Abstract

The possibility was demonstrated to use metal coordination for the resolution of racemic chiral N-thiophosphorylated thioureas through controlling the stereochemistry of the complex formation and supramolecular chiral recognition during crystallization. A series of new Ni(II) complexes derived from chiral N-thiophosphorylated thioureas with 1,3-N,S-coordination were synthesized in enantiopure and racemic forms and characterized by X-ray single crystal diffraction. It was shown that square-planar centrosymmetric nickel ion coordination results in exclusive formation of meso-complexes from racemic ligands. The symmetry break of the nickel ion coordination by the introduction of pyridine co-ligand into the apical position promotes chiral recognition of the ligands upon complexation with formation of exclusively homochiral complexes. Further supramolecular recognition might be achieved by variation of crystal growth conditions, with racemic crystals being obtained at higher initial concentrations, including t...

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