Syntheses, electrochemical and spectroelectrochemical properties of novel ball-type and mononuclear Co(II) phthalocyanines substituted at the peripheral and non-peripheral positions with binaphthol groups

被引:13
|
作者
Canlica, Mevlude [2 ]
Booysen, Irvin Noel [1 ]
Nyokong, Tebello [1 ]
机构
[1] Rhodes Univ, Dept Chem, Grahamstown, South Africa
[2] Yildiz Tech Univ, Dept Chem, Inorgan Chem Div, TR-34220 Istanbul, Turkey
基金
新加坡国家研究基金会;
关键词
Cobalt ball-type phthalocyanines; Non-peripheral and peripheral; phthalocyanines; Electrochemistry; Spectroelectrochemistry; GAS-SENSING PROPERTIES; CLAMSHELL;
D O I
10.1016/j.poly.2010.11.017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Mononuclear cobalt phthalocyanine (CoPc) substituted at the non-peripheral Sand peripheral positions 9 with 1,1'-binaphthy1-8,8'-diol and ball-type dinuclear Co2Pc2 substituted at the non-peripheral 10 and peripheral 11 positions with the same substituent are reported. The complexes with 1,1'-binaphthol-bridges were prepared from the corresponding phthalonitriles 4-7. The effects of the position of substituent on spectral, electrochemical and spectroelectrochemical properties of these complexes were also explored. The mononuclear complexes 8 and 9 exhibited one metal reduction, one ring reduction and one ring oxidation. The redox properties of the ball-type complexes 10 and 11 exhibited two reduction processes assigned to [((CoPc-2)-Pc-I)(2)](2-)/[((CoPc-3)-Pc-I)(2)](4-) (I), ((COPc-2)-Pc-II)(2)/[((COPc-2)-Pc-I)(2)](2-) (II) and one oxidation process assigned to [((CoPc-2)-Pc-III)(2)](2+)/(CoPc-2)-Pc-II)(2) (III). The ball-type complexes are much easier to oxidize and more difficult to reduce than the corresponding monomers 8 and 9. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:508 / 514
页数:7
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