The design of selective and sensitive chemosensor for sensing of biomolecules and phenol derivatives remains a significant challenge. Here, we report on the synthesis of a highly robust and thermally stable Zn-metal organic framework, via a hydrothermal reaction using 1,4-naphthalenedicarboxylic acid (H2L), 1,2-di(pyridin-4-yl) ethane (bpe), and Zn(ClO4)2 & sdot;6H2O. The resulting compound [Zn3(L2- )2(bpe)2] (Zn-MOF-1) was synthesized and characterized using elemental analysis, FT-IR, TGA, PXRD, XPS, and single-crystal X-ray diffraction. Singlecrystal analysis reveals that Zn-MOF-1 features a three-dimensional (3D) layered framework stabilized by C-H & sdot;& sdot;& sdot;O hydrogen bonding and pi-pi stacking interactions. Notably, the structure incorporates both distorted octahedral and pentagonal bipyramidal zinc coordination geometries within the same framework-an uncommon feature. Topological analysis confirms a (3,6)-connected, two-fold interpenetrated dia (diamondoid) network, underscoring the complexity and uniqueness of the structure. Given the excellent luminescent properties of Zn MOF-1, sensing experiments were conducted using various biomolecules. The results demonstrated selective molecular recognition of Ammonium ferric citrate (AF) and aspirin (ASP) by Zn-MOF-1, exhibiting a 'turn-off' luminescence response for AF and a 'turn-on' response for ASA. The limits of detection (LOD) were 4.573 x 10-5 mol/L for AF and 4.215 x 10-5 mol/L for ASA, with corresponding Stern-Volmer constants (Ksv) of 2563.29 M-1 and 2781.25 M-1, respectively. The practical applicability of this sensing approach was evaluated using real water samples. Real water sample tests gave recoveries of 95-102 %, confirming reliability. Timeresolved studies revealed a reduced fluorescence lifetime upon AF addition, confirming a dynamic quenching mechanism. Furthermore, analysis of the absorption and emission overlap suggested a contribution from the inner filter effect (IFE). After IFE correction, the results highlighted genuine molecular interactions between AF and Zn-MOF-1. This establishes Zn-MOF-1 as a sensitive and selective fluorescent sensor for environmental and bioanalytical applications.

A Zn(II)-based metal–organic framework as a turn-off/on fluorescent sensor for selective detection of ammonium ferric citrate and aspirin

Ansari, Istikhar A.;
2026

Abstract

The design of selective and sensitive chemosensor for sensing of biomolecules and phenol derivatives remains a significant challenge. Here, we report on the synthesis of a highly robust and thermally stable Zn-metal organic framework, via a hydrothermal reaction using 1,4-naphthalenedicarboxylic acid (H2L), 1,2-di(pyridin-4-yl) ethane (bpe), and Zn(ClO4)2 & sdot;6H2O. The resulting compound [Zn3(L2- )2(bpe)2] (Zn-MOF-1) was synthesized and characterized using elemental analysis, FT-IR, TGA, PXRD, XPS, and single-crystal X-ray diffraction. Singlecrystal analysis reveals that Zn-MOF-1 features a three-dimensional (3D) layered framework stabilized by C-H & sdot;& sdot;& sdot;O hydrogen bonding and pi-pi stacking interactions. Notably, the structure incorporates both distorted octahedral and pentagonal bipyramidal zinc coordination geometries within the same framework-an uncommon feature. Topological analysis confirms a (3,6)-connected, two-fold interpenetrated dia (diamondoid) network, underscoring the complexity and uniqueness of the structure. Given the excellent luminescent properties of Zn MOF-1, sensing experiments were conducted using various biomolecules. The results demonstrated selective molecular recognition of Ammonium ferric citrate (AF) and aspirin (ASP) by Zn-MOF-1, exhibiting a 'turn-off' luminescence response for AF and a 'turn-on' response for ASA. The limits of detection (LOD) were 4.573 x 10-5 mol/L for AF and 4.215 x 10-5 mol/L for ASA, with corresponding Stern-Volmer constants (Ksv) of 2563.29 M-1 and 2781.25 M-1, respectively. The practical applicability of this sensing approach was evaluated using real water samples. Real water sample tests gave recoveries of 95-102 %, confirming reliability. Timeresolved studies revealed a reduced fluorescence lifetime upon AF addition, confirming a dynamic quenching mechanism. Furthermore, analysis of the absorption and emission overlap suggested a contribution from the inner filter effect (IFE). After IFE correction, the results highlighted genuine molecular interactions between AF and Zn-MOF-1. This establishes Zn-MOF-1 as a sensitive and selective fluorescent sensor for environmental and bioanalytical applications.
2026
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Ammonium ferric citrate (AF)
Aspirin (ASA)
Fluorescent sensor
Molecular recognition
Zinc-based metal-organic frameworks
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/555323
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