An all-solid-state monohydrogen phosphate sensor based on a macrocyclic ionophore.

An all-solid-state electrode, containing a synthesized chiral A(2)B(2) macrocyclic compound namely (4R,5R,15R,16R)-4,5,15,16-tetraphenyl-3,6,14,17-tetraazatricyclo [13.3.1.18,12] tetracosa-1(23),8,10,12(24)19,21-hexaene-2,7,13,18-tetrone as an ionophore in polyvinyl chloride (PVC)/polyurethane (PU) membrane matrix, has been developed for the selective quantification of monohydrogen phosphate ions. The best performing membrane contained PVC, PU, ionophore, and nitrophenyl octyl ether as a plasticizer in the ratio 32.2:2.6:65.1 (w/w, %). It exhibited a near-Nernstian slope of 31.0+/-1.0 mV/decade of activity for HPO(4)(2-) ions in the concentration range of 1. 10(-6) to 1.0 x 10(-2)M at pH 7.4. The detection limit of the electrode was 8.4 x 10(-7)M and the life time was six weeks. The electrode displayed excellent selectivity for monohydrogen phosphate over other anions and the selectivity sequence was determined as HPO(4)(2-)>SO(4)(2-)>Ac(-)>NO(3)(-)>ClO(4)(-)>Cl(-)>I(-). The selective electrode for the monohydrogen phosphate ions was evaluated with a standard reference material (SRM 1548) and the titration of the sample solution.