Journal of Porphyrins and Phthalocyanines, cilt.14, sa.3, ss.227-234, 2010 (SCI-Expanded)
The reactions of unsymmetrical porphyrins (1 and 2) with Ni(OAc) 2· 4H2O in boiling DMF produce porphyrin complexes (3 and 4). From the reactions of free porphyrin ligands 1 and 2 with hexachlorocyclotriphosphazatriene, N3P3Cl6, the new free porphyrino-phosphazene derivatives (5 and 6) are obtained. On the other hand, the reactions of N3P3Cl6 with porphyrin complexes (3 and 4) afford the new porphyrino-phosphazene complexes (7 and 8). In the literature there are a few examples of the porphyrino- phosphazene architectures. The structural investigations of all the compounds have been made by elemental analyses, MS, FTIR, 1H NMR, 31P NMR and UV-visible techniques. The cyclic voltammograms (CVs) are examined in acetonitrile (MeCN) containing 0.1 M tetrabutylammonium- tetrafluoroborate (TBATFB) to investigate the surface attachment properties at the glassy carbon electrode (GCE) and the influence of the presence of metal cations in the porphyrin ring. © 2010 World Scientific Publishing Company.