Design and synthesis of new chemosensors for fluoride anion (F-)1-6 have been of interest to chemists for many years, because F- plays a crucial role in the dental care5 and the treatment of osteoporosis7. Recently, the fluorescent chemosensors of fluorid… 相似文献
We report the synthesis of two new anion receptors of a covalently linked 1,3,5-triarylbenzoamido-crown ether. Our results show that combined with a picrate salt they act by means of an intermolecular charge transfer process (EDA complex), as naked-eye sensors for basic anions, especially for sodium phytate in DMSO/H2O (1:1). 相似文献
A novel chemosensor, namely 3‐(4‐chlorophenyl)‐1‐(pyridin‐2‐yl)prop‐2‐en‐1‐one, CPPEO, and its metal complexes have been synthesized and characterized by using sets of chemical and spectroscopic techniques, such as elemental analysis, mass, Fourier transform‐infrared and UV–Vis spectral analysis. The thermal properties of the metal complexes have been investigated by thermogravimetric techniques. The decomposition mechanism of the titled complexes was suggested. The results showed that the Co2+ and Mn2+ complexes have an octahedral geometry, while Zn2+ and Cd2+ complexes have tetrahedral geometry. The kinetic and thermodynamic parameters of the thermal decomposition stages have been evaluated using the Coats–Redfern method. The optical sensing response of the investigated chemosensor to the different metal ions was investigated. It responds well to the tested metal ions as reflected from the significant change in both absorption and emission spectra upon adding different concentrations of the metal salts, confirming the intramolecular charge transfer of the chemosensor upon effective coordination with the used metal ions. This leads to enhancing ICT interaction, causing a significant shift in the presence of strongly complexing metal ions. This was fully reversible, where the solution of dye‐metal ion complex was decomplexed by adding an EDTA solution to revert the original spectrum of the dye. The stability constants, K, for the complexes of the investigated chemosensor with the mentioned metal ions were calculated, indicating that Co2+ is the most effectively detected, and the potential of the novel dye was highly efficient switchers for Co2+ ions. Additionally, the molecular modeling was carried out for the chemosensor and its metal complexes. Finally, the solid complexes have been tested for their in vitro antimicrobial activities against some bacterial strains (Gram +ve and Gram ?ve bacteria), as well as antifungal strains. 相似文献
Two novel lactam-containing compounds based on simple naphthodipyrrolidones have been developed as colorimetric sensors for fluoride anion with high selectivity and sensitivity. The two compounds can selectively act with fluoride anion and exhibit the naked-eye visible color change from purple to blue, and the detection limit could reach the concentration as low as 3.0 × 10?6 M. The proton nuclear magnetic resonance titrations reveal the happen of intermolecular proton transfer between the hydrogen atom on the lactam N and the fluoride anion. Quantum chemical calculations indicate that the deprotonation can alleviate the distorted degree between the peripheral phenyl and the naphthodipyrrolidone core, and raise the frontier molecular orbital energy levels and decrease the band gap, rendering the protonated molecules a new more batho-chromic absorption band. 相似文献
A series of polymer chemosensors containing naphthalimide signal moiety and imide recognition moiety for the selective detection of fluoride ions (F−) were synthesized by reversible addition‐fragmentation chain transfer (RAFT) polymerization. The polymer chemosensors display obvious absorption and fluorescence variations upon the addition of F−, which can be observed by both naked eyes and optical responses. The polymers showed higher fluorescence enhancement than its monomer, and the polymers with higher molecular weight have higher sensitivity than those with lower molecular weight. Other halide anions are found to hardly induce any variation of either the absorption or fluorescence spectra.
Anion receptors employing two distinct sensory mechanisms are rare. Herein, we report the first examples of halogen-bonding porphyrin BODIPY [2]rotaxanes capable of both fluorescent and redox electrochemical sensing of anions. 1H NMR, UV/visible and electrochemical studies revealed rotaxane axle triazole group coordination to the zinc(II) metalloporphyrin-containing macrocycle component, serves to preorganise the rotaxane binding cavity and dramatically enhances anion binding affinities. Mechanically bonded, integrated-axle BODIPY and macrocycle strapped metalloporphyrin motifs enable the anion recognition event to be sensed by the significant quenching of the BODIPY fluorophore and cathodic perturbations of the metalloporphyrin P/P+. redox couple. 相似文献
A novel dimeric calixpyrrole has been synthesized. The dimer forms stable complexes with p-nitrophenolate ion with a concomitant reduction in extinction coefficient. The chromogenic anion is displaced by the addition of various anions like fluoride and acetate. Effective optical sensing of these anions is accomplished using the calixpyrrole dimer. 相似文献
There is a large interest in luminescent materials for application as temperature sensors. In this scenario, we investigate the performance of neodymium-doped alkaline-earth fluoride (Nd3+:MF2; M=Ba, Ca, Sr) crystalline powders prepared by combustion synthesis for optical temperature-sensing applications based on the luminescence intensity ratio (LIR) technique. We observe that the near-infrared luminescence spectral profile of Nd3+ changes with the temperature in a way that its behavior is suitable for optical thermometry operation within the first biological window. We also observe that the thermometric sensitivities of all studied samples change depending on the spectral integration range used in the LIR analysis. Nd3+:CaF2 presents the largest sensitivity values, with a maximum absolute sensitivity of 6.5×10−3/K at 824 K and a relative sensitivity of 1.71 %/K at human-body temperature (310 K). The performance of CaF2 for optical thermometry is superior to that of β-NaYF4, a standard material commonly used for optical bioimaging and temperature sensing, and on par with the most efficient oxide nanostructured materials. The use of thermometry data to help understand structural properties via Judd-Ofelt intensity standard parameters is also discussed. 相似文献
Novel calixsalen-type cavitands have been synthesized using metal-free synthesis from simple and inexpensive materials, such as ethylenediamine and 5,5′-methylene-bis-salicylaldehyde derivatives. The cavitand 1 containing salen functionality recognizes fluoride ion. Fluoride ions switch on fluorescence on binding with the cavitand 1. Substitution on bis-salicylaldehyde part of calixsalen-type cavitand shows change in recognition behavior. On the attachment of electron withdrawing substituent, such as nitro group, the cavitand lost its fluorescence properties but proved to be a better colorimetric probe showing marked color change from pale yellow to red on addition of tetrabutyl ammonium salt of fluoride ion to the solution of cavitand. The nitro substituted cavitand is highly sensitive and selective for fluoride anion and hence is a promising candidate for development of colorimetric chemosensor. The binding of the cavitands with fluoride ion is investigated using 1H NMR-titration experiments. 相似文献
Novel fluorescent chemosensor with good selectivity for F? anion was designed and synthesized. The sensor has a bearing on a single functionalized pillar[5]arene and Fe3+ metal complex (PN‐Fe), which showed prominent fluorescent response for F? anion over other common anions (Cl?, Br?, I?, AcO?, HSO4?, H2PO4?, ClO4?, CN? and SCN?). These results were evaluated by fluorescent method. The detection limit of PN‐Fe to F? was calculated to be 2.50×10?7 mol/L. Moreover, the sensor PN‐Fe3+ might serve as a recyclable component in sensing materials. 相似文献
A novel azoimine dye-based colorimetric chemosensor (1) has been designed and synthesised for dual recognition of copper(II) and fluoride ions in aqueous media. Significantly, the outstanding dual-ion recognition properties along with the excellent reversibility prompted us to consider 1 as an ideal candidate for fabrication of multiple logic circuits. According to the response profile of 1 towards Cu2+ and F? inputs, we developed a unique tunable system integrated with one INHIBIT logic gate as well as one OR gate. Also, 1 behaved as a molecular keypad lock with sequential addition of Cu2+ and F? inputs. In accession, a reversible ‘Write–Read–Erase–Read’ function with complementary ‘IMP/INH’ logic gate has been demonstrated through a feedback loop using F? and trifluoroacetic acid as two chemical inputs. To the best of our knowledge, this is the first report where the symmetrical bis azo-azomethine dye has been exploited as a molecular keypad lock. 相似文献
A new fluorescent chemosensor based on bithiophene coupled dimesitylborane (BMB-1) was synthesized and characterized. BMB-1 was used for colorimetric and turn-on fluorescent sensing of cyanide (CN−) and fluoride (F−) ions, in the presence of other competitive anions in an aqueous (CH3CN–H2O) medium. BMB-1 showed a hypsochromic shift (blue shift) with addition of CN− and F− ions in absorption studies. The lower detection level of CN− and F− ions is 1.37 × 10−9 and 1.75 × 10−9 M, respectively. The BMB-1 binding mechanism is based on the nucleophilic addition of CN− and F− ions in the internal charge transfer transition of bithio moiety to the boranylmesitylene unit, and the color changes were observed under UV light. This result is further confirmed by Fourier transform infrared spectroscopy, mass spectrometry and density functional theory calculations. Also, the BMB-1 probe is found to be a good adsorbent for the removal of F− ions in real water samples using the adsorption technique. 相似文献