Enhancement of CsNO3 extraction 1,2-dichloroethane by tris(2-aminoethyl)amine triamide derivatives via a dual-host strategy
Article
Kavallieratos, K, Danby, A, Van Berkel, GJ et al. (2000). Enhancement of CsNO3 extraction 1,2-dichloroethane by tris(2-aminoethyl)amine triamide derivatives via a dual-host strategy
. ANALYTICAL CHEMISTRY, 72(21), 5258-5264. 10.1021/ac0005971
Kavallieratos, K, Danby, A, Van Berkel, GJ et al. (2000). Enhancement of CsNO3 extraction 1,2-dichloroethane by tris(2-aminoethyl)amine triamide derivatives via a dual-host strategy
. ANALYTICAL CHEMISTRY, 72(21), 5258-5264. 10.1021/ac0005971
A systematic study of a dual-host system exhibiting pairwise anion/cation separations has been performed for CsNO3 extraction. Tripodal triamides 1-4 and 9 derived from condensation of hexanoic (for 1), octanoic (for 2), decanoic (for 3), lauric (for 4), and p-tert-butylbenzoic (for 9) acid with tris(2-aminoethyl)amine (tren) were used together with tetrabenzo-24-crown-8, a well-known Cs+ cation receptor. By using 5 mM crown ether in the organic phase and 10 mM CsNO3 with 0.1 mM HNO3 in the aqueous phase, tripods 1, 2, and 9 enhance CsNO3 extraction by factors of 2.4, 1.7, and 4.4, respectively (for 50 mM amide concentration), while the corresponding monoamide controls 5-8 derived from n-propylamine (5, 6) or N,N'-dimethylethylenediamine (7, 8) and hexanoic (5, 7) or octanoic (6, 8) acid derivatives gave no significant enhancement under the same conditions. This behavior may be ascribed to nitrate complexation by the triamides, which lowers the overall thermodynamic barrier for the salt transfer to the organic phase. The nitrate binding was confirmed by 1H NMR titration of receptor solutions, using tetrabutylammonium nitrate. Association constants for the formation of the anion-nitrate complexes were found to vary between 33 and 52 M-1 for the more soluble triamides. The synergistic effects for CsNO3 extraction are in reasonable agreement with the values predicted theoretically from the measured association constants. Electrospray ionization mass spectrometry confirmed the predominant formation of 1:1 tripod-nitrate complexes. Monoamide controls gave no evidence of anion complexation.
