Browse
Submit Data
Databases
API
Help

Dataset Information

36 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Selective Hg(II) detection in aqueous solution with thiol derivatized fluoresceins.

ABSTRACT: The syntheses and photophysical properties of mercury sensors 2 and 3 (MS2 and MS3), two asymmetrically derivatized fluorescein-based dyes designed for Hg(II) detection, are described. These sensors each contain a single pyridyl-amine-thiol metal-binding moiety, form 1:1 complexes with Hg(II), and exhibit selectivity for Hg(II) over other Group 12 metals, alkali and alkaline earth metals, and most divalent first-row transition metals. Both dyes display superior brightness (Phi x epsilon) and fluorescence enhancement following Hg(II) coordination in aqueous solution. At neutral pH, the fluorescence turn-on derives from greater brightness due to increased molar absorptivity. At higher pH, photoinduced electron transfer quenching of the free dye is enhanced, and the Hg(II)-induced turn-on also benefits from alleviation of this pathway. MS2 can detect ppb levels of Hg(II) in aqueous solution, demonstrating its ability to identify environmentally relevant concentrations of Hg(II).

SUBMITTER: Nolan EM

PROVIDER: S-EPMC2495028 | biostudies-literature | 2006 Mar

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Selective Hg(II) detection in aqueous solution with thiol derivatized fluoresceins.

Nolan Elizabeth M EM Racine Maryann E ME Lippard Stephen J SJ

Inorganic chemistry 20060301 6

The syntheses and photophysical properties of mercury sensors 2 and 3 (MS2 and MS3), two asymmetrically derivatized fluorescein-based dyes designed for Hg(II) detection, are described. These sensors each contain a single pyridyl-amine-thiol metal-binding moiety, form 1:1 complexes with Hg(II), and exhibit selectivity for Hg(II) over other Group 12 metals, alkali and alkaline earth metals, and most divalent first-row transition metals. Both dyes display superior brightness (Phi x epsilon) and flu ...[more]

PMID: 16529499

Similar Datasets

QZ1 and QZ2: rapid, reversible quinoline-derivatized fluoresceins for sensing biological Zn(II).

Project description:QZ1, 2-[2-chloro-6-hydroxy-3-oxo-5-(quinolin-8-ylaminomethyl)-3H-xanthen-9-yl]benzoic acid, and QZ2, 2-[6-hydroxy-3-oxo-4,5-bis-(quinolin-8-ylaminomethyl)-3H-xanthen-9-yl]benzoic acid, two fluorescein-based dyes derivatized with 8-aminoquinoline, have been prepared and their photophysical, thermodynamic, and zinc-binding kinetic properties determined. Because of their low background fluorescence and highly emissive Zn(II) complexes, QZ1 and QZ2 have a large dynamic range, with approximately 42- and approximately 150-fold fluorescence enhancements upon Zn(II) coordination, respectively. These dyes have micromolar K(d) values for Zn(II) and are selective for Zn(II) over biologically relevant concentrations of the alkali and alkaline earth metals. The Zn(II) complexes also fluoresce brightly in the presence of excess Mn(II), Fe(II), Co(II), Cd(II), and Hg(II), offering improved specificity for Zn(II) over di(2-picolyl)amine-based Zn(II) sensors. Stopped-flow kinetic investigations indicate that QZ1 and QZ2 bind Zn(II) with k(on) values of (3-4) x 10(6) M(-1) s(-1), compared to (6-8) x 10(5) M(-1) s(-1) for select ZP (Zinpyr) dyes, at 4.3 degrees C. Dissociation of Zn(II) from QZ1 and QZ2 occurs with k(off) values of 150 and 160 s(-1), over 5 orders of magnitude larger than those for ZP probes, achieving reversibility on the biological (millisecond) time scale. Laser scanning confocal and two-photon microscopy studies reveal that QZ2 is cell-permeable and Zn(II)-responsive in vivo. Because of its weaker affinity for Zn(II), QZ2 responds to higher concentrations of intracellular Zn(II) than members of the ZP family, illustrating that binding affinity is an important parameter for Zn(II) detection in vivo.

| S-EPMC1851667 | biostudies-literature

Biosorption of Hg (II) from aqueous solution using algal biomass: kinetics and isotherm studies.

Project description:The present work investigated the ability of algal biomass Chlorella vulgaris to remove mercury from aqueous solutions. The mercury biosorption process was studied through batch experiments 35 °C temperature with regard to the influence of contact time, initial mercury concentration, pH and desorption. The maximum adsorption capacity was registered at pH 6. The adsorption conduct of Hg(II) was defined by pseudo second order well rather pseudo first order as the experimental data (qe) come to an agreement with the calculated value. The kinetics of adsorption was fast and a high capacity of adsorption occurred within only 90 min. The adsorption data were signified by many models but Langmuir (qmax = 42. mg g-1) & Freundlich fitted well having regression coefficients near to unity. The thermodynamic parameters were also suited well as negative value of free energy cope up to spontaneity, positive value of the randomness described by ΔS attributed to affinity of Hg+2 towards algal bioadsorbant and high positive value of heat of enthalpy designates that the adsorption process is expected due to robust interactions between the Hg(II) ions and various functional groups on surface of algal bioadsorbant. Field emission scanning electron microscopy integrated with energy dispersive X-ray spectroscopy analysis before and after adsorption of Hg(II) reveals the adsorption of metallic ions over the surface. FTIR study supported the existence of various functional groups (carboxylix, amines, hydroxyls, amides etc.) helped in adsorption. Continuous adsorption desorption experiments proved that algal cells was excellent biosorbents with potential for further development.

| S-EPMC7000812 | biostudies-literature

Visual detection of Hg²⁺ in aqueous solution using gold nanoparticles and thymine-rich hairpin DNA probes.

Project description:We report a sensitive method for visual detection of mercury ions (II) (Hg²⁺) in aqueous solution by using gold nanoparticles (Au-NPs) and thymine (T)-rich hairpin DNA probes. The thiolated hairpin DNA probe was immobilized on the Au-NP surface through a self-assembling method. Another thymine-rich, digoxin-labeled DNA probe was introduced to form DNA duplexes on the Au-NP surface with thymine-Hg²⁺-thymine (T-Hg²⁺-T) coordination in the presence of Hg²⁺. The Au-NPs associated with the formed duplexes were captured on the test zone of a lateral flow strip biocomponent (LFSB) by immunoreaction events between the digoxin on the duplexes and anti-digoxin antibodies on the LFSB. The accumulation of Au-NPs produced a characteristic red band on the test zone, enabling visual detection of Hg²⁺ without instrumentation. A detection limit of 0.1 nM was obtained under optimal experimental conditions. This method provides a simple, rapid, sensitive approach for the detection of Hg²⁺ and shows great promise for point-of-care and in-field detection of environmentally toxic mercury.

| S-EPMC3220944 | biostudies-literature

A Zinc(II) Schiff Base Complex as Fluorescent Chemosensor for the Selective and Sensitive Detection of Copper(II) in Aqueous Solution.

Project description:The development of chemosensors able to detect analytes in a variety of sample matrices through a low-cost, fast, and direct approach is of current interest in food, health, industrial, and environmental fields. This contribution presents a simple approach for the selective and sensitive detection of Cu2+ ions in aqueous solution based on a transmetalation process of a fluorescent substituted Zn(salmal) complex. Transmetalation is accompanied by relevant optical absorption changes and quenching of the fluorescence emission, leading to high selectivity and sensitivity of the chemosensor, with the advantage of not requiring any sample pretreatment or pH adjustment. Competitive experiments demonstrate a high selectivity of the chemosensor towards Cu2+ with respect to the most common metal cations as potential interferents. A limit of detection down to 0.20 μM and a dynamic linear range up to 40 μM are achieved from fluorometric data. By exploiting the fluorescence quenching upon formation of the copper(II) complex, simple paper-based sensor strips, visible to naked eyes under UV light, are used for the rapid, qualitative, and quantitative in situ detection of Cu2+ ions in aqueous solution over a wide concentration range, up to 10.0 mM, in specific environments, such as in industrial wastewater, where higher concentrations of Cu2+ ions can occur.

| S-EPMC10141078 | biostudies-literature

Selective Adsorption of Sr(II) from Aqueous Solution by Na3FePO4CO3: Experimental and DFT Studies

Project description: Not available

| S-EPMC11206743 | biostudies-literature

Expanding Glycomic Investigations through Thiol-Derivatized Glycans.

Project description:N-(2-thioethyl)-2-aminobenzamide (TEAB), a novel glycan auxiliary, was synthesized and its utility was evaluated. The auxiliary was conjugated to glycans by reductive amination with the water-stable reagent 2-picoline borane complex. Glycan products, which ranged from 1 to 7 linked hexoses, were all isolated in yields ranging from 60% to 90% after purification by reverse-phase chromatography. The novel conjugate introduces a convenient, shelf-stable thiol directly onto the desired free glycans with purification advantages and direct modification with efficient reactions through alkenes, halides, epoxides, disulfides, and carboxylates in yields of 49% to 93%. Subsequently, a thiol-selective modification of the BSA protein was used to generate a neoglycoprotein with a bifunctional PEG-maleimide linker. To further illustrate the utility of a thiol motif, 2-thiopyridine activation of a thiol-containing support facilitated the covalent chromatographic purification of labeled glycans in yields up to 63%. Finally, initial proof of concept of implementation in a light printed microarray was explored and validated through FITC-labeled concanavalin A binding. In conclusion, the thiol-functionalized glycans produced greatly expand the diversity of bioconjugation tools that can be developed with glycans and enable a variety of biological investigations.

| S-EPMC9964202 | biostudies-literature

Facile Synthesis of Thiol-Functionalized Magnetic Activated Carbon and Application for the Removal of Mercury(II) from Aqueous Solution.

Project description:To improve the adsorption capacity, reduce the disposal cost, and enhance the separation efficiency of common activated carbon as an adsorbent in wastewater treatment, a novel thiol-modified magnetic activated carbon adsorbent of NiFe2O4-PAC-SH was successfully synthesized with a facile and safe hydrothermal method without any toxic and harmful reaction media. The as-prepared NiFe2O4-PAC-SH can effectively remove mercury(II) ions from aqueous solution. The maximal adsorption capacities from the experiment and Langmuir fitting achieve 298.8 and 366.3 mg/g at pH 7, respectively, exceeding most of adsorptive materials. The as-prepared NiFe2O4-PAC-SH has an outstanding regeneration performance, remarkable hydrothermal stability, and efficient separation efficiency. The data of kinetics, isotherms, and thermodynamics show that the adsorption of mercury(II) ions is spontaneous and exothermic. Ion exchange and electrostatic attraction are the main adsorption factors. The experimental results exhibit that the NiFe2O4-PAC-SH can be a prominent substitute for conventional activated carbon as an adsorbent.

| S-EPMC6648564 | biostudies-literature

Complexation between the Antioxidant Pterostilbene and Derivatized Cyclodextrins in the Solid State and in Aqueous Solution.

Project description:Inadequate aqueous solubilities of bioactive compounds hinder their ability to be developed for medicinal applications. The potent antioxidant pterostilbene (PTB) is a case in point. The aim of this study was to use a series of modified water-soluble cyclodextrins (CDs), namely, hydroxypropyl β-CD (HPβCD), dimethylated β-CD (DIMEB), randomly methylated β-CD (RAMEB), and sulfobutyl ether β-CD sodium salt (SBECD) to prepare inclusion complexes of PTB via various solid, semi-solid, and solution-based treatments. Putative CD-PTB products generated by solid-state co-grinding, kneading, irradiation with microwaves, and the evaporative treatment of CD-PTB solutions were considered to have potential for future applications. Primary analytical methods for examining CD-PTB products included differential scanning calorimetry and Fourier transform infrared spectroscopy to detect the occurrence of binary complex formation. Phase solubility analysis was used to probe CD-PTB complexation in an aqueous solution. Complexation was evident in both the solid-state and in solution. Complex association constants (K1:1) in an aqueous solution spanned the approximate range of 15,000 to 55,000 M-1; the values increased with the CDs in the order HPβCD < DIMEB < RAMEB < SBECD. Significant PTB solubility enhancement factors were recorded at 100 mM CD concentrations, the most accurately determined values being in the range 700-fold to 1250-fold.

| S-EPMC9966925 | biostudies-literature

Silica encapsulation of thiol-stabilized lead selenide (PbSe) quantum dots in aqueous solution.

Project description:Silica encapsulation of lead selenide quantum dots (PbSe QDs) in aqueous solution is reported. Thioglycolic acid (TGA) stabilized PbSe QDs were modified with 3-mercaptopropyl trimethoxysilane (MPS) through vigorous stirring in water for 18-24 h in alkaline solution (pH 10.4-10.6). Silica shell was developed by controlled deposition and precipitation of silicates from sodium silicate solution onto MPS modified QDs surfaces. TEM images showed multiple PbSe QDs encapsulated in silica shell. The size of PbSe-SiO2 core-shell nanocrystals was estimated to be 25-30 nm by TEM. Elemental compositions (Pb, Se and Si) were investigated by EDX analysis. The purified colloids of PbSe-SiO2 QDs were stable for months when kept at 4 °C.

| S-EPMC3665949 | biostudies-literature

Synthesis of a novel hexaazatriphenylene derivative for the selective detection of copper ions in aqueous solution.

Project description:A hexaazatriphenylene (HAT) derivative, naphtho[2,3-h]naphtho[2',3':7,8]quinoxalino[2,3-a]naphtho[2',3':7,8]quinoxalino[2,3-c]phenazine-5,10,15,20,25,30-hexaone (NQH) was synthesized, characterized, and found to have novel properties in being selective toward the detection of copper (Cu2+) ions. The capability of NQH to be employed as a colorimetric, chemo-fluorescence and electrochemical sensor for the detection of Cu2+ was demonstrated by performing UV-Vis absorbance, fluorescence intensity, and cyclic voltammetry (CV) measurements. The interaction between NQH and Cu2+ was initially observed with an obvious color change from yellow to brown upon the addition of Cu2+ ions to NQH. The interaction was also confirmed by UV-Vis absorbance, fluorescence intensity, and mass spectroscopy (MS/MS) measurements. UV absorbance, fluorescence and CV of NQH toward Cu2+ showed good linearity with a detection limit of 3.32 μM, 2.20 μM and 0.78 μM, respectively, which are lower than the toxicity levels of copper in drinking water (20-30 μM) set by the U.S. Environmental Protection Agency (EPA) and World Health Organization (WHO). A 1 : 2 stoichiometry complexation between NQH and Cu2+ was confirmed by Job's plot and MS/MS. In addition, the selectivity and sensitivity of the NQH compound towards Cu2+ ions were further confirmed by performing CV on a screen printed flexible and planar electrochemical sensor.

| S-EPMC9076171 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data