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1.
Lei Qian  Xiurong Yang 《Talanta》2007,73(1):189-193
In this paper, we demonstrate an electrochemiluminescence (ECL) enhancement of tris(2,2-bipyridyl)ruthenium(II) (Ru(bpy)32+) by the addition of silver(I) ions. The maximum enhancement factor of about 5 was obtained on a glassy carbon electrode in the absence of co-reactant. The enhancement of ECL intensity was possibly attributed to the unique catalytic activity of Ag+ for reactions between Ru(bpy)33+ with OH. The higher enhancement was observed in phosphate buffer solutions compared with that from borate buffer solutions. This resulted from the fact that formation of nanoparticles with large surface area in the phosphate buffer solution exhibited high catalytic activity. The amount of Ag+, solution pH and working electrode materials played important roles for the ECL enhancement. We also studied the effects of Ag+ on Ru(bpy)32+/tripropylamine and Ru(bpy)32+/C2O42− ECL systems.  相似文献   

2.
The complexation reactions between Mg2+,Ca2+,Sr2+ and Ba2+ metal cations with macrocyclic ligand, dicyclohexano-18-crown-6 (DCH18C6) were studied in methanol (MeOH)–water (H2O) binary mixtures at different temperatures using conductometric method . In all cases, DCH18C6 forms 1:1 complexes with these metal cations. The values of stability constants of complexes which were obtained from conductometric data show that the stability of complexes is affected by the nature and composition of the mixed solvents. While the variation of stability constants of DCH18C6-Sr 2+ and DCH18C6-Ba2+versus the composition of MeOH–H2O mixed solvents is monotonic, an anomalous behavior was observed for variations of stability constants of DCH18C6-Mg2+ and DCH18C6-Ca2+ versus the composition of the mixed solvents. The values of thermodynamic parameters (ΔHc°, ΔSc°) for complexation reactions were obtained from temperature dependence of formation constants of complexes using the van’t Hoff plots. The results show that in most cases, the complexation reactions are enthalpy stabilized but entropy destabilized and the values of thermodynamic parameters are influenced by the nature and composition of the mixed solvents. The obtained results show that the order of selectivity of DCH18C6 ligand for metal cations in different concentrations of methanol in MeOH–H2O binary system is: Ba2+>Sr2+>Ca2+> Mg2+.  相似文献   

3.
Various methods of synthesizing functional derivatives of dithia-13(16)-crown-4(5) ethers are proposed. Complex-formation of the obtained compounds with Ag+ and Pb2+ ions has been studied using 1H NMR. A radiometric method was used to investigate the extracting ability of substituted dithia-13(16)-crown-4(5) ethers in relation to Ag+ and Cd2+ ions from aqueous solution in the presence of anions of various degree of hardness, with determination of the metal content. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 233–243, February, 2006.  相似文献   

4.
The complexation reactions between Ag+, Hg2+ and Pb2+ metal cations with aza-18-crown-6 (A18C6) were studied in dimethylsulfoxide (DMSO)–water (H2O) binary mixtures at different temperatures using the conductometric method. The conductance data show that the stoichiometry of the complexes in most cases is 1:1(ML), but in some cases 1:2 (ML2) complexes are formed in solutions. A non-linear behaviour was observed for the variation of log K f of the complexes vs. the composition of the binary mixed solvents. Selectivity of A18C6 for Ag+, Hg2+ and Pb2+ cations is sensitive to the solvent composition and in some cases and in certain compositions of the mixed solvent systems, the selectivity order is changed. The values of thermodynamic parameters (ΔH co, ΔS co) for formation of A18C6–Ag+, A18C6–Hg2+ and A18C6–Pb2+ complexes in DMSO–H2O binary systems were obtained from temperature dependence of stability constants and the results show that the thermodynamics of complexation reactions is affected by the nature and composition of the mixed solvents.  相似文献   

5.
Azo 8-hydroxyquinoline benzoate (2) was synthesized and studied to detect metal ions. Distinct color change was found for compound 2 in the presence of transition metal ions Hg2+ or Cu2+ in CH3CN, respectively, which makes it possible for distinguishing Hg2+ and Cu2+ from other metal ions by the ‘naked eye’.  相似文献   

6.
The complexation reactions between Mg2+, Ca2+, Sr2+ and Ba2+ cations with the macrocyclic ligand, 18-Crown-6 (l8C6) in water–methanol (MeOH) binary systems as well as the complexation reactions between Ca2+ and Sr2+ cations with 18C6 in water–ethanol (EtOH) binary mixtures have been studied at different temperatures using conductometric method. The conductance data show that the stoichiometry of all the complexes is 1:1. It was found that the stability of 18C6 complexes with Mg2+, Ca2+, Sr2+ and Ba2+ cations is sensitive to solvent composition and in all cases, a non-linear behaviour was observed for the variation of log K f of the complexes versus the composition of the mixed solvents. In some cases, the stability order is changed with changing the composition of the mixed solvents. The selectivity order of 18C6 for the metal cations in pure methanol is: Ba2+ > Sr2+ > Ca2+ > Mg2+. The values of thermodynamic parameters (Δ H c ° and Δ S c °) for formation of 18C6–Mg2+, 18C6–Ca2+, 18C6–Sr2+ and 18C6–Ba2+complexes were obtained from temperature dependence of the stability constants. The obtained results show that the values of (Δ H c ° and Δ S c °) for formation of these complexes are quite sensitive to the nature and composition of the mixed solvent, but they do not vary monotonically with the solvent composition.This revised version was published online in July 2005 with a corrected issue number.  相似文献   

7.
García CD  Ortiz PI 《Talanta》2003,61(4):547-556
Four routes for the modification of carbon electrodes with humic acids and the determination of three divalent metallic cations were studied. The determination of bound Fe2+, Cu2+ and Ni2+ was performed by cyclic and square wave voltammetry using either a batch or flow analysis system. Using the FIA system and SWV, linear relationships between the oxidation (or reduction) current and the cations concentration were obtained with the modified electrodes, while no signals were obtained for the same conditions for bare carbon electrodes. The system can be used to study the interaction between a wide range of electroactive cations and humic substances; however, the performance as an analytical tool is limited due to the high limits of detection (μM). However, some advantages like simplicity, short analysis time, inexpensive instrumentation needs and miniaturization capabilities are remarkable.  相似文献   

8.
The structural and dynamical properties of high-spin Ru2+ in aqueous solution have been theoretically studied using molecular dynamics (MD) simulations. The conventional MD simulation based on pair potentials gives the overestimated average first shell coordination number of 9, whereas the value of 5.9 was observed when the three-body corrected function was included. A combined ab initio quantum mechanical/molecular mechanical (QM/MM) molecular dynamics simulation has been performed to take into account the many-body effects on the hydration shell structure of Ru2+. The most important region, the first hydration shell, was treated by ab initio quantum mechanics at UHF level using the SBKJC VDZ ECP basis set for Ru2+ and the 6-31G basis sets for water. An exact coordination number of 6 for the first hydration shell was obtained from the QM/MM simulation. The QM/MM simulation predicts the average Ru2+–O distance of 2.42 Å for the first hydration shell, whereas the values of 2.34 and 2.46 Å are resulted from the pair potentials without and with the three-body corrected simulations, respectively. Several other structural properties representing position and orientation of the solvate molecules were evaluated for describing the hydration shell structure of the Ru2+ ion in dilute aqueous solution. A mean residence time of 7.1 ps was obtained for water ligands residing in the second hydration shell.  相似文献   

9.
Non-linear absorption spectral data obtained from ternary mixtures of analytes are analyzed by using a linear model, iterative target transformation factor analysis (ITTFA). The use of transformed original variables is used to correct non-linearities in the original data. Absorbance below a certain limit (k) is described as linear and above this limit as non-linear. The extension of the regressor variables is the squared absorbances above the linear range. The variation of the prediction error as a function of the number of the factors and the k-values were considered and the minimum prediction error was evaluated for reaching to optimum. Except the natural non-negativity constraint the correlation constraint also is used on concentration vector in each iteration of ITTFA algorithm. The reliability of the method is evaluated using model data for ternary mixtures by spectral overlapping and different degrees of non-linearity. Simultaneous spectrophotometric determination of Eu3+, UO22+ and Th4+ with arsenazo III as chromogenic reagent is used as experimental model systems with non-linearity behavior of Eu3+and UO22+ components. The application to both synthetic and real data sets with different degrees of non-linearity demonstrate the ability of the proposed methodology to obtain better results than original data and ITTFA. The relative standard errors of prediction for proposed method in comparison with using the PLS calibration on original and extended data are nearly smaller.  相似文献   

10.
A series of competitive metal ion transport experiments have been performed. Each involved transport from an aqueous source phase across an organic membrane phase into an aqueous receiving phase. The source phase contained equimolar concentrations of cobalt(II), nickel(II), cupper(II), zinc(II), cadmium(II), silver(I) and lead(II) metal cations. The membrane phase incorporated ionophore, decyl-18-crown-6. The membrane solvents include: chloroform, dichloromethane, 1,2-dichloroethane, nitrobenzene and chloroform–nitrobenzene binary solvents. A good transport efficiency and selectivity of Pb2+ transport from aqueous solutions are observed in this investigation. The selectivity order for competitive bulk liquid membrane transport of the studied transition and post transition metal cations through chloroform is: Pb2+>Co2+>Ni2+>Ag+>Cd2+, but in the case of dichloromethane, 1,2-dichloroethane and nitrobenzene as liquid membranes, the selectivity sequences were found to be: Pb2+>Co2+>Cd2+>Cu2+>Ag+>Ni2+>Zn2+, Pb2+>Co2+>Ag+>Ni2+>Zn2+ and Pb2+>Co2+>Ni2+>Zn2+>Cd2+>Ag+, respectively. The transport rate of the metal cations in chloroform–nitrobenzene binary solvents is sensitive to the solvent composition. The transport processes were studied in absence and presence of the stearic acid and the results show that the sequence of selectivities and ion transport rates change in the presence of stearic acid.  相似文献   

11.
Introduction: Safranal, which endows saffron its unique aroma, causes vasodilatation and has a hypotensive effect in animal studies, but the mechanisms of these effects are unknown. In this study, we investigated the mechanisms of safranal vasodilation. Methods: Isolated rat endothelium-intact or -denuded aortic rings were precontracted with phenylephrine and then relaxed with safranal. To further assess the involvement of nitric oxide, prostaglandins, guanylate cyclase, and phospholipase A2 in safranal-induced vasodilation, aortic rings were preincubated with L-NAME, indomethacin, methylene blue, or quinacrine, respectively, then precontracted with phenylephrine, and safranal concentration–response curves were established. To explore the effects of safranal on Ca2+ influx, phenylephrine and CaCl2 concentration–response curves were established in the presence of safranal. Furthermore, the effect of safranal on aortic rings in the presence of ouabain, a Na+-K+ ATPase inhibitor, was studied to explore the contribution of Na+/Ca2+ exchanger to this vasodilation. Results: Safranal caused vasodilation in endothelium-intact and endothelium-denuded aortic rings. The vasodilation was not eliminated by pretreatment with L-NAME, indomethacin, methylene blue, or quinacrine, indicating the lack of a role for NO/cGMP. Safranal significantly inhibited the maximum contractions induced by phenylephrine, or by CaCl2 in Ca2+-free depolarizing buffer. Safranal also relaxed contractions induced by ouabain, but pretreatment with safranal totally abolished the development of ouabain contractions. Discussion/Conclusion: Inhibition of Na+-K+ ATPase by ouabain leads to the accumulation of Na+ intracellularly, forcing the Na+/Ca2+ exchanger to work in reverse mode, thus causing a contraction. Inhibition of the development of this contraction by preincubation with safranal indicates that safranal inhibited the Na+/Ca2+ exchanger. We conclude that safranal vasodilation is mediated by the inhibition of calcium influx from extracellular space through L-type Ca2+ channels and by the inhibition of the Na+/Ca2+ exchanger.  相似文献   

12.
A novel single-armed Salamo-type bisoximes (H4L) has been designed and synthesised. An obvious colour change from yellow (H4L) to pale pink (HL-Pb2+) which can be visually observed by the naked eye in visible light. H4L can act as a fluorescent sensor for ratiometric recognition of Zn2+ with high selectivity and sensitivity. Crystallographic data of the [Cu(HL)(μ-OAc)Cu] reveals that the two Cu2+ ions are both penta-coordinated with square pyramidal geometries, and forms a 2D supramolecular plane structure by hydrogen bonding interactions.  相似文献   

13.
Graphene quantum dots (GQDs), inheriting the superb property of graphene oxide, possess smaller lateral size and high biocompatibility, thus having potential in biomedical applications. We previously discovered that GQDs, combining with Cu2+ ions, could cleave DNA primarily through an oxidative pathway; yet, oxidative DNA cleavage is not practically preferred in biology. In this work, we explore the DNA cleavage ability of GQDs with Zn2+ and Ni2+. Zn2+ and Ni2+ alone are incapable of cleaving supercoiled DNA, but when combining with the GQDs, Zn2+ and Ni2+ exhibit DNA cleavage activity. However, the activity of these two systems is much lower than that of GQDs/Cu2+, and GQDs/Ni2+ is less active than GQDs/Zn2+. The functional mechanism of GQDs/Ni2+ and GQDs/Zn2+ is different from that of GQDs/Cu2+. The GQDs play a key role in the two systems; the redox inactive Zn2+ and Ni2+ ions assist to generate the oxidative species that eventually lead to the DNA cleavage. The current results together with our previous result indicate that GQDs together with metal ions can cleave supercoiled DNA, and their cleavage activities depend on the properties of metal ions: for redox active metal ions, metal ions play key roles, for redox inactive metal ions, GQDs are dominant.  相似文献   

14.
The complex formation between Cu2+, Zn2+, Tl+ and Cd2+ metal cations with macrocyclic ligand, dibenzo- 18-crown-6 (DB18C6) was studied in dimethylsulfoxide (DMSO)–ethylacetate (EtOAc) binary systems at different temperatures using conductometric method. In all cases, DB18C6 forms 1:1 complexes with these metal cations. The stability constants of the complexes were obtained from fitting of molar conductivity curves using a computer program, Genplot. The non-linear behaviour which was observed for variations of log K f of the complexes versus the composition of the mixed solvent was discussed in terms of changing the chemical and physical properties of the constituent solvents when they mix with one another and, therefore, changing the solvation capacities of the metal cations, crown ether molecules and even the resulting complexes with changing the mixed solvent composition. The results show that the selectivity order of DB18C6 for the metal cations in pure ethylacetate and pure dimethylsulfoxide is: Tl+ > Cu2+ > Zn2+ > Cd2+ but the selectivity order is changed with the composition of the mixed solvents. The values of enthalpy changes (ΔH°C) for complexation reactions were obtained from the slope of the van’t Hoff plots and the changes in standard enthalpy (ΔS°C) were calculated from the relationship: ΔG°C,298.15H°C − 298.15 ΔS°C. The obtained results show that in most cases, the complexes are enthalpy stabilized, but entropy destabilized and the values of ΔH°C and ΔS°C depend strongly on the nature of the medium.  相似文献   

15.
合成了2,4-二(2-噻吩乙烯基)-6-(4'-N,N-二甲氨基苯乙烯基)-1,3,5-均三嗪(2)并鉴定了其结构。在乙腈-水混合介质中,化合物2在355和416nm处呈现双吸收峰,加入Cu2+,Hg2+ 和Fe3+ 后,均在520nm附近形成新的吸收峰。化合物2与Cu2+、Hg2+ 和Fe3+ 均形成1:1型配合物,其结合常数分别为1.9×105L·mol-1,6.6×103L·mol-1,2.7×103L·mol-1。对照化合物4与金属离子的光谱响应与化合物2相似,仅吸收峰的位置不同。因此,可认为化合物24中三嗪环中的N和噻吩环中的S与Cu2+、Hg2+ 和Fe3+ 共同配位形成了稳定的金属配合物。  相似文献   

16.
近年来,水溶性聚磷酸铵在液体肥料和复合肥料的领域受到了广泛的关注,并在发达国家中得到了大面积的推广及应用。在pH值为5.5~8.0、温度为278.15 K~323.15 K的条件下,本文采用滴定法研究Ca2+-Mg2+-Zn2+体系在聚磷酸铵溶液中的螯合规律。实验结果表明:相同质量分数的聚磷酸铵溶液对金属离子的螯合量会随着体系中Ca2+、Mg2+、Zn2+的摩尔浓度的变化而变化;随着温度的升高而逐渐降低;随着pH的增加而逐渐增加;随着聚合度的升高而逐渐增加。采用傅里叶红外光谱对聚磷酸铵和A1B3C3体系的螯合物进行表征。  相似文献   

17.
In this work, we synthesised and characterised three novel fluorescence macrocyclic sensors containing optically active dansyl groups. The studies for the interaction of the synthesised compounds with various mental ions (Li+, Na+, K+, Ag+, Mg2+, Ca2+, Ba2+, Pb2+, Zn2+, Co2+, Cd2+, Hg2+, Ni2+, Cu2+, Mn2+, Cr3+, Al3+, Fe3+) were performed by fluorescence titration, Job’s plot, ESI-MS and DFT calculations. The results showed that the sensors 1a–1c displayed selective recognition for Cu2+ and Fe3+ ions and formed stoichiometry 1:1 complex through PET mechanism in DMSO/H2O solution (1:1, v/v, pH 7.4 of HEPES). The binding constant (K) and detection limit were calculated.  相似文献   

18.
The transport experiments of Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Ag+ and Pb2+ metal cations were carried out by dibenzo-18-crown-6 (DB18C6), dibenzyl-diaza-18-crown-6 (Dibenzyl-diaza-18C6) and di-tert-butyl-dibenzo-18-crown-6 (Di-tert-butyl-DB18C6) using chloroform (CHCl3), 1,2-dichloroethane (1,2-DCE) and nitrobenzene (NB) organic solvents as liquid membranes. The source phase contained equimolar concentration of these metal cations and the source and receiving phases being buffered at pH=5 and pH=3, respectively. The obtained results show that the selectivity and the efficiency of transport for these heavy metal cations change with the nature of the ligand and also the organic solvents, which were used as liquid membranes in these experiments. A good selectivity was observed for silver (I) ion by dibenzyl-diaza-18C6 in all membrane systems. Dibenzo-18C6 and di-tert-butyl-DB18C6 showed the highest transport efficiency for cobalt (II) ion. The effect of stearic acid on transport efficiency was also investigated and the results show that the efficiency of transport of the heavy metal cations increases in the presence of this organic acid.  相似文献   

19.
Simultaneous spectrophotometric methods are described for the determination of Zn2+, Co2+ and Ni2+ by 1-(2-pyridylazo)2-naphthol (PAN) in micellar media, using absorbance correction-H-point standard addition method (HPSAM) and partial least squares (PLS) regression. The ligand and its metal complexes, i.e. Zn2+-PAN, Co2+-PAN and Ni2+-PAN, were made water-soluble by the neutral surfactant Triton X-100, and therefore extraction with organic solvents was no longer required. Formation of all of these complexes was complete within 10min at pH 9.2. The linear range was 0.1–1.5mgL–1 for Zn2+, 0.1–2.0mgL–1 for Co2+ and 0.1–2.0mgL–1 for Ni2+. The relative standard deviation (RSD) for the simultaneous determination of 0.50mgL–1 each of Zn2+, Ni2+ and Co2+ by applying the H-point standard addition method was 2.55%, 2.04% and 3.70%, respectively. The total relative standard error for applying the PLS method to 9 synthetic samples in the linear ranges of these metals was 1.8%. Interference effects of common anions and cations were studied, and both methods were applied to the simultaneous determination of Zn2+, Co2+ and Ni2+ in alloy samples.  相似文献   

20.
Silica gels doped with Cu2+ ions were prepared from the (3-aminopropyl) trimethoxysilane (APTMOS)/tetraethoxysilane (TEOS) systems. Sols showed a broad absorption peak at 640 nm, suggesting 3–5 coordination of the aminopropyl groups to Cu2+. For gels prepared from APTMOS and dried at room temperature, the 640 nm peak decreased and a red-shifted absorption appeared below 400 nm within a few months. The luminescence spectra of the xerogels showed emission bands at 430–470 and 510 nm. The former and latter bands are ascribed to Cu+ monomer and dimer emissions, respectively. These results indicate that Cu2+ ions are reduced to Cu+. When xerogels were prepared from APTMOS/TEOS = 1 (vol/vol), the color of xerogels was blue with an absorption peak at around 670 nm, indicating no reduction of Cu2+ ions.  相似文献   

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