Tetrakis(4-N,N-dimethylaminobenzene)porphyrinato]manganese(III) acetate as a novel carrier for a selective iodide PVC membrane electrode.

[5,10,15,20-Tetrakis(4-N,N-dimethylaminobenzene)porphyrinato]Mn(III) acetate (MnTDPAc) was applied as an ionophore for an iodide-selective PVC membrane electrode. The influences of the membrane composition, pH of the test solution and foreign ions on the electrode performance were investigated. The sensor exhibited not only excellent selectivity to iodide ion compared to Cl- and lipophilic anions such as ClO4- and salicylate, but also a Nernstian response with a slope of -59.4 +/- 1.2 mV per decade for iodide ions over a wide concentration range from 1.0 x 10(-2) to 7.5 x 10(-6) M at 25 degrees C. The potentiometric response was independent of the pH of the solution in the pH range of 2 - 8. The electrode could be used for at least 2 months without any considerable divergence in the potential. Good selectivity for iodide ion, a very short response time, simple preparation and relatively long-term stability were the silent characteristics of this electrode. It was successfully used as an indicator electrode in the potentiometric titration of iodide ions, and also in the determination of iodide from seawater samples and drug formulations.     

Kinetic study of the oxidation of ethanol by 3,4-lutidine chromium(VI) peroxide in dichloromethane solution

The oxidation kinetics of ethanol with 3,4-lutindine chromium(VI) peroxide (LCP) were investigated by monitoring the absorbance change at 565 nm in dichloromethane solution. The reaction had a first-order dependence on oxidant and a fractional (one half) dependence on reactant. The stoichiometric ratio between LCP and ethanol was 1 : 2. The activation parameters were determined from temperature dependence of the reaction rate. It was found that the cleavage of the peroxide groups of LCP is primarily responsible for the oxidant of ethanol to acetaldehyde. Based on the kinetic results obtained (including deuterium isotope effect) a plausible mechanism is proposed. © 1994 John Wiley & Sons, Inc.     

Specific Uphill Transport of Zinc as Zn(SCN)42− Ion using Na+-Dicyclohexyl-18-Crown-6 as Carrier

Sodium-dicyclohexyl- 18-crown-6 complex cation was used as carrier for the uphill transport of zinc as Zn(SCN)₄^2? complex anion. By using L-cysteine as a metal ion acceptor in the receiving phase at the optimized pH of 7.6, the amount of zinc transport through the liquid membrane after 90 min was 97.2 ± 1.0%. The selectivity and efficiency of zinc transport from aqueous solutions containing equimolar mixtures of Ag⁺, Cd²⁺ Co²⁺, Cu²⁺, Fe²⁺, Ni²⁺, Pb²⁺, Pd²⁺, Sr²⁺, Bi³⁺, Cr³⁺ and Fe³⁺ ions was investigated. In the presence of NH₂OH.HCl as a suitable masking agent in the source phase, the interfering effect of Cu²⁺ and Pb²⁺ ions was diminished drastically.     

Spectrophotometric study of interaction of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone with diaza-18-crown-6 and diaza-15-crown-5 in acetonitrile and chloroform solutions

Interactions of diaza-18-crown-6 and diaza-15-crown-5, as electron donors, with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), as an electron acceptor, have been investigated spectrophotometrically in acetonitrile and chloroform solutions. The results indicated immediate formation of an electron donor-electron acceptor complex DA: [reaction in text] which is followed by two relatively slow consecutive reactions: [reaction in text]. The pseudo-first-order rate constants for the formation of the ionic intermediate and the final product have been evaluated at various temperatures by computer fitting of the absorbance time data to appropriate equations. The formation constants of the resulting DA complexes have also been determined. The influences of both the azacrown's structure and the solvent properties on the formation of DA complexes and the rates of subsequent reactions are discussed.     

A study of peroxyoxalate-chemiluminescence of acriflavine

The chemiluminescence arising from the reaction of bis(2,4,6-trichlorophenyl)oxalate (TCPO) with hydrogen peroxide in the presence of acriflavine has been studied. The relationship between the chemiluminescence intensity and concentrations of TCPO, H2O2, acriflavine and the base sodium salicylate are reported. The kinetic parameters for the peroxyoxalate-chemiluminescence (PO-CL) of acriflavine were evaluated from the computer fitting of the corresponding chemiluminescence intensity-time plots.     

NMR Study of the Stoichiometry, Stability, and Ligand Interchange of Silver Ion-Hexathia-18-crown-6 Complex in Binary Dimethyl Sulfoxide Solvent Mixtures at 300 K

Proton NMR was used to study the complexation reaction between silver ion and hexathia-18-crown-6 in a number of binary mixed solvents of dimethyl sulfoxide with acetonitrile and methanol. Formation constants for the resulting 1:1 complexes in different solvent mixtures were determined by computer fitting of the chemical shift-mole ratio data. The influence of solvent composition on the stability of the resulting complex is discussed. The exchange kinetics of Ag⁺-hexathia-18-crown-6 in 70-30 wt.% dimethyl sulfoxide-acetonitrile and 75-25 wt.% dimethyl sulfoxide-methanol were studied by proton NMR line-shape analysis. In both solvent mixtures, the exchange of thiacrown ether between the free and complexed sites was found to proceed via a dissociative pathway. The exchange rates and the activation parameters E _a, H , S, and G for the ligand exchange were determined and the influence of solvent properties on these parameters discussed.     

Conductance study of ammonium complexes with several crown ethers and cryptands in nitrobenzene,acetonitrile and dimethylformamide solutions

The formation of ammonium complexes with several crown ethers and cryptands in nitrobenzene, acetonitrile and dimethylformamide solutions was investigated by conductometry at 25°C. Stability constants of the resulting 1:1 complexes sere determined from the molar conductance-mole ratio data and found to vary in the order DC18C6>18C6>DB30C10>DB21C7>DB24C8>DB18C6>15C5>B15C5>12C4, in the case of crown complexes, and in the order C222>C221>C211>C22>C21 for the ammonium cryptates. The stabilities of the complexes varied inversely with the Gutmann donicity of the solvents. Influences of the number of members in the macrocycle, nature of the substituents in the polyether ring, cavity size and dimensionality, conformations of the free and complexed ligands and number of N⁺–H bonds available for hydrogen bonding are discussed.     

Nanocrystalline TiO2-HClO4:A novel,efficient and recyclable catalyst for the chemoselective N-Boc protection of amines under solvent-free conditions

Nanocrystalline TiO₂-HClO₄,as newly reported catalyst,has been used as an efficient and reusable catalyst for the chemoselective N-Boc protection of amines.The clean,mild acidity condition, quantitative yields of products,short reaction time and low reaction temperature are attractive features of this reaction.In practice,this method is a combination of a satisfactory synthesis and more significantly easy product isolation and purification.     

Preparation of Silica-Bonded S-Sulfonic Acid: A Recyclable Catalyst for the Synthesis of Bis-Indolylmethanes

Silica bonded S-sulfonic acid (SBSSA) was prepared by the reaction of 3-mercaptopropylsilica (MPS) and chlorosulfonic acid in chloroform. Silica-bonded S-sulfonic acid, as a reusable solid acid catalyst, was used for the condensation reactions of indole with carbonyl compounds at ambient temperature. Tetra-(indolyl)methanes were also obtained by the condensation reaction of indole with dialdehyde compounds. Silica bonded S-sulfonic acid was recovered and reused.

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