Space-confined indicator displacement assay inside a metal–organic framework for fluorescence turn-on sensing
The indicator displacement assay (IDA) is for the first time performed within a metal–organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr( iv ) ion MOF (UiO-67-DQ–PsO) furnished with electron-deficient diquat units (DQ 2+ , as the receptor) on the wall and electron-r...
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| Published in | Chemical science (Cambridge) Vol. 10; no. 11; pp. 3307 - 3314 |
|---|---|
| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Royal Society of Chemistry
21.03.2019
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| Subjects | |
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| Abstract | The indicator displacement assay (IDA) is for the first time performed within a metal–organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr(
iv
) ion MOF (UiO-67-DQ–PsO) furnished with electron-deficient diquat units (DQ
2+
, as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO
−
, as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO
−
–DQ
2+
and alkylamine–DQ
2+
charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO
−
to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials. |
|---|---|
| AbstractList | The indicator displacement assay (IDA) is for the first time performed within a metal–organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr(iv) ion MOF (UiO-67-DQ–PsO) furnished with electron-deficient diquat units (DQ2+, as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO−, as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO−–DQ2+ and alkylamine–DQ2+ charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO− to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials. The indicator displacement assay (IDA) is for the first time performed within a metal-organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr(iv) ion MOF (UiO-67-DQ-PsO) furnished with electron-deficient diquat units (DQ , as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO , as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO -DQ and alkylamine-DQ charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials. The indicator displacement assay (IDA) is for the first time performed within a metal-organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr(iv) ion MOF (UiO-67-DQ-PsO) furnished with electron-deficient diquat units (DQ2+, as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO-, as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO--DQ2+ and alkylamine-DQ2+ charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO- to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials.The indicator displacement assay (IDA) is for the first time performed within a metal-organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr(iv) ion MOF (UiO-67-DQ-PsO) furnished with electron-deficient diquat units (DQ2+, as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO-, as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO--DQ2+ and alkylamine-DQ2+ charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO- to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials. The indicator displacement assay (IDA) is for the first time performed within a metal–organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr( iv ) ion MOF (UiO-67-DQ–PsO) furnished with electron-deficient diquat units (DQ 2+ , as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO − , as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO − –DQ 2+ and alkylamine–DQ 2+ charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO − to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials. Taking advantage of space-confined competing supramolecular interactions, the indicator displacement assay was performed within a recyclable MOF, which allows for fluorescence turn-on sensing with dramatically improved sensitivity and anti-interference The indicator displacement assay (IDA) is for the first time performed within a metal–organic framework (MOF) to achieve ultrasensitive fluorescence turn-on sensing. A Zr( iv ) ion MOF (UiO-67-DQ–PsO) furnished with electron-deficient diquat units (DQ 2+ , as the receptor) on the wall and electron-rich 1-pyrenesulfonate anions (PsO – , as the fluorescent indicator) in the pores was prepared by postsynthetic anion exchange. The MOF is capable of sensing alkylamines owing to the competing PsO – –DQ 2+ and alkylamine–DQ 2+ charge-transfer interactions, the former interaction causing a fluorescence OFF state and the latter displacing PsO – to trigger its emission. Significant advantages have been demonstrated for the IDA inside the MOF. The turn-on assay exhibits much higher sensitivity and anti-interference than the turn-off sensing using the MOF without indicators (the sensitivity is enhanced by as much as six orders of magnitude to the subnanomolar level). The integration of both the receptor and indicator in the porous solid enables facile regeneration and recyclability of the IDA ensemble. Furthermore, we show that the confined space provided by the MOF significantly enhances the supramolecular interactions to make possible the IDA impossible in solution. This work not only demonstrates a novel conceptual approach to fabricate superior fluorescence turn-on sensors using porous materials but also has important implications for supramolecular chemistry in porous materials. |
| Author | Yang, Ning-Ning Li, Peng Sui, Qi Gao, En-Qing Zhou, Li-Jiao |
| AuthorAffiliation | a Shanghai Key Laboratory of Green Chemistry and Chemical Processes , School of Chemistry and Molecular Engineering , East China Normal University , Shanghai 200062 , P. R. China . Email: eqgao@chem.ecnu.edu.cn |
| AuthorAffiliation_xml | – name: a Shanghai Key Laboratory of Green Chemistry and Chemical Processes , School of Chemistry and Molecular Engineering , East China Normal University , Shanghai 200062 , P. R. China . Email: eqgao@chem.ecnu.edu.cn |
| Author_xml | – sequence: 1 givenname: Ning-Ning surname: Yang fullname: Yang, Ning-Ning organization: Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, P. R. China – sequence: 2 givenname: Li-Jiao surname: Zhou fullname: Zhou, Li-Jiao organization: Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, P. R. China – sequence: 3 givenname: Peng surname: Li fullname: Li, Peng organization: Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, P. R. China – sequence: 4 givenname: Qi surname: Sui fullname: Sui, Qi organization: Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, P. R. China – sequence: 5 givenname: En-Qing orcidid: 0000-0002-5631-2391 surname: Gao fullname: Gao, En-Qing organization: Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, P. R. China |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30996917$$D View this record in MEDLINE/PubMed |
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| Snippet | The indicator displacement assay (IDA) is for the first time performed within a metal–organic framework (MOF) to achieve ultrasensitive fluorescence turn-on... The indicator displacement assay (IDA) is for the first time performed within a metal-organic framework (MOF) to achieve ultrasensitive fluorescence turn-on... Taking advantage of space-confined competing supramolecular interactions, the indicator displacement assay was performed within a recyclable MOF, which allows... |
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| SubjectTerms | Alkylamines Anion exchanging Assaying Charge transfer Chemistry Confined spaces Detection Displacement Fluorescent indicators Metal-organic frameworks Organic chemistry Porous materials Recyclability Regeneration Sensitivity enhancement Zirconium |
| Title | Space-confined indicator displacement assay inside a metal–organic framework for fluorescence turn-on sensing |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/30996917 https://www.proquest.com/docview/2190699391 https://www.proquest.com/docview/2211329363 https://pubmed.ncbi.nlm.nih.gov/PMC6428140 |
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