2-Azahetaryl-2-(oxoindolin-2-ylidene)acetonitriles as Colorimetric Probes for Zn: Synthesis and Optical Properties

[Image: see text] A new one-pot approach for the synthesis of the Zn(2+)-sensitive probes 2-azahetaryl-2-(oxoindolin-2-ylidene)acetonitriles 3a–c and 4 is described. The method includes the in situ formation of imidoylchloride and its further condensation with azahetarylacetonitrile 1. The structure of the obtained compounds is studied using (1)H nuclear magnetic resonance (NMR), (13)C NMR, infrared (IR), high-resolution mass spectrometry (HRMS), and UV–Vis spectroscopy techniques. Two model ligands both exhibiting the highest extinction coefficient and the best solubility in a Tris buffer pH 7.2/dimethyl sulfoxide (DMSO) solution, namely 5-methyl-benzothiazole derivative 3b and benzoxazole derivative 4, are thoroughly studied as colorimetric probes for Zn(2+). The probe 3b has the highest sensitivity to Zn(2+), showing a limit of ion detection (LOD) calculated by the 3S criterion of 0.43 μM and selectivity upon masking Cu(2+) ions with Na(2)S(2)O(3). The composition of the complexes in the solution was determined by the limited logarithm method. The stability constant (lg K) values of 3b-Zn of 10.27 ± 0.02 and 4-Zn of 12.5 ± 0.2 indicate the formation of complexes of average stability.