New route to unsymmetrical phthalocyanine analogs by the use of structurally distorted subphthalocyanines

In addition to traditional uses as dyes and in photocopying devices, phthalocyanines (Pcs) are now rapidly growing in importance in many fields such as chemical sensors, electrochromism, batteries, photodynamic cancer therapy, molecular metals, photochemical hole burning, and liquid crystals. In thi...

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Published inJournal of the American Chemical Society Vol. 112; no. 26; pp. 9640 - 9641
Main Authors Kobayashi, Nagao, Kondo, Ryoko, Nakajima, Shinichiro, Osa, Tetsuo
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 01.12.1990
Amer Chemical Soc
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Summary:In addition to traditional uses as dyes and in photocopying devices, phthalocyanines (Pcs) are now rapidly growing in importance in many fields such as chemical sensors, electrochromism, batteries, photodynamic cancer therapy, molecular metals, photochemical hole burning, and liquid crystals. In this communication, the authors present a completely new method for the preparation of monosubstituted type unsymmetrical Pcs and Pc analogues, which utilizes the so-called subphthalocyanines (SubPcs).
Bibliography:istex:8FE6E78CEA5DF477BEFF447DFBDCA5AD098C3C26
ark:/67375/TPS-V4TX32SH-R
ISSN:0002-7863
1520-5126
DOI:10.1021/ja00182a034