Synthesis, electrochemical, in situ spectroelectrochemical and in situ electrocolorimetric characterization of new metal-free and metallophthalocyanines substituted with 4-{2-[2-(1-naphthyloxy)ethoxy]ethoxy} groups

• Published in: Polyhedron Vol. 29; no. 5; pp. 1475 - 1484
• Main Authors: Acar, Irfan, Bıyıklıoğlu, Zekeriya, Koca, Atıf, Kantekin, Halit
• Format: Journal Article
• Language: English
• Published: OXFORD Elsevier Ltd 30.03.2010; Elsevier
• Subjects: Chemistry; Chemistry, Inorganic & Nuclear; Chromaticity diagram; Crystallography; Cyclic voltammetry; Phthalocyanine; Phthalonitrile; Physical Sciences; Science & Technology; Spectroelectrochemistry; Synthesis; Cyclic voltammetry; Phthalocyanine; Phthalonitrile; Synthesis; Chromaticity diagram; Spectroelectrochemistry; ZN(II); COPPER; PHTHALOCYANINES; GAS SENSORS; COBALT
• ISSN: 0277-5387
• DOI: 10.1016/j.poly.2010.01.032

The synthesis of novel metal-free and metallophthalocyanines [Ni(II), Zn(II), Co(II), Cu(II)] were prepared by cyclotetramerization of a novel 4-{2-[2-(1-naphthyloxy)ethoxy]ethoxy}phthalonitrile and the corresponding metal salts (NiCl 2, Zn(CH 3COO) 2, CoCl 2 and CuCl 2). The structures of the target compounds were confirmed using elemental analysis, IR, 1H NMR, 13C NMR, UV–Vis and MS spectral data. Voltammetric and in situ spectroelectrochemical measurements show that while cobalt phthalocyanine complex gives both metal-based and ring-based redox processes, metal-free, and zinc phthalocyanines show only ring-based reduction and oxidation processes. All complexes decomposed and coated on the electrode as nonconductive film at positive potential window of the electrolyte. An in situ electrocolorimetric method has been applied to investigate color of the electro-generated anionic and cationic forms of the complexes. The synthesis of novel metal-free and metallophthalocyanines [Ni(II), Zn(II), Co(II), Cu(II)] were prepared by cyclotetramerization of a novel 4-{2-[2-(1-naphthyloxy)ethoxy]ethoxy}phthalonitrile and the corresponding metal salts (NiCl 2, Zn(CH 3COO) 2, CoCl 2 and CuCl 2). The structures of the target compounds were confirmed using elemental analysis, IR, 1H NMR, 13C NMR, UV–Vis and MS spectral data. Voltammetric and in situ spectroelectrochemical measurements show that while cobalt phthalocyanine complex gives both metal-based and ring-based redox processes, metal-free, and zinc phthalocyanines show only ring-based reduction and oxidation processes. All complexes decomposed and coated on the electrode as nonconductive film at positive potential window of the electrolyte. An in situ electrocolorimetric method has been applied to investigate color of the electro-generated anionic and cationic forms of the complexes.