Synthesis, electrochemical, in situ spectroelectrochemical and in situ electrocolorimetric characterization of new phthalocyanines peripherally fused to four flexible crown ether moieties

被引:33
作者
Biyiklioglu, Zekeriya [1 ]
Koca, Atif [2 ]
Kantekin, Halit [1 ]
机构
[1] Karadeniz Tech Univ, Dept Chem, Fac Arts & Sci, TR-61080 Trabzon, Turkey
[2] Marmara Univ, Fac Engn, Dept Chem Engn, TR-34722 Istanbul, Turkey
关键词
Crown ether; Metallophthalocyanine; Synthesis; Cyclic voltammetry; Spectroelectrochemistry; Chromaticity diagram; METAL-FREE; SOLUBLE METALLOPHTHALOCYANINES; SUBSTITUTED COBALT; PHOTOSENSITIZERS; NICKEL(II); COMPLEXES; ZN(II); SERIES; BIS;
D O I
10.1016/j.poly.2009.04.036
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Novel Ni(II), Zn(II), Co(II) and Cu(II) phthalocyanines with four peripheral 4-[methyleneoxy(18-crown-6)] groups have been synthesized via the cyclic tetramerization of 4-[{(18-crown-6)-yl}methyleneoxy]phthalonitrile and the corresponding metal salts (NiCl2, Zn(CH3COO)(2), CoCl2 and CuCl2). The thermal stabilities of the metal-free and metallophthalocyanine compounds were determined by thermogravimetric analysis. The structures of the target compounds were confirmed using elemental analysis, IR, H-1-NMR, C-13-NMR, UV-Vis and MS spectral data. Voltammetric and in situ spectroelectrochemical measurements show that while the cobalt phthalocyanine complex gives both metal-based and ring-based redox processes, the metal-free, nickel, zinc and copper phthalocyanines show only ring-based reduction and oxidation processes. An in situ electrocolorimetric method has been applied to investigate the color of the electro-generated anionic and cationic forms of the complexes. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2171 / 2178
页数:8
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