Co-II,(III), Ni-II, and Cu-II complexes of new dehydroacetic acid N4-substituted thiosemicarbazones have been studied. The substituted thiosemicarbazones, N4-dimethyl-(DA4DM), N4-diethyl-(DA4DE), 3-piperidyl-(DApip) and 3-hexamethyleneiminyl-( DAhexim), when reacted with the metal chlorides, produced two Co-II complexes, [Co(DA4DE)Cl-2] and [Co(DAhexim)(2)Cl-2]; two Co-III complexes, [Co(DA4DM-H)(2)Cl] and [Co(DApip-H)(DA-pip2H)]; a paramagnetic Ni-II complex, [Ni(DAhexim)(DAhexim-H)Cl]; three diamagnetic Ni-II complexes, [Ni(DA4DM-H)Cl], [Ni(DA4DE-H)Cl] and [Ni(DApip-H)Cl]; and four Cu-II complexes with the analogous stoichiometry of the latter three Ni-II complexes. These new thiosemicarbazones have been characterized by their melting points, as well as i.r., electronic and H-1- n. m. r. spectra. The metal complexes have been characterized by i.r. and electronic spectra, and when possible, n. m. r. and e.s.r. spectra, as well as elemental analyses, molar conductivities, and magnetic susceptibilities. The crystal and molecular structure of the four-coordinate Cu-II complex, [Cu(DAhexim-H)Cl] has been determined by single crystal X-ray diffraction and the anionic ligand coordinates via an oxygen of the dehydroacetic acid and the thiosemicarbazone moiety's imine nitrogen and thione sulfur.