Synthesis, spectroscopy and electrochemical properties of highly soluble fluoro containing phthalocyanines

被引:35
|
作者
Unlu, Selma [1 ]
Yarasir, Meryem N. [1 ]
Kandaz, Mehmet [1 ]
Koca, Atif [2 ]
Salih, Bekir [3 ]
机构
[1] Sakarya Univ, Dept Chem, TR-54140 Esentepe, Sakarya, Turkey
[2] Marmara Univ, Fac Engn, Dept Chem Engn, TR-34722 Istanbul, Turkey
[3] Hacettepe Univ, Fac Sci, Dept Chem, TR-06532 Ankara, Turkey
关键词
phthalocyanines; fluorine; Maldi-TOF; spectroscopy; aggregation; electrochemistry;
D O I
10.1016/j.poly.2008.05.036
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
2(3),9(10),16(17),23(24)-Tetrakis-4'-[3,5-bis-(trifluoromethyl)-phenoxy]-phthalocyanines, {M[Pc-beta(OBz-(CF3)(2))(4)]}, (M = Zn(II), Cu(II), Co(II) and Ni(II)) were synthesized and characterized by elemental analysis, FTIR, H-1 NMR, UV-Vis and MS (Maldi-TOF) spectral data. It is shown that the 4-(3,5-bis(trifluoromethyl)-phenoxy) moieties on the periphery affect the solubility, spectroscopic data and electrochemistry of the tetrakis metallophthalocyanines. The cyclic voltammetry and differential pulsed voltammetry of the complexes give well-defined redox couples in harmony with common metallophthalocyanine complexes. Electrochemical studies show that the complexes exhibit stable monoanionic M{Pc-beta-[(OBz-(CF3)(2))(4)]}(1-) dianionic M{Pc-beta-[(OBz-(CF3)(2))(4)]}(2-) and monocationic M{Pc-beta-OBz-(CF3)(2))(4)]}(1+) species during the reduction and oxidation processes. When compared with the unsubstituted analogues, the redox potentials of the complexes shifted to more positive potentials due to the electron-withdrawing fluorine groups. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2805 / 2810
页数:6
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