New Benzo-15-Crown-5 Ethers Featuring Salicylic Schiff Base Substitutions – Synthesis, Complexes and Structural Study

Abstract

Condensation reactions between 4'-formyl-5'-hydroxybenzo-15-crown-5and 2-aminopyridine, 2-amino-6-methylpyridine, 2-amino-4-methylpyridine or2-(aminomethyl)furan yielded the new laterally functionalized crown ethers1–4. The crown compounds 1–3 form crystalline 1:1 (Na+:ligand) complexes 1a–3a with sodium perchlorate. Ligands and complexes have been characterized by elemental analyses, IR, UV-Vis, 1H-, 13C-NMR and mass spectra. The tautomeric equilibria (phenol-imine, O...H–N and keto-amine, O...H–N forms) have been systematically studied by using UV-Vis absorption spectra. The spectra of the ligands 1–4 and complexes 1a–3a were recorded in polar, non-polar, acidic, and basic media. In solutions of polar solvents, tautomeric interconversion of the Schiff base into the keto-amine form has been observed. A crystal structure [monoclinic, space group P21/c,a = 14.292(2), b = 9.449(6), c = 16.059(2) A, β = 114.20(1)°,V = 1978.4(13) A3, Z = 4 and Dx = 1.314 g cm-3] shows that compound 4 is in the form of phenol-imine in solid state. There is a strong intramolecular [O–H...N 1.78(6), O...N 2.581(7), O–H 0.89(6) A and N...H–O 148.4(5)°] hydrogen bond between the phenolic oxygen and imine nitrogen atoms. The C=N imine bond reveals a trans planar (1E) configuration. The molecules stack in columns parallel to the a/c plane of the unit cell.