A Novel Hg<Superscript>2+</Superscript> Selective Ratiometric Fluorescent Chemodosimeter Based on an Intramolecular FRET Mechanism

A irreversible Hg²⁺ selective ratiometric fluorescence probe FR, a fluorescein fluorophore linked to a rhodamine B hydrazide by a thiourea spacer, was designed and synthesized. The developed probe FR exhibited great ratiometric fluorescence enhancement and remarkable yellow-magenta color change toward Hg²⁺ with excellent selectivity in aqueous acetone solution, and the ratiometric fluorescence response to Hg²⁺ was not interfered by other metal cations including Fe³⁺, Co²⁺, Ni²⁺, Cr³⁺, Zn²⁺, Pb²⁺, Cd²⁺, Ca²⁺, Mg²⁺, Ba²⁺ and Mn²⁺. The linear range and the detection limit of this supposed ratiometric fluorescence method for Hg²⁺ were 0.0–10.0 × 10⁻⁶ and 5 × 10⁻⁸ M, respectively.     

An NBD-based Sensitive and Selective Fluorescent Sensor for Copper(II) Ion

A new 7-nitrobenz-2-oxa-1,3-diazole (NBD) derived fluorescent probe (1) exhibiting high selectivity for Cu²⁺ detection, produced significant fluorescence quenching in the presence of Cu²⁺ ion, while the metal ions Ca²⁺, Cd²⁺, Co²⁺, Fe²⁺, Hg²⁺, Mg²⁺, Mn²⁺, Ni²⁺ and Zn²⁺ produced only minor changes in fluorescence. The apparent association constant (K _a) for Cu²⁺ binding in chemosensor 1 was found to be 1.22 × 10³ M⁻¹. The maximum fluorescence quenching activity caused by Cu²⁺ binding to 1 was observed over the pH range 6–10.     

Studies on Interaction of Norfloxacin,Cu<Superscript>2+</Superscript>, and DNA by Spectral Methods

The interactions of norfloxacin (NFA), DNA, and Cu²⁺ are studied by fluorescence and UV-spectra method. According to the experimental results, it can be concluded that NFA can form a steady binary complex with Cu²⁺. There is a linear relationship between the Fluorescence intensity of the norfloxacin–Cu²⁺–DNA system and the concentration of DNA. And when the concentration of the NFA is 1.95×10⁻⁵ mol L⁻¹, they possess a good linearity in the concentration of DNA ranged from 4.7×10⁻⁶ to 2.8×10⁻⁵ mol L⁻¹.It is a good method due to the high sensitivity and selectivity.     

A Coumarin-Based Fluorescent Chemosensor for Zn<Superscript>2+</Superscript> in Aqueous Ethanol Media

A coumarin-based fluorescent chemosensor 1 for Zn²⁺ was designed and synthesized. Compound 1 exhibits lower background fluorescence due to intramolecular photoinduced electron transfer. However, upon mixing with Zn²⁺ in 30% (v/v) aqueous ethanol, a “turn-on” fluorescence emission is observed. The fluorescence emission increases linearly with Zn²⁺ concentration in the range 0.5–10 μmol L⁻¹ with a detection limit of 0.29 μmol L⁻¹. No remarkable emission enhancement was, however, observed for other metal ions. The proposed chemosensor was applied to the determination of Zn²⁺ in water samples with satisfactory results.     

Study on the New Fluorescence Enhancement System of Tb –N-(2 - Pyridinyl) Ketoacetamide-Et<Subscript>3</Subscript>N-Zn and its Application

A sensitive fluorescence enhancement system was developed for the determination of zinc (II). The fluorescence intensity of the Tb- N- (2 - Pyridinyl) ketoacetamide (PKA) system was greatly enhanced by the addition of triethylamine (Et₃N) and zinc nitrate in the methanol solution. The excitation and emission wavelengths were 329 nm and 546 nm, respectively. Under optimal conditions, the fluorescence intensities varied linearly with the concentration of Zn²⁺ in the range of 8.0×10⁻⁷−5.0×10⁻⁶ M with a detection limit of 9.9×10⁻⁸ M. The interferences of some substances were described. This method was applied to the determination of amounts of Zn²⁺ in soybean, rice, and wheat, respectively. The results showed that the proposed procedure is a high selective, simple, and rapid method to the determination of Zn²⁺ ion. The mechanism of fluorescence enhancement was also studied.     

Spectroscopic Studies of a New Multi-Element Sensitive Fluorescent Probe Derived from 2-(2-pyridyl)benzimidazole: Selective Discrimination of Zn2+ from Its Congeners

ABSTRACT

A new multielement sensitive fluorescent probe, 1-(2-(phenylthio)ethyl)-2-(pyridin-2-yl)-1H-benzo[d]imidazole (L), has been synthesized by the reaction between 2-(pyridyl) benzimidazole and 2-chloroethyl phenyl sulfide. Excitation and emission wavelength of L are at 330 and 371 nm, respectively. Among various transition and nontransition metal ions, it can selectively read Zn²⁺ ion as the emission wavelength of L undergoes a red shift by 31 nm upon binding with Zn²⁺ in methanol. In the presence of Cd²⁺, Hg²⁺, and other common cations, the emission wavelength of L remains unchanged, and thus allows us to discriminate Zn²⁺ from its congeners. Both L and its Zn²⁺ complex are well characterized by different spectroscopic techniques like ¹H-NMR, ESI-TOF (+) mass, FT-IR, and elemental analysis data. The binding constant value of the complexation reaction between L and Zn²⁺ is found as 724.6 M^?1 in methanol. Density functional theoretical (DFT) studies nicely demonstrate the red shift in the emission wavelength of L upon binding with Zn^2+.     

Design and Synthesis of Highly Photostable Yellow–Green Emitting 1,8-Naphthalimides as Fluorescent Sensors for Metal Cations and Protons

Two highly photostable yellow–green emitting 1,8-naphthalimides 5 and 6, containing both N-linked hindered amine moiety and a secondary or tertiary cation receptor, were synthesized for the first time. Novel compounds were configured as “fluorophore–spacer–receptor” systems based on photoinduced electron transfer. Photophysical characteristics of the dyes were investigated in DMF and water/DMF (4:1, v/v) solution. The ability of the new compounds to detect cations was evaluated by the changes in their fluorescence intensity in the presence of metal ions (Cu²⁺, Pb²⁺, Zn²⁺, Ni²⁺, Co²⁺) and protons. The presence of metal ions and protons was found to disallow a photoinduced electron transfer leading to an enhancement in the dye fluorescence intensity. Compound 5, containing secondary amine receptor, displayed a good sensor activity towards metal ions and protons. However the sensor activity of dye 6, containing a tertiary amine receptor and a shorter hydrocarbon spacer, was substantially higher. The results obtained indicate the potential of the novel compounds as highly photostable and efficient “off–on” pH switchers and fluorescent detectors for metal ions with pronounced selectivity towards Cu²⁺ ions.     

A New Sensitive and Selective Off-On Fluorescent Zn<Superscript>2+</Superscript> Chemosensor Based on 3,3′,5,5′-Tetraphenylsubstituted Dipyrromethene

3,3′,5,5′-Tetraphenyl-2,2′-dipyrromethene was described as a highly sensitive and selective Off-on fluorescent colorimetric chemosensor for Zn²⁺ based on the chelation-enhanced fluorescence (CHEF) effect. The reaction of dipyrromethene ligand with Zn²⁺ induces the formation of the [ZnL₂] complex, which exhibits the increasing fluorescence in 120 fold compared with ligand in the propanol-1/cyclohexane (1:30) binary mixture. The Zn²⁺ detection limit was 1.4 × 10^?7 М. The UV-Vis and fluorescence spectroscopic studies demonstrated that the dipyrromethene sensor was highly selective toward Zn²⁺ cations over other metal ions (Na⁺, Mg²⁺, Co²⁺, Ni²⁺, Fe³⁺, Cu²⁺, Mn²⁺, Cd²⁺ and Pb²⁺), excluding Hg²⁺.     

A New Fluorescent Chemosensor Detecting Co<Superscript>2+</Superscript> and K<Superscript>+</Superscript> in DMF Buffered Solution

A new fluorescent chemosensor 2-(2-thiophene)imidazo [4,5,f]-1,10-phenanthroline (L) was prepared and characterized. By adding univalent or divalent metal ions such as Na⁺, K⁺, Mg²⁺, Ba²⁺, Mn²⁺, Fe²⁺, Co²⁺, Ni²⁺, Cu²⁺, Ag⁺, Zn²⁺, Cd²⁺ and Hg²⁺ ions into the solution of L in DMF under buffered conditions with the working pH ranging from 7.0 to 8.0, we found that L could be used to detect K⁺ ratiometricly and it could also be applied to sense Co²⁺ with the phenomenon of fluorescence quenching of L. While the response behavior of L was not discernibly affected by other examined metal ions.