Fluorescent Sensors For Metal Ions Research Articles

Ratiometric Fluorescent Sensor for Copper(II) and Phosphate Ions from Aminopyrene Derivatives.

Three derivatives of 1-aminopyrene are functionalized with 2-picolyl and 2-picolinyl groups and are tested as fluorescent sensors for metal ions. The target compounds are successfully synthesized in yields of 50-90% and characterized by 1 H-NMR, 13 C-NMR, and HRMS. The compound with an amino picolyl group (P1) exhibits an excellent selectivity toward Cu(II) ion as the fluorescent signal shifts from 433 to 630 nm. From a fluorescence titration experiment, the limit of detection for Cu(II) ion is estimated as 0.19 µm. The fluorescence spectral shift by Cu(II) ion is reliant on the use of acetonitrile as a co-solvent, and the results from cyclic voltammetry and UV-Vis spectroscopy suggest that the sensing mechanism involves a coordination complex between the P1, acetonitrile and Cu(II) ion. Furthermore, this P1-Cu complex can also be used as a selective fluorescent sensor for PO4 3- ion with a detection limit of 0.44 µm.

DNAzyme-Mediated Genetically Encoded Sensors for Ratiometric Imaging of Metal Ions in Living Cells.

Genetically encoded fluorescent proteins (FPs) have been used for metal ion detection. However, their applications are restricted to a limited number of metal ions owing to the lack of available metal-binding proteins or peptides that can be fused to FPs and the difficulty in transforming the binding of metal ions into a change of fluorescent signal. We report herein the use of Mg2+-specific 10-23 or Zn2+-specific 8-17 RNA-cleaving DNAzymes to regulate the expression of FPs as a new class of ratiometric fluorescent sensors for metal ions. Specifically, we demonstrate the use of DNAzymes to suppress the expression of Clover2, a variant of the green FP (GFP), by cleaving the mRNA of Clover2, while the expression of Ruby2, a mutant of the red FP (RFP), is not affected. The Mg2+ or Zn2+ in HeLa cells can be detected using both confocal imaging and flow cytometry. Since a wide variety of metal-specific DNAzymes can be obtained, this method can likely be applied to imaging many other metal ions, expanding the range of the current genetically encoded fluorescent protein-based sensors.

DNAzyme-Mediated Genetically Encoded Sensors for Ratiometric Imaging of Metal Ions in Living Cells.

Genetically encoded fluorescent proteins (FPs) have been used for metal ion detection. However, their applications are restricted to a limited number of metal ions owing to the lack of available metal-binding proteins or peptides that can be fused to FPs and the difficulty in transforming the binding of metal ions into a change of fluorescent signal. We report herein the use of Mg2+ -specific 10-23 or Zn2+ -specific 8-17 RNA-cleaving DNAzymes to regulate the expression of FPs as a new class of ratiometric fluorescent sensors for metal ions. Specifically, we demonstrate the use of DNAzymes to suppress the expression of Clover2, a variant of the green FP (GFP), by cleaving the mRNA of Clover2, while the expression of Ruby2, a mutant of the red FP (RFP), is not affected. The Mg2+ or Zn2+ in HeLa cells can be detected using both confocal imaging and flow cytometry. Since a wide variety of metal-specific DNAzymes can be obtained, this method can likely be applied to imaging many other metal ions, expanding the range of the current genetically encoded fluorescent protein-based sensors.

Graphene quantum dots obtained by unfolding fullerene

Graphene quantum dots (GQDs) have recently been proposed as fluorescent sensors for metal ions dissolved in water. The physical origin of this fluorescence is still not completely clear, therefore further studies on GQDs and their properties are required. Graphene-like quantum dots were prepared by oxidation and unfolding of commercial buckminsterfullerene. This process was carried out by a modified Hummers method. After dialysis, the solution was diluted with deionized water to obtain the reference solution for optical measurements. Part of the solution was dried to obtain the unfolded fullerene powder. The metal ions were allowed to interact with GQDs by adding the metal-salt water solution to the stock solution of unfolded fullerene. The properties of GQDs before and after incorporation of metal ions (Hg, Cd, Pb, Cu, Ni and As) were characterized by using X-ray photoemission spectroscopy (XPS), Auger electron spectroscopy, UV–vis and fluorescent spectroscopies. In XPS, a particular attention was given to the analysis of photoemission C 1 s and Auger C KVV spectra in order to determine the carbon electronic configuration and its changes after incorporation of metal ions into GQDs. Obtained quantum dots were composed of graphene with oxidized borders. Optical measurements showed that the interaction with metal ions was changing the fluorescence intensity and optical absorbance, with different characteristics for each distinct ionic species. This behavior could be used for a selective multiple sensor detecting different heavy metals in water solutions.

Ethynylpyrene Linked Benzocrown Ethers as Fluorescent Sensors for Metal Ions.

Substances containing ethynylpyrenes linked to either one or four benzocrown ethers were synthesized, and their absorption and fluorescence spectroscopic responses to metal ions were assessed. Addition of metal perchlorates to solutions of these substances promotes short wavelength shifts in their absorption and fluorescence maxima and increases in their fluorescence intensities. The magnitudes of the fluorescence intensity increases are dependent on the ring size and number of the crown ether and the nature of the metal cation. Association constants for complex formation were calculated using fluorescence intensity versus concentration data. Analysis using Job's plots showed that the substances containing one benzocrown ether moiety form 1:1 complexes with metal ions. Results of experiments employing repeated addition and removal of Mg(ClO4 )2 demonstrate that the ON-OFF fluorescence response can be repeated at least three times. Results of molecular orbital calculations show that complexation with metal ions lowers the energies of both the π and π* levels of the ethynylpyrene moiety and that in some cases the vacant orbital on the metal becomes the LUMO of the complex. An explanation of the spectroscopic changes promoted by metal ions is proposed in terms of electrostatic repulsion and structural regulation.

Chelating Rotaxane Ligands as Fluorescent Sensors for Metal Ions

AbstractAlthough metal‐ion‐binding interlocked molecules have been under intense investigation for over three decades, their application as scaffolds for the development of sensors for metal ions remains underexplored. In this work, we demonstrate the potential of simple rotaxanes as metal‐ion‐responsive ligand scaffolds through the development of a proof‐of‐concept selective sensor for Zn2+.

Chelating Rotaxane Ligands as Fluorescent Sensors for Metal Ions.

Although metal‐ion‐binding interlocked molecules have been under intense investigation for over three decades, their application as scaffolds for the development of sensors for metal ions remains underexplored. In this work, we demonstrate the potential of simple rotaxanes as metal‐ion‐responsive ligand scaffolds through the development of a proof‐of‐concept selective sensor for Zn2+.

Should ACS Sensors Publish Papers on Fluorescent Sensors for Metal Ions at All?

Should <i>ACS Sensors</i> Publish Papers on Fluorescent Sensors for Metal Ions at All?

Highly stable ionic liquid-in-water emulsions as a new class of fluorescent sensors for metal ions: the case study of Fe3+ sensing

A stable fluorescent ionic liquid can act as a fluorescent sensor for metal ion recognition.

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores

Molecular cruciforms are X-shaped systems in which two conjugation axes intersect at a central core. If one axis of these molecules is substituted with electron-donors, and the other with electron-acceptors, cruciforms' HOMO will localize along the electron-rich and LUMO along the electron-poor axis. This spatial isolation of cruciforms' frontier molecular orbitals (FMOs) is essential to their use as sensors, since analyte binding to the cruciform invariably changes its HOMO-LUMO gap and the associated optical properties. Using this principle, Bunz and Miljanić groups developed 1,4-distyryl-2,5-bis(arylethynyl)benzene and benzobisoxazole cruciforms, respectively, which act as fluorescent sensors for metal ions, carboxylic acids, boronic acids, phenols, amines, and anions. The emission colors observed when these cruciform are mixed with analytes are highly sensitive to the details of analyte's structure and - because of cruciforms' charge-separated excited states - to the solvent in which emission is observed. Structurally closely related species can be qualitatively distinguished within several analyte classes: (a) carboxylic acids; (b) boronic acids, and (c) metals. Using a hybrid sensing system composed from benzobisoxazole cruciforms and boronic acid additives, we were also able to discern among structurally similar: (d) small organic and inorganic anions, (e) amines, and (f) phenols. The method used for this qualitative distinction is exceedingly simple. Dilute solutions (typically 10(-6) M) of cruciforms in several off-the-shelf solvents are placed in UV/Vis vials. Then, analytes of interest are added, either directly as solids or in concentrated solution. Fluorescence changes occur virtually instantaneously and can be recorded through standard digital photography using a semi-professional digital camera in a dark room. With minimal graphic manipulation, representative cut-outs of emission color photographs can be arranged into panels which permit quick naked-eye distinction among analytes. For quantification purposes, Red/Green/Blue values can be extracted from these photographs and the obtained numeric data can be statistically processed.

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores

Molecular cruciforms are X-shaped systems in which two conjugation axes intersect at a central core. If one axis of these molecules is substituted with electron-donors, and the other with electron-acceptors, cruciforms' HOMO will localize along the electron-rich and LUMO along the electron-poor axis. This spatial isolation of cruciforms' frontier molecular orbitals (FMOs) is essential to their use as sensors, since analyte binding to the cruciform invariably changes its HOMO-LUMO gap and the associated optical properties. Using this principle, Bunz and Miljanić groups developed 1,4-distyryl-2,5-bis(arylethynyl)benzene and benzobisoxazole cruciforms, respectively, which act as fluorescent sensors for metal ions, carboxylic acids, boronic acids, phenols, amines, and anions. The emission colors observed when these cruciform are mixed with analytes are highly sensitive to the details of analyte's structure and - because of cruciforms' charge-separated excited states - to the solvent in which emission is observed. Structurally closely related species can be qualitatively distinguished within several analyte classes: (a) carboxylic acids; (b) boronic acids, and (c) metals. Using a hybrid sensing system composed from benzobisoxazole cruciforms and boronic acid additives, we were also able to discern among structurally similar: (d) small organic and inorganic anions, (e) amines, and (f) phenols. The method used for this qualitative distinction is exceedingly simple. Dilute solutions (typically 10-6 M) of cruciforms in several off-the-shelf solvents are placed in UV/Vis vials. Then, analytes of interest are added, either directly as solids or in concentrated solution. Fluorescence changes occur virtually instantaneously and can be recorded through standard digital photography using a semi-professional digital camera in a dark room. With minimal graphic manipulation, representative cut-outs of emission color photographs can be arranged into panels which permit quick naked-eye distinction among analytes. For quantification purposes, Red/Green/Blue values can be extracted from these photographs and the obtained numeric data can be statistically processed.

ChemInform Abstract: New 7‐Hydroxycoumarin‐Based Fluorescent Chemosensors for Zn(II) and Cd(II).

AbstractFive new 7‐hydroxycoumarins (I) and (II) are synthesized and evaluated as fluorescent sensors for metal ions.

Hybrid sensor materials based on tin(IV) oxide and crown-containing 4-amino-1,8-naphthalimides

The cation-dependent spectral properties of crown-containing 4-aminonaphthalimide derivatives have been studied in an acetonitrile solution and within hybrid materials based on tin dioxide; these compounds can be of interest for producing fluorescent sensors for metal ions.

A Copper(II) Ion-Selective On−Off-Type Fluoroionophore Based on Zinc Porphyrin−Dipyridylamino

A new copper(II) fluorescent sensor 5,10,15,20-tetra((p-N,N-bis(2-pyridyl)amino)phenyl)porphyrin zinc (1) has been designed and synthesized by the Ullmann-type condensation of bromoporphyrin zinc with 2,2'-dipyridylamine (dpa) under copper powder as a catalyst as well as with K2CO3 as the base in a DMF solution. It consists of two separately functional moieties: the zinc porphyrin performs as a fluorophore, and the dpa-linked-to-zinc porphyrin acts as a selected binding site for metal ions. It displays a high selectivity and antidisturbance for the Cu2+ ion among the metal ions examined (Na+, Mg2+, Cr3+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Ag+, Zn2+, Cd2+, Hg2+, and Fe3+) and exhibits fluorescence quenching upon the binding of the Cu2+ ion with an "on-off"-type fluoroionophoric switching property. The detection limit is found to be 3.3 x 10(-7) M (3s blank) for Cu2+ ion in methanol solution, and its fluorescence can be revived by the addition of EDTA disodium solution. The design strategy and remarkable photophysical properties of sensor 1 help to extend the development of fluorescent sensors for metal ions.

Selective and Sensitive Fluorescent Sensors for Metal Ions Based on Manipulation of Side-Chain Compositions of Poly(p-phenyleneethynylene)s

The syntheses and metal-responsive properties of poly(p-phenyleenethynylene)s with grafted new pseudo-crown-ether groups are reported. These polymers exhibit high sensitivities to alkali ions because of their collective optical properties, which are very sensitive to ion-induced conformational changes. The quenching of polymer fluorescence caused by the conformational changes is proportional to the ion concentration. The selectivity of the sensing materials toward Li(+) ions is significantly enhanced by controlling the size of the binding site via manipulation of the polymer side-chain compositions. The polymers are very stable for their six-month solid-state storage at room temperature.

ChemInform Abstract: Dansylated Polyamines as Fluorescent Sensors for Metal Ions: Photophysical Properties and Stability of Copper(II) Complexes in Solution.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Dansylated Polyamines as Fluorescent Sensors for Metal Ions: Photophysical Properties and Stability of Copper(II) Complexes in Solution

Protonation and the CuII complexation constants of the dansylated polyamines N-dansylethylenediamine (1), N-dansyldiethylenetriamine (2), N-dansyltriethylenetetramine (3), N′-[2-(dansylamino)ethyl]diethylenetriamine (4), and tris(2-dansylaminoethyl)amine (5) were determined by glass-electrode potentiometry in MeOH/H2O 9 : 1 (v/v) solution. For ligands 3 and 4, the determinations were also performed in aqueous solution. The complexes formed by these ligands in neutral form correspond to those observed for the analogous unsubstituted monoprotonated amines, whereas, when the ligands are deprotonated at the sulfonamide moiety, the species parallel those of the corresponding amines. The molecular structures of the complexes were deduced from the VIS absorption spectra. The crystal structure of the [CuL2H−2] complex 6 of ligand 1 (L) was determined by X-ray diffraction. The study of the photophysical properties of the ligands 3 – 5 showed that they are good fluorescent sensors for copper(II), which induced fluorescence quenching. Time-resolved fluorescence measurements allowed us to clarify the sensing mechanism. The pH dependence of the quenching effect demonstrated that it occurs for all Cu2+ complexes, even for species in which the sulfonamide moiety is not deprotonated. Sensing of Cu2+ was compared with that of other metal ions (Co2+, Ni2+, Zn2+, Cd2+, Hg2+), and selectivity was studied as a function of pH. Ligands 3 and 4 were found to be selective chemosensors for Cu2+ in weakly acidic solution (pH ca. 4 – 5).