Abstract:
Tetrasubstituted metal-free {2H[Pc(S(CH(2))(6)OCOC(4)H(3)S)(4)]} and copperphthalocyanine {Cu[Pc(S(CH(2))(6)OCOC(4)H(3)S)(4)]}, bearing thiophene-2-carboxylate-hexylthio moieties, have been prepared as isomeric mixtures via cyclo-tetramerization. Both new compounds have been characterized by elemental analysis, FTIR, (1)H and (13)C NMR, MS (Maldi-TOF) and UV-Vis spectral data, The cation binding abilities of the functional phthalocyanines with Ag(I), Pd(II), Hg(II), Pb(II) and Cd(II) are evaluated by a monomer-oligomer formation technique with U-V-Vis spectroscopy. Spectroscopic properties of the complexes were affected strongly by the electron-donating sulfanyl units on the periphery. Cyclic voltammetry and differential pulse voltammetry studies show that both compounds give up to three ligand based reduction processes and one ligand-based oxidation process having diffusion-controlled one electron transfer properties. (C) 2007 Elsevier Ltd. All rights reserved.