Abstract
The synthesis of air-sensitive 2, 6-diformyl-4-tert-butylthiophenol dioxime H3L3 was achieved by a Pd-mediated S–C cleavage of the corresponding S-tert-butyl protected thioether. The novel ligand forms a dinuclear, neutral PdII2 complex, which is stabilized by two N···HO hydrogen bonds to give a pseudo-macrocyclic structure. The crystal structure of a PdII complex of an oxidized isothiazole derivative of H3L3 is also reported.
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