features of TB-Zn-CP was analysed by SEM and AFM techniques. The N(2) adsorption isotherm of thermally activated TB-Zn-CP at 77 K revealed a type-II reversible adsorption isotherm and the calculated Brunauer–Emmett–Teller (BET) surface area was found to be 72 m(2) g(–1). Furthermore, TB-Zn-CP displayed an excellent CO(2) uptake capacity of 76 mg g(–1) at 273 K and good adsorption selectivity for CO(2) over N(2) and H(2). The aqueous suspension of as-synthesized TB-Zn-CP showed strong green fluorescence (λ (max) = 520 nm) characteristics due to the internal-charge transfer (ICT) transition and was used as a fluorescent sensor for the discriminative sensing of nitroaromatic explosives. The aqueous suspension of TB-Zn-CP showed the largest quenching responses with high selectivity for phenolic-nitroaromatics (4-NP, 2,4-DNP and PA) even in the concurrent presence of other potentially competing nitroaromatic analytes. The fluorescence titration studies also provide evidence that TB-Zn-CP detects picric acid as low as the parts per billion (26.3 ppb) range. Furthermore, the observed fluorescence quenching responses of TB-Zn-CP towards picric acid were highly reversible. The highly selective fluorescence quenching responses including the reversible detection efficiency make the nanoscale coordination polymer TB-Zn-CP a potential material for the discriminative fluorescent sensing of nitroaromatic explosives. Royal Society of Chemistry 2017-02-01 2016-10-25 /pmc/articles/PMC5452275/ /pubmed/28572910 http://dx.doi.org/10.1039/c6sc04367d Text en This journal is © The Royal Society of Chemistry 2016 https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Shanmugaraju, Sankarasekaran
Dabadie, Charlyne
Byrne, Kevin
Savyasachi, Aramballi J.
Umadevi, Deivasigamani
Schmitt, Wolfgang
Kitchen, Jonathan A.
Gunnlaugsson, Thorfinnur
A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
title A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
title_full A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
title_fullStr A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
title_full_unstemmed A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
title_short A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
title_sort supramolecular tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452275/
https://www.ncbi.nlm.nih.gov/pubmed/28572910
http://dx.doi.org/10.1039/c6sc04367d
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