Somayeh Heydari

A thermodynamic study of complex formation between dicyclohexyl-18-crown-6 (DCH18C6) and La3+, UO22+, Ag+, and NH4+ cations in acetonitrile-tetrahydrofuran binary media using conductometric method

The complex formation between La3+, UO22+ Ag+, and NH4+ cations and macrocyclic ligand, dicyclohexyl-18-crown-6 (DCH18C6), was studied in acetonitrile-tetrahydrofuran (AN-THF) binary mixtures at different temperatures using the conductometric method. The results show that with the exception of complexation of the NH4+ cation with DCH18C6 in pure acetonitrile, the stoichiometry of all the complexes is being 1: 1 (M: L). The stability constants of the complexes were determined using a GENPLOT computer program. The nonlinear behavior which was observed for changes of log Kf of the complexes versus the composition of the mixed solvent was discussed in terms of solvent-solvent interaction in their binary solution, which results in 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 of DCH18C6 for the studied cations changes with the composition of the AN-THF binary system. The sequence of stabilities of complexes in an AN-THF binary solution (mol. % AN = 75.0) at 25°C is [(DCH18C6)La)]3+ > [(DCH18C6)UO2]2+ > [(DCH18C6)Ag]+ ∼ [(DCH18C6)NH4]+, but in the case of other binary systems of AN/THF (mol. % AN = 25.0 and 50.0) is [(DCH18C6)La]+ > [(DCH18C6)NH4]+ ∼ [DCH18C6)UO2]2+ > [(DCH18C6)Ag]+.

Electrochemical behavior of para-nitroaniline at a new synthetic crown ether-silver nanoparticle modified carbon paste electrode

A new synthetic ligand (6,7,9,10,17,18,19,20,21,22-decahydrodibenzo[h,r][1,4,7,11,15] trioxadiazacyclonanodecine-16,23-dione, DTD)–Ag nanoparticles (AgNP) modified carbon paste electrode (DTD/Ag–CPE) is fabricated. Voltammetric behavior and determination of para-nitroaniline (PNA) is explored. The influence of various experimental parameters on the electrode response is investigated. Under optimized conditions the peak current showed a good linear relationship with p-nitroaniline concentration in the range 1 × 10−6 mol L−1 to 1 × 10−4 mol L−1. The proposed electrode was applied to p-nitroaniline determination in water samples.