Preparation and properties of octa-substituted phthalocyanines peripherally substituted with phenyl derivatives

被引：12

作者：

Sugimori, T ^{[1
]}

Torikata, M ^{[1
]}

Nojima, J ^{[1
]}

Tominaka, S ^{[1
]}

Tobikawa, K ^{[1
]}

Handa, M ^{[1
]}

Kasuga, K ^{[1
]}

机构：

[1] Shimane Univ, Fac Sci & Engn, Dept Mat Sci, Matsue, Shimane 6908504, Japan

来源：

INORGANIC CHEMISTRY COMMUNICATIONS | 2002年 / 5卷 / 12期

关键词：

octa-substituted phthalocyanines; Suzuki-coupling; solubility; spectroscopy;

D O I：

10.1016/S1387-7003(02)00636-6

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-Octa-substituted phthalocyanines modified with phenyl, tolyl, tert-butylphenyl, and trifluoromethylphenyl groups and their nickel(II) complexes were prepared and characterized. The phthalonitriles with the phenyl derivatives, which are precursors of the phthalocyanines, were synthesized from 4,5-dichlorophthalonitrile and phenyl boronic acids by use of Suzuki-coupling reaction. (C) 2002 Elsevier Science B.V. All rights reserved.

引用

页码：1031 / 1033

页数：3

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