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

A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water
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 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)2·2H2O 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 N2 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 m2 g?1. Furthermore, TB-Zn-CP displayed an excellent CO2 uptake capacity of 76 mg g?1 at 273 K and good adsorption selectivity for CO2 over N2 and H2. The aqueous suspension of as-synthesized TB-Zn-CP showed strong green fluorescence (?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
1478-6524
1535-1546
Shanmugaraju, Sankarasekaran
193c398c-9ba6-4bc4-8204-ae483b9f9fda
Dabadie, Charlyne
5287c387-c7c7-4b41-87f9-5899c3243862
Byrne, Kevin
16399714-53a4-46b3-80e2-41cef34adc53
Savyasachi, Aramballi J.
a3f5b29f-18f5-49f6-b696-70a1dff8d57e
Umadevi, Deivasigamani
19dc078f-9a76-4a28-9cdf-82851a867cb2
Schmitt, Wolfgang
8b6c9507-b433-4f88-b96d-20424ff80864
Kitchen, Jonathan
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Gunnlaugsson, Thorfinnur
bbfcaaa6-2aca-47c9-9b7b-954442218f50
Shanmugaraju, Sankarasekaran
193c398c-9ba6-4bc4-8204-ae483b9f9fda
Dabadie, Charlyne
5287c387-c7c7-4b41-87f9-5899c3243862
Byrne, Kevin
16399714-53a4-46b3-80e2-41cef34adc53
Savyasachi, Aramballi J.
a3f5b29f-18f5-49f6-b696-70a1dff8d57e
Umadevi, Deivasigamani
19dc078f-9a76-4a28-9cdf-82851a867cb2
Schmitt, Wolfgang
8b6c9507-b433-4f88-b96d-20424ff80864
Kitchen, Jonathan
3999f5cb-d53e-4c51-b750-627bd2a1b9b6
Gunnlaugsson, Thorfinnur
bbfcaaa6-2aca-47c9-9b7b-954442218f50

Shanmugaraju, Sankarasekaran, Dabadie, Charlyne, Byrne, Kevin, Savyasachi, Aramballi J., Umadevi, Deivasigamani, Schmitt, Wolfgang, Kitchen, Jonathan and Gunnlaugsson, Thorfinnur (2016) A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water. Chemical Science, 8 (2), 1535-1546. (doi:10.1039/C6SC04367D).

Record type: Article

Abstract

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)2·2H2O 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 N2 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 m2 g?1. Furthermore, TB-Zn-CP displayed an excellent CO2 uptake capacity of 76 mg g?1 at 273 K and good adsorption selectivity for CO2 over N2 and H2. The aqueous suspension of as-synthesized TB-Zn-CP showed strong green fluorescence (?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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Accepted/In Press date: 24 October 2016
e-pub ahead of print date: 25 October 2016
Published date: 25 October 2016
Organisations: Organic Chemistry: SCF

Identifiers

Local EPrints ID: 403688
URI: http://eprints.soton.ac.uk/id/eprint/403688
ISSN: 1478-6524
PURE UUID: 001b1f90-1400-4fc4-b701-483f18994635
ORCID for Jonathan Kitchen: ORCID iD orcid.org/0000-0002-7139-5666

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Date deposited: 09 Dec 2016 08:56
Last modified: 15 Mar 2024 03:48

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Contributors

Author: Sankarasekaran Shanmugaraju
Author: Charlyne Dabadie
Author: Kevin Byrne
Author: Aramballi J. Savyasachi
Author: Deivasigamani Umadevi
Author: Wolfgang Schmitt
Author: Jonathan Kitchen ORCID iD
Author: Thorfinnur Gunnlaugsson

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