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An efficient and concise approach for the synthesis of 2,4,6-triphenyl pyridines has been developed through copper-catalyzed oxidative decarboxylation coupling of C(sp3) aryl acetic acids with oxime acetates in DMF at...

The acid-base equilibrium of 1,10-phenanthroline (1,10-phen) in the presence of polyethylene glycol 400 (PEG-400, non-ionic) and tetrabutylammonium bromide (TBAB, ionic) micellar media has been studied by Calvin-Wilson titration technique at different mole fractions (0.5%-2.5%) of PEG-400 and TBAB micellar solutions at an ionic strength of 0.16 mol dm −3 NaCl and at a temperature of 298 K. The pH metric data were subjected to SCPHD program to obtain correction factor and K w which were given as initial inputs for MINIQUAD75 program to refine protonation constants. HySS program was then used to generate the species distribution diagrams versus pH using the results obtained from the MINIQUAD75 program and SIM run data. The difference in values of protonation constants in aqueous medium (logβ 1 = 4.93 & logβ 2 = 6.22) and in the micellar media (PEG-400, logβ 1 = 4.89 & logβ 2 = 5.91 and TBAB, logβ 1 = 4.84 & logβ 2 = 5.73) is attributed to different intrinsic solvent characteristics of micelles. In case of ionic surfactants, the electrostatic micellar surface is an additional contributing factor.

Protonation constants of a viral inhibitor, aurintricarboxylic acid were determined using potentiometric method of data acquisition followed by chemometric modelling methods of analysis in the presence of two different kinds of micellar media, CTAB, a cationic micelle and SDS, an anionic micelle. MINIQUAD75 program was used for the determination of the plausible species and their corresponding formation constants at 303 ± 0.1 K and 0.01 M ionic strength. Five formation constants were identified corresponding to five ionizable hydrogens. Species concentration distribution diagrams were generated using Origin software. Best-fit chemical models were selected on the basis of statistical parameters like standard deviation (SD), U (sum of the squares of the residuals in mass balance equations) and chi-square test. It was found that the formation constants are lower in CTAB micellar medium while there is no significant change in the presence of SDS compared to aqueous medium.

A new preconcentration method which utilises a mixture of cationic and anionic surfactants for separation and spectrophotometric determination of iron and cobalt simultaneously has been developed. The metal ions, iron and cobalt were complexed with thiocyante. The hydrophobic complexes of iron and cobalt were then extracted into catanionic mixed micelles of cetyltrimethylammonium bromide (CTAB) and sodium dodecyl sulphate (SDS). Different parameters like concentration of HCl, concentration of thiocyanate, concentrations of the surfactants (CTAB and SDS), equilibration temperature and time were studied to get maximum efficiency. The linear ranges of Fe3+ and Co2+ were found to be 0.139 – 0.838 μg mL–1 and 5.89 – 35.4 μg mL–1, respectively the detection limits obtained were 1.54 ng mL–1 and 6.18 ng mL–1. The developed procedure has been employed for the retrieval of Fe3+ and Co2+ in water samples successfully (tap water and sea water). 98 – 107% recoveries were obtained.