Abstract
The present study includes the synthesis of phthalocyanine compounds with general formula X4PcM where M= Fe (III) and Fe (II), X is a peripheral substitution in the position-4 on the four benzene rings which include NO2, NH2 and Schiff base (p-imino phenyl amine). The proposed main compound is tetra-diiminobenzene-p-aminobenzene phthalocyaninato metal. Two kinds of peripheral substitution of phthalocyanine compounds were synthesized, first are planner the other is bridged. The structures of the synthesized compounds were confirmed by elemental analysis, UV-visible, IR and X-ray diffraction techniques. The elemental analysis results showed a good agreement with the theoretical results. The absorption spectra for all compounds showed the characteristic phthalocyanine bands (Q and B bands). In general, the two bands show a clear blue shift for Schiff base phthalocyanine compounds in comparison with the tetra amino phthalocyanine. The infra-red spectra of all compounds were recorded and the spectra of tetraamines derivatives showed two weak bands attributed to the NH2 groups at the range 3245-3330 cm-1 and 3190-3240 cm-1 which are attributed to asymmetric and symmetric stretching vibration respectively. The IR-spectra of Schiff-base compounds show a strong band at the range 1600-1608cm-1 corresponding to the C=N stretching vibrations. X-ray diffraction gives the d-spacing (interplanner spacing) of the planes of the crystalline regions which are regarded as the fingerprints for the compounds. In addition, they can be used to calculate the states around Fermi levels during the calculation of α which is regarded as the inverse of the interplanner spacing.
Keywords
Phthalocyanine
Schiff base
tetra-diiminobenzene-p-aminobenzene phthalocyanines
X-Ray diffraction.