Compound 1 has been prepared by the reaction of 4-nitrophthalonitrile and trans-2-methoxy-4-(2-nitrovinil)phenol by the common method of nucleophilic substitution of an activated nitro group in an aromatic ring. The metallophthalocyanines 2, 3 were prepared by the reaction of a dinitrile derivative with Co(OAc)(2) or Zn(OAc)(2) in DMSO. The lutetium bis-(phthalocyaninato) complex 4 was obtained by treating the dinitrile derivative with lutetium acetate and DBU in 1-hexanol. The new compounds were characterized by elemental analyses, FT-IR, (1)H-NMR, MALDI-TOF MS and UV/Vis spectral data. The spectroscopic data of the new compounds were in accordance with the structures. The temperature and frequency dependence of dielectric and conduction properties of the spin coated film of compounds (2-4) have been studied by fabricating metal-Pc-metal structures. The results show that compound 2 has giant dielectric constant. At a low range of frequency and room temperature, ε' is found to be equal to 2.33 × 10(6), 1.53 × 10(4) and 1.03 × 10(4) for 2, 3 and 4, respectively. The giant dielectric behavior of 2 is mainly attributed to Maxwell-Wagner polarization. The obtained results also indicated that the frequency dependence of the dielectric permittivity, ε'(ω), exhibits non-Debye type relaxation for all temperatures investigated. The ac conductivity results gave a temperature dependent frequency exponent s. The results were compared with the prediction of the Quantum Mechanical Tunneling and Correlated Barrier Hopping models.
In this study, 4-hydroxysalicylaldehyde-p-aminoacetophenoneoxime (LH) was synthesized starting from p-aminoacetophenoneoxime and 4-hydroxysalicylaldehyde. Complexes of this ligand with Co(II), Ni(II), Cu(II) and Zn(II) were prepared with a metal : ligand ratio of 1 : 2. The ligand and its metal complexes have been characterized by elemental analyses, IR, 1 H-and 13 C-NMR spectra, magnetic susceptibility measurements and thermogravimetric analyses (TGA).
Metal phthalocyanines containing an unsymmetrically substituted nitro group were synthesized from 4-nitrophthalonitrile and the corresponding anhydrous metal salts ( Co ( OAc )2, Zn ( OAc )2) by the method of statistically mixed condensation reactions. The new type of metallo-bisphthalocyanine compounds connected by a N = N bridge was prepared from the reactions of respective nitro compounds with sodium hydroxide ( NaOH ) and activated zinc powder in a mixture of methanol ( MeOH ) and tetrahydrofuran (THF). The structures of these compounds were characterized by using 1 H NMR, IR, elemental analyses, UV-vis and magnetic circular dichroism spectroscopies.
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