A highly selective colorimetric fluorescent probe for detection of Hg2+ and its application on test strips

An efficient fluorescent probe Pyr-Rhy based on pyrazole was developed, which can detect Hg²⁺ in water. Its fluorescence properties were studied by UV-vis and fluorescence spectroscopy, and the study results indicated that this probe can selectively detect Hg²⁺via complexation reaction, and then cause a remarkable color change from colorless to pink and a strong fluorescence enhancement can be observed. Furthermore, this probe showed high sensitivity with the detection limit down to 2.07 × 10⁻⁸ M, and its stoichiometric ratio toward Hg²⁺ ions was 1 : 1. The sensing mechanism was investigated by Job''s plot ¹H NMR titrations, and FT-IR spectra analysis, which demonstrated a chelation-enhanced fluorescence (CHEF) mechanism. More importantly, obvious color changes of sensor Pyr-Rhy can be observed when it was impregnated on filter paper testing strips and immersed in Hg²⁺ solution (water as solution), indicating its potential application for trace Hg²⁺ detection in environmental samples.

An efficient fluorescent probe Pyr-Rhy based on pyrazole was developed, which can detect Hg²⁺ in water.     

A colorimetric and fluorescent chemosensor for Hg2+ based on a photochromic diarylethene with a quinoline unit

A new colorimetric and fluorescent ‘on–off’ chemosensor, 1O, based on a photochromic diarylethene with a quinoline unit was designed and synthesized. The chemosensor 1O demonstrated selective and sensitive detection of Hg²⁺ ions in the presence of other competitive metal ions in acetonitrile. The stoichiometric ratio of the sensor 1O for Hg²⁺ was determined to be 1 : 1, and the limit of detection of the probe 1O was calculated to be 56.3 nM for Hg²⁺. In addition, a molecular logic circuit with four inputs and one output was successfully constructed with UV/vis light and metal-responsive behavior. ESI-MS spectroscopy, Job''s plot analysis, and ¹H NMR titration experiments confirm the binding behavior between 1O and Hg²⁺.

A new colorimetric and fluorescent ‘on–off’ chemosensor, 1O, based on a photochromic diarylethene with a quinoline unit was designed and synthesized.     

Bis-BODIPY linked-triazole based on catechol core for selective dual detection of Ag+ and Hg2+

Herein, we introduced a new chemosensor, bis-BODIPY linked-triazole based on catechol (BODIPY-OO) prepared by bridging two units of BODIPY fluorophore/triazole binding group with a catechol unit. A solution of this compound displayed 4- and 2-fold enhancements in fluorescence intensity after adding a mole equivalent amount of Ag⁺ and Hg²⁺ ions in methanol media, respectively. ¹H NMR titrations of BODIPY-OO with Ag⁺ and Hg²⁺ suggested that the triazole was involved in the recognition process. BODIPY-OO showed high sensitivity toward Ag⁺ and Hg²⁺ over other metal ions with detection limits of 0.45 μM and 1 μM, respectively. It can also distinguish Hg²⁺ from Ag⁺ by addition of an EDTA. This compound can therefore be employed as practical fluorescent probe for monitoring the presence of Ag⁺ and Hg²⁺ ions.

BODIPY–triazole–catechol combination serves as a “turn-on” fluorescent probe for dual detection and differentiation of Hg²⁺ and Ag⁺ ions.     

Rational design of fluorescent probe for Hg2+ by changing the chemical bond type

Two kinds of fluorescent probes DFBT and DFABT, and their corresponding water-soluble compounds WDFBT and WDFABT, based on the trimers containing a benzo[2,1,3]thiadiazole moiety and two fluorene moieties are synthesized. Their luminescent behavior towards Hg²⁺ ions and other various metal ions in organic and water solutions are studied in detail via absorption and emission spectroscopy. All these probes show a selective “on–off-type” fluorescent response to Hg²⁺ ions in solution over other metal ions with a maximum detection limit of 10⁻⁷ M. Importantly, the probe type can be changed from irreversible to reversible by altering the bridge mode between the functional units from C C triple bond to C–C single bond. Their detection mechanisms towards Hg²⁺ are studied in detail via mass spectrometry and Job plots, which are attributed to irreversible chemical reaction for DFABT and WDFABT and a reversible coordination reaction for DFBT and WDFBT respectively. Our research results about this kind of organic fluorescent probe provide valuable information to the future design of practical Hg²⁺ fluorescent probes.

Two kinds of fluorescent probes for Hg²⁺ with different detection mechanism have been realized by simply changing the chemical bond.     

A ratiometric and colorimetric probe for detecting Hg2+ based on naphthalimide–rhodamine and its staining function in cell imaging

In this work, a rhodamine derivative was developed as a colorimetric and ratiometric fluorescent probe for Hg²⁺. It exhibited a highly sensitive fluorescence response toward Hg²⁺. Importantly, studies revealed that the probe could be used for ratiometric detection of Hg²⁺, with a low detection limit of 0.679 μM. The mechanism of Hg²⁺ detection using compound 1 was confirmed by ESI-MS, ¹H NMR, and HPLC. Upon the addition of Hg²⁺, the rhodamine receptor was induced to be in the ring-opening form via an Hg²⁺-promoted hydrolysis of rhodamine hydrazide to rhodamine acid. In addition to Hg²⁺ detection, the naphthalimide–rhodamine compound was proven to be effective in cell imaging.

A new probe based on naphthalimide–rhodamine was applied in recognition of Hg²⁺ by a FRET mechanism.     

Sulfhydryl functionalized carbon quantum dots as a turn-off fluorescent probe for sensitive detection of Hg2+

Mercury ion (Hg²⁺) is one of the most toxic heavy metal ions and lowering the detection limit of Hg²⁺ is always a challenge in analytical chemistry and environmental analysis. In this work, sulfhydryl functionalized carbon quantum dots (HS-CQDs) were synthesized through a one-pot hydrothermal method. The obtained HS-CQDs were able to detect mercury ions Hg²⁺ rapidly and sensitively through fluorescence quenching, which may be ascribed to the formation of nonfluorescent ground-state complexes and electron transfer reaction between HS-CQDs and Hg²⁺. A modification of the HS-CQD surface by –SH was confirmed using Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The HS-CQDs sensing system obtained a good linear relationship over a Hg²⁺ concentration ranging from 0.45 μM to 2.1 μM with a detection limit of 12 nM. Delightfully, the sensor has been successfully used to detect Hg²⁺ in real samples with satisfactory results. This means that the sensor has the potential to be used for testing actual samples.

Schematic presentation of the synthesis of HS-CQDs and the application as a “turn-off” fluorescent probe for Hg²⁺ detection.     

A novel water-soluble naked-eye probe with a large Stokes shift for selective optical sensing of Hg2+ and its application in water samples and living cells

A water-soluble and colorimetric fluorescent probe with a large Stokes shift (139 nm) for rapidly detecting Hg²⁺, namely Hcy-mP, was synthesized by using an indole derivative and 2,4-dihydroxybenzaldehyde as starting materials. This probe demonstrates good selectivity for Hg²⁺ over other metal ions including Ag⁺, Pb²⁺, Cd²⁺, Cr³⁺, Zn²⁺, Fe³⁺, Co²⁺, Ni²⁺, Cu²⁺, K⁺, Na⁺, Mg²⁺, and Ca²⁺ in aqueous solution. With the increase in concentration of Hg²⁺, the color of the solution changed from pale yellow to pink and the fluorescence intensity decreased slightly. When 5-equivalents of EDTA were added to the solution with Hg²⁺, the fluorescence intensity of this probe was restored. The probe has been applied to the detection of Hg²⁺ in real water samples. Moreover, this probe was confirmed to have low cytotoxicity and excellent cell membrane permeability. The effect of Hcy-mP–Hg²⁺ towards living cells by confocal fluorescence was also investigated.

A water-soluble and colorimetric fluorescent probe with a large Stokes shift (139 nm) for rapidly detecting Hg²⁺, namely Hcy-mP, was synthesized by using an indole derivative and 2,4-dihydroxybenzaldehyde as starting materials.     

A reasonably constructed fluorescent chemosensor based on the dicyanoisophorone skeleton for the discriminative sensing of Fe3+ and Hg2+ as well as imaging in HeLa cells and zebrafish

In this study, a new fluorescent sensor dicyanoisophorone Rhodanine-3-acetic acid (DCI-RDA) (DCI-RDA) has been developed by employing a DCI-based push–pull dye as the fluorophore and RDA as the recognition moiety for the simultaneous sensing of Fe³⁺ and Hg²⁺ with a large Stokes Shift (162 nm), high selectivity and sensitivity, and low LOD (1.468 μM for Fe³⁺ and 0.305 μM for Hg²⁺). In particular, DCI-RDA has a short response time (30 s). The Job''s plot method in combination with ¹H NMR titration and theoretical calculations was used to determine the stoichiometry of both DCI-RDA-Fe³⁺/Hg²⁺ complexes to be 1 : 1. Moreover, DCI-RDA is applied as a fluorescent probe for imaging in HeLa cells and zebrafish, indicating that it can be potentially applied for Fe³⁺/Hg²⁺ sensing in the field of biology.

A new fluorescent sensor dicyanoisophorone rhodanine-3-acetic acid has been developed by employing a DCI-based push–pull dye as the fluorophore and RDA as the recognition moiety for the simultaneous sensing of Fe³⁺ and Hg²⁺.     

1,3,4-Thiadiazol derivative functionalized-Fe3O4@SiO2 nanocomposites as a fluorescent probe for detection of Hg2+ in water samples

5-Amino-1,3,4-thiadiazole-2-thiol was used to synthesize a novel fluorescent functionalizing group on a Fe₃O₄@SiO₂ magnetic nanocomposite surface for detection of heavy metal ions in water samples. The prepared probe was characterized by using X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and a vibrating sample magnetometer. Among various tested ions, the new nanocomposite responded to Hg²⁺ ions with an intense fluorescence “turn-off”. The limit of detection of the probe shows that it is sensitive to the minimum Hg²⁺ concentration of 48.7 nM. Theoretical calculations were done for estimating binding energies of the three possible bonding modes and the visualized molecular orbitals were presented.

VBYT-Fe₃O₄@SiO₂ fluorescent probe was designed for sensitive detection of mercury in water samples.     

Development of a fused imidazo[1,2-a]pyridine based fluorescent probe for Fe3+ and Hg2+ in aqueous media and HeLa cells

A new fluorescent sensor 5 based on a fused imidazopyridine scaffold has been designed and synthesized via cascade cyclization. The reaction features the formation of three different C–N bonds in sequence. Imidazopyridine based fluorescent probe 5 exhibits highly sensitive and selective fluorescent sensing for Fe³⁺(‘turn-on’) and Hg²⁺(‘turn-off’). The excellent selectivity of imidazopyridine for Fe³⁺/Hg²⁺ was not hampered in the presence of any of the competing cations. The limit of detection (LOD) of 5 toward Fe³⁺ and Hg²⁺ has been estimated to be 4.0 ppb and 1.0 ppb, respectively, with a good linear relationship (R² = 0.99). Notably, 5 selectively detects Fe³⁺/Hg²⁺ through fluorescence enhancement signalling both in vitro and in HeLa cells.

A new fluorescent sensor 5 having fused imidazopyridine scaffold has been synthesized via cascade cyclization. It exhibits highly sensitive and selective detection of Fe³⁺ (‘turn-on’) and Hg²⁺ (‘turn-off’) in vitro and in HeLa cells.     

A curcumin-based AIEE-active fluorescent probe for Cu2+ detection in aqueous solution

Curcuminoids have been extensively investigated as metal ion probes, but the intrinsic aggregation-caused-quenching (ACQ) characteristic of curcumin would hinder their applications in aqueous solution. Fortunately, tetraphenylethylene (TPE) could endow the compounds with aggregation-induced emission (AIE)/aggregation-induced enhanced emission (AIEE) characteristics to eliminate the ACQ effect. According to this strategy, a series of TPE-modified curcumin derivatives L1–4 were prepared and studied for their AIEE properties. Among the four TPE-curcumin analogues, only L1 particles have been successfully used as an on-off fluorescence probe for detecting Cu²⁺ in aqueous solution. The fluorescence titration experiment determined its detection limit of 1.49 × 10⁻⁷ mol L⁻¹, and the binding ratio between L1 and Cu²⁺ was estimated as 2 : 1, which was in agreement with the results of high resolution mass spectrum and Job''s plot. In addition, the binding constant was evaluated as 6.77 × 10² M⁻¹ using a Benesi–Hildebrand plot. Finally, the obtained L1-based indicator paper showed significant fluorescence response to Cu²⁺ aqueous solution. This TPE-modified strategy improves the detection capability of curcumin probe in aqueous solution and provides a feasible way to obtain other probes with ACQ characteristics.

A curcumin-based AIEE-active L1 was synthesized and used to prepare an on-off fluorescent probe for Cu²⁺ detection in aqueous solution.     

Colorimetric screening of elevated urinary mercury levels by a novel Hg2+-selective probe of resorufin phosphinothioate

Urinary mercury levels are the most reliable indicators of mercury exposure but identifying them requires complex techniques and heavy instruments. In this research, we reported a simple and convenient urinary mercury analysis method using a readily available office scanner. Probe MP-1 synthesized by the reaction of resorufin and dimethylthiophosphinoyl chloride revealed Hg²⁺-selective chromogenic and fluorescent signaling behavior. Signaling was realized through Hg²⁺-induced deprotection of the phosphinothioate protecting group in the resorufin-based probe MP-1 to yield the parent fluorochrome. A pronounced colorimetric response of color change from light yellow to pink alongside a turn-on type fluorescence enhancement was perceived exclusively toward Hg²⁺ ions over other metal ions and anions. The colorimetry provided a more advantageous ratiometric approach than the simple fluorometric analysis exhibiting an off–on type response, with a detection limit of 12 nM (2.4 ppb). The Hg²⁺ signaling of the MP-1 probe was not disturbed by the presence of coexisting metal ions and anions. The sensitive and convenient diagnosis of clinically important neurological symptoms and fatal inorganic mercury levels in urine was successfully demonstrated using a standard office scanner.

A Hg²⁺ selective signaling probe, resorufin phosphinothioate, for the colorimetric diagnosis of clinically elevated mercury levels in urine samples using an office scanner was developed.     

A novel coumarin-based colorimetric and fluorescent probe for detecting increasing concentrations of Hg2+in vitro and in vivo

Mercury has complex biological toxicity and can cause a variety of physiological diseases and even death, so it is of great importance to develop novel strategies for detecting trace mercury in environmental and biological samples. In this work, we designed a new coumarin-based colorimetric and fluorescent probe CNS, which could be obtained from inexpensive starting materials with high overall yield in three steps. Probe CNS could selectively respond to Hg²⁺ with obvious color and fluorescence changes, and the presence of other metal ions had no effect on the fluorescence changes. Probe CNS also exhibited high sensitivity against Hg²⁺, with a detection limit as low as 2.78 × 10⁻⁸ M. More importantly, the behavioral tracks of zebrafish had no obvious changes upon treatment with 10 μM probe CNS, thus indicating its low toxicity. The probe showed potential application value and was successfully used for detecting Hg²⁺ in a test strip, HeLa cells and living zebrafish larvae.

Mercury has complex biological toxicity and can cause a variety of physiological diseases and even death, so it is of great importance to develop novel strategies for detecting trace mercury in environmental and biological samples.     

Rapid electrochemical quantification of trace Hg2+ using a hairpin DNA probe and quantum dot modified screen-printed gold electrodes

Rapid, simple, sensitive and specific approaches for mercury(ii) (Hg²⁺) detection are essential for toxicology assessment, environmental protection, food analysis and human health. In this study, a ratiometric hairpin DNA probe based electrochemical biosensor, which relies on hairpin DNA probes conjugated with water-soluble and carboxyl functionalized quaternary Zn–Ag–In–S quantum dot (QD) on screen-printed gold electrodes (SPGE), referred to as the HP-QDs-SPGE electrochemical biosensor in this study, was developed for Hg²⁺ detection. Based on the “turn-off” reaction of a hairpin DNA probe binding with a mismatched target and Hg²⁺ through the formation of T–Hg²⁺–T coordination, the HP-QDs-SPGE electrochemical biosensor can rapidly quantify trace Hg²⁺ with high ultrasensitivity, specificity, repeatability and reproducibility. The conformational change of the hairpin DNA probe caused a significant decrease in electrochemical intensity, which could be used for the quantification of Hg²⁺. The linear dynamic range and high sensitivity of the HP-QDs-SPGE electrochemical biosensor for the detection of Hg²⁺ was studied in vitro, with a broad linear dynamic range of 10 pM to 1 μM and detection limits of 0.11 pM. In particular, this HP-QDs-SPGE electrochemical biosensor showed excellent selectivity toward Hg²⁺ ions in the presence of other metal ions. More importantly, this biosensor has been successfully used to detect Hg²⁺ in deionized water, tap water, groundwater and urine samples with good recovery rate and small relative standard deviations. In summary, the developed HP-QDs-SPGE electrochemical biosensor exhibited promising potential for further applications in on-site analysis.

A ratiometric hairpin DNA probe based electrochemical biosensor, which relies on hairpin DNA probes conjugated with water-soluble and carboxyl functionalized quantum dot on screen-printed gold electrodes, was developed for Hg²⁺ detection.     

A facile imine-linked covalent organic framework doped with a carbon dot composite for the detection and removal of Hg2+ in surface water

Hg²⁺ is one of the most toxic chemical species in the water environment, and thus developing a new fluorescent covalent organic framework for both the detection and removal of Hg²⁺ is highly desirable. Herein, a fluorescent composite, termed TpPa-1 COF@CDs, was synthesized by inverse emulsion polymerization method using an imine covalent organic framework as the supporting material and carbon dots as the fluorescent sensor element. The crystallinity, porosity, rich functional receptors (hydroxyl and amino groups), thermal stability and fluorescent properties of TpPa-1 COF@CDs were characterized. The results showed that TpPa-1 COF@CDs exhibited a good detection and removal performance for Hg²⁺, which was evidenced by its high sensitivity (LOD = 0.75 μg L⁻¹), superior selectivity, large adsorption capacity (235 mg g⁻¹), fast adsorption rate (30 min equilibrium time) and good regeneration (at least five cycles). More importantly, the simple functional monomer, short reaction time and metal-free raw material made TpPa-1 COF@CDs reliable, cost effective and eco-friendly. This research demonstrated the facile construction of a functional covalent organic framework composite for water environmental remediation technologies of metal pollution.

TpPa-1 COF@CDs as a fluorescent composite exhibited good detection and removal performance for Hg²⁺. The simple functional monomer, short reaction time and metal-free raw material made TpPa-1 COF@CDs reliable, cost effective and eco-friendly.     

Chemosensors based on N-heterocyclic dyes: advances in sensing highly toxic ions such as CN− and Hg2+

CN⁻ and Hg²⁺ ions are harmful to both the environment and human health, even at trace levels. Thus, alternative methods for their detection and quantification are highly desirable given that the traditional monitoring systems are expensive and require qualified personnel. Optical chemosensors (probes) have revolutionized the sensing of different species due to their high specificity and sensitivity, corresponding with their modular design. They have also been used in aqueous media and different pH ranges, facilitating their applications in various samples. The design of molecular probes is based on organic dyes, where the key species are N-heterocyclic compounds (NHCs) due to their proven photophysical properties, biocompatibility, and synthetic versatility, which favor diverse applications. Accordingly, this review aims to provide an overview of the reports from 2016 to 2021, in which fluorescent probes based on five- and six-membered N-heterocycles are used for the detection of CN⁻ and Hg²⁺ ions.

This review considers the most recent advances in sensing highly toxic ions such as CN⁻ and Hg²⁺. Specifically, probes bearing N-heterocyclic compounds for their proven versatility for applications in the development of chemosensors are analyzed.     

Synthesis,characterisation and ion-binding properties of oxathiacrown ethers appended to [Ru(bpy)2]2+. Selectivity towards Hg2+, Cd2+ and Pb2+

A series of complexes with oxathiacrown ethers appended to a [Ru(bpy)₂]²⁺ moiety have been synthesized and characterised using ¹H NMR, ¹³C NMR, IR, electronic absorption and emission spectroscopies, mass spectrometry and elemental analyses. The complexes exhibit strong MLCT luminescence bands in the range 608–611 nm and one reversible metal centred oxidation potential in the range 1.00–1.02 V. Their selectivity and sensitivity towards Hg²⁺, Cd²⁺ and Pb²⁺ metal ions have been investigated using electronic absorption, luminescence, cyclic and differential pulse voltammetry titrations. Their responses towards selected cations and anions have also been investigated using electronic absorption and luminescence. While the complexes are selective towards Hg²⁺ and Cd²⁺ ions, none of them is selective towards Pb²⁺ ions. In particular, complex 2 gives a selective change in the UV/Vis absorbance with Hg²⁺ making it possible to detect mercury down to a detection limit of 68 ppm. The binding constants and limits of detection of the complexes have been calculated, with values ranging from 4.37 to 5.38 and 1.4 × 10⁻³ to 6.8 × 10⁻⁵ for log K_s and LOD respectively.

Oxathiacrown ether modified ruthenium complex 2 facilitates a selective naked-eye detection of Hg²⁺ with an instrumental detection limit of 68 ppm.     

Two novel colorimetric fluorescent probes: Hg2+ and Al3+ in the visual colorimetric recognition environment

Two new dual channel Schiff base fluorescent probes, Tri-R6G and Tri-Flu, were synthesized, and can detect Hg²⁺ and Al³⁺, respectively. The two probes were characterized by FTIR, ¹H NMR, ¹³C NMR and HRMS, and their optical properties were detected by UV and FL. Test results showed the probes'' detection of Hg²⁺ and Al³⁺ compared to other metal ions (Ag⁺, Co²⁺, Cd²⁺, Mg²⁺, Cu²⁺, Ni²⁺, Ba²⁺, Pb²⁺, Cr³⁺, Al³⁺, Zn²⁺, Hg²⁺, K⁺, Ga²⁺ and Fe³⁺), respectively. Besides, the detection limits were determined to be 1.61 × 10⁻⁸ M and 1.15 × 10⁻⁸ M through the standard curve plot, respectively. The photoelectron transfer (PET) mechanism was guessed by the Job''s plot and the infrared titration. Corresponding orbital electron distribution and molecular geometry configurations of the compounds were predicted by density functional theory (DFT). In addition, the prepared test paper changed from white to pink when the target ion was detected. The color changed from colorless to pink in a solution having a concentration of 10⁻⁵ M.

Two new dual channel Schiff base fluorescent probes, Tri-R6G and Tri-Flu, were synthesized, and can detect Hg²⁺ and Al³⁺, respectively.     

A dual colorimetric probe for rapid environmental monitoring of Hg2+ and As3+ using gold nanoparticles functionalized with d-penicillamine

A highly sensitive and selective colorimetric assay for the dual detection of Hg²⁺ and As³⁺ using gold nanoparticles (AuNPs) conjugated with d-penicillamine (DPL) was developed. When Hg²⁺ and As³⁺ ions coordinate with AuNP-bound DPLs, the interparticle distance decreases, inducing aggregation; this results in a significant color change from wine red to dark midnight blue. The Hg4f and As3d signals in the X-ray photoelectron spectra of Hg²⁺ (As³⁺)-DPL-AuNPs presented binding energies indicative of Hg²⁺–N(O) and As³⁺–N(O) bonds, and the molecular fragment observed in time-of-flight secondary ion mass spectra confirmed that Hg²⁺ and As³⁺ coordinated with two oxygen and two nitrogen atoms in DPL. The detection of Hg²⁺ and As³⁺ can be accomplished by observing the color change with the naked eye or by photometric methods, and this was optimized to provide optimal probe sensitivity. The assay method can be applied for environmental monitoring by first selectively quantifying Hg²⁺ in water samples at pH 6, then estimating the As³⁺ concentration at pH 4.5. The efficiency of the DPL-AuNP probe was evaluated for the sequential quantification of Hg²⁺ and As³⁺ in tap, pond, waste, and river water samples, and absorbance ratios (A₇₃₀/A₅₂₅) were correlated with Hg²⁺ and As³⁺ concentrations in the linear range of 0–1.4 μM. The limits of detection in water samples were found to be 0.5 and 0.7 nM for Hg²⁺ and As³⁺, respectively. This novel probe can be utilized for the dual determination of Hg²⁺ and As³⁺, even in the presence of interfering substances in environmental samples.

A highly sensitive and selective colorimetric assay for the dual detection of Hg²⁺ and As³⁺ using gold nanoparticles (AuNPs) conjugated with d-penicillamine (DPL) was developed.     

A simple fluorescent probe for detection of Ag+ and Cd2+ and its Cd2+ complex for sequential recognition of S2−

In this study, we designed and synthesized a simple probe 2-(8-((8-methoxyquinolin-2-yl)methoxy)quinolin-2-yl)benzo[d]thiazole (DQT) for detection of Ag⁺ and Cd²⁺ in a CH₃OH/HEPES (9 : 1 v/v, pH = 7.30) buffer system. Its structure was characterized by NMR, ESI-HR-MS and DFT calculations, and its fluorescence performance was also investigated. Probe DQT showed fluorescence quenching in response to Ag⁺ and Cd²⁺ with low detection limits of 0.42 μM and 0.26 μM, respectively. Importantly, the complexation of the probe with Cd²⁺ resulted in a red shift from blue to green, making it possible to detect Ag⁺ and Cd²⁺ by the naked eye under an ultraviolet lamp. The DQT-Cd²⁺ complex could be used for sequential recognition of S²⁻. The recovery response could be repeated 3 times by alternate addition of Cd²⁺ and S²⁻. A filter paper strip test further demonstrated the potential of probe DQT as a convenient and rapid assay.

A fluorescent probe for detection of Ag⁺ and Cd²⁺ and its Cd²⁺ complex for sequential recognition of S²⁻.