The present report describes two series of new porphyrazine macrocycles derived from tetrakis(selenodiazole)porphyrazine, TSeDPzH(2), having the formulae [TSeDPzM](CH3COOH)(H2O)(x) M = Mn(II), Co(II), Ni(II), Zn(II); x = 4-6) and [TSeDPzM(py)](CH3COOH)(H2O), (M = Mn(II), Co(II), Ni(II); x = 1-5), obtained by reaction of the free ligand with the appropriate metal acetate in dimethyl (DMSO), and, respectively, pyridine. All the species isolated are stable-to-air substantially amorphous materials, almost completely insoluble in the usual organic solvents and N-donors(pyridine etc.), and only slightly soluble in CF3COOH or 96% H2SO4. The complexes have been investigated by IR, Raman, and UV-vis spectra. and magnetic susceptibility measurements. Their properties in terms of electronic structure and reactivity towards N-bases are discussed in comparison with their S-containing analogs and the class of the structurally similar metal phthalocyanines.
Tetrakis(selenodiazole) porphyrazines. 2: Metal complexes with Mn(II), Co(II), Ni(II), and Zn(II)
E M Bauer;
2001
Abstract
The present report describes two series of new porphyrazine macrocycles derived from tetrakis(selenodiazole)porphyrazine, TSeDPzH(2), having the formulae [TSeDPzM](CH3COOH)(H2O)(x) M = Mn(II), Co(II), Ni(II), Zn(II); x = 4-6) and [TSeDPzM(py)](CH3COOH)(H2O), (M = Mn(II), Co(II), Ni(II); x = 1-5), obtained by reaction of the free ligand with the appropriate metal acetate in dimethyl (DMSO), and, respectively, pyridine. All the species isolated are stable-to-air substantially amorphous materials, almost completely insoluble in the usual organic solvents and N-donors(pyridine etc.), and only slightly soluble in CF3COOH or 96% H2SO4. The complexes have been investigated by IR, Raman, and UV-vis spectra. and magnetic susceptibility measurements. Their properties in terms of electronic structure and reactivity towards N-bases are discussed in comparison with their S-containing analogs and the class of the structurally similar metal phthalocyanines.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
